- Research article
- Open Access
Antagonistic roles in fetal development and adult physiology for the oppositely imprinted Grb10 and Dlk1genes
BMC Biology volume 12, Article number: 771 (2014)
Despite being a fundamental biological problem the control of body size and proportions during development remains poorly understood, although it is accepted that the insulin-like growth factor (IGF) pathway has a central role in growth regulation, probably in all animals. The involvement of imprinted genes has also attracted much attention, not least because two of the earliest discovered were shown to be oppositely imprinted and antagonistic in their regulation of growth. The Igf2 gene encodes a paternally expressed ligand that promotes growth, while maternally expressed Igf2r encodes a cell surface receptor that restricts growth by sequestering Igf2 and targeting it for lysosomal degradation. There are now over 150 imprinted genes known in mammals, but no other clear examples of antagonistic gene pairs have been identified. The delta-like 1 gene (Dlk1) encodes a putative ligand that promotes fetal growth and in adults restricts adipose deposition. Conversely, Grb10 encodes an intracellular signalling adaptor protein that, when expressed from the maternal allele, acts to restrict fetal growth and is permissive for adipose deposition in adulthood.
Here, using knockout mice, we present genetic and physiological evidence that these two factors exert their opposite effects on growth and physiology through a common signalling pathway. The major effects are on body size (particularly growth during early life), lean:adipose proportions, glucose regulated metabolism and lipid storage in the liver. A biochemical pathway linking the two cell signalling factors remains to be defined.
We propose that Dlk1 and Grb10 define a mammalian growth axis that is separate from the IGF pathway, yet also features an antagonistic imprinted gene pair.
Growth during the development of multicellular organisms requires an expansion in cell number, generally accompanied by cellular specialisation, and the formation of distinct tissues and organs. There is a wealth of information about the underlying cellular processes, including the regulation of cell survival, proliferation and differentiation, but the control of growth and proportions at the level of tissues, organs and body size remains poorly understood –. The insulin-like growth factors (IGFs), Igf1 and Igf2, promote cell survival and proliferation, and mouse knockout studies show that they have a central role in controlling body size during development –. An analogous insulin/IGF growth-regulatory pathway has been demonstrated in a number of animals, including invertebrates such as Drosophila , and may exist in all animals. In mammals two genes encoding key components of the IGF pathway, Igf2 and Igf2r, are subject to regulation by genomic imprinting ,.
Imprinted genes have been the focus of much attention because they defy one of the central assumptions of Mendelian inheritance, that the two parental genomes can be regarded as equal. Genes regulated by genomic imprinting are expressed exclusively, or predominantly, from one parental allele in at least some of the sites where they are active . The pattern of allelic expression is a characteristic feature, with some imprinted genes expressed from the paternally-inherited allele, such as the genes encoding insulin-like growth factor 2 (Igf2)  and delta-like 1 (Dlk1) , and others expressed from the maternally-inherited allele, such as those encoding the insulin-like growth factor type 2 receptor (Igf2r)  and the non-coding RNA H19 ,. The growth factor receptor bound protein 10 gene (Grb10) exhibits expression from the maternal allele that is widespread in fetal tissues outside of the central nervous system (CNS), but also exhibits expression from the paternal allele within the CNS ,. Opposite imprinting of a single gene that expresses the same products in different tissues is currently unique to Grb10.
Several theories have been proposed for the evolution of imprinted genes, the most widely accepted being the parental conflict hypothesis, which was put forward before any of the imprinted genes were identified ,. It holds that paternally expressed genes will function to promote offspring growth, at the expense of maternal resources, while maternally expressed genes will limit offspring growth to provide a more even distribution of resources amongst offspring throughout the mother’s reproductive lifespan. This works for species in which offspring have access to maternal resources during at least some of their early growth period, and in which females are likely to reproduce with more than one male. Thus, the theory was proposed to apply to mammals and flowering plants, in which maternal resources are made available to growing offspring through the placenta and endosperm, respectively. The species distribution remains true, with imprinted genes identified in both mammals, (including marsupials) and angiosperms .
Paternally expressed Igf2 and maternally expressed Igf2r were two of the first imprinted genes to be identified ,. Mouse knockout studies revealed a role for Igf2 in promoting fetal growth  and for Igf2r as an inhibitor of fetal growth ,. This matched perfectly with the predictions of the parental conflict hypothesis and was made more compelling by the discovery that the Igf2r, also known as the cation-independent mannose 6-phosphate receptor (CI-MPR), acts by targeting Igf2 for lysosomal degradation ,. Indeed, the mammalian CI-MPR has a specific binding site for Igf2 that is not present in non-mammalian vertebrates, consistent with the Igf2r function having evolved together with genomic imprinting ,. The oppositely imprinted Igf2 and Igf2r genes are therefore functionally antagonistic, acting within the same biochemical pathway to regulate growth.
Over 150 imprinted genes have now been identified in placental mammals , a significant proportion having growth regulatory roles consistent with the parental conflict hypothesis ,. It should be noted that other imprinted genes have diverse functions, notably in energy homeostasis ,, or brain function and behaviour . Some of these functions are difficult to reconcile with the conflict hypothesis, particularly those affecting only post-natal aspects of physiology or behaviour , leading to the proposal of alternatives such as coadaptive evolution , which are not necessarily mutually exclusive with the parental conflict hypothesis ,. Since the discovery of the relationship between Igf2 and Igf2r there have been no other clear examples of imprinted genes with antagonistic growth functions, although oppositely imprinted transcripts at the Gnas locus have antagonistic roles in behaviour and physiology . There are also examples of changes in one imprinted gene affecting the expression of others, potentially in a network of growth regulatory imprinted genes that includes Igf2, Cdkn1c (p57 KIP2) and Dlk1 . Most notably, both IGF2 and the maternally expressed cell cycle inhibitor CDKN1C can contribute to the overgrowth disorders seen in Beckwith-Wiedemann syndrome  and there is evidence that changes in Igf2 expression can influence expression of Cdkn1c .
We have previously shown that Grb10 has multiple roles. The maternal Grb10 allele acts as an inhibitor of both fetal and placental growth, with mice inheriting a null allele of Grb10 through the maternal line (Grb10 m/+) being born approximately 25% to 40% larger than their wild type littermates ,–. As adults Grb10 m/+animals are lean, with increased muscle mass, elevated insulin signalling and an enhanced ability to clear a glucose load ,–. Furthermore, expression of the maternal Grb10 alleles in both mother and offspring have complementary roles that appear to be required for optimal offspring growth and body proportions . Mice with the paternally-inherited allele of Grb10 knocked out (Grb10 +/p) exhibit normal growth and physiology, but as adults display increased social dominance, consistent with CNS-specific expression from the paternal Grb10 allele . Grb10 is an adaptor protein capable of interacting with numerous intracellular signalling molecules, notably including receptor tyrosine kinases and mammalian target of rapamycin (mTOR) –. Biochemical interactions of Grb10 with the insulin receptor (Insr) and with Igf1r are well established . While there is good evidence that Grb10 acts as an inhibitor of insulin signalling in some contexts in vivo ,,, mouse genetic experiments indicate that Grb10 influences fetal and placental growth through a pathway independent of either Igf2 , Igf1r or Insr (unpublished data). The signalling pathway through which Grb10 influences growth is currently unknown.
In contrast to the Grb10 m/+ knockout phenotype, mice inheriting a knockout of the paternal Dlk1 allele (Dlk1 +/p) display significant growth retardation on the day of birth, and as adults are predisposed to accumulate excess adipose . Transgenic mice overexpressing Dlk1 from an adipose-specific promoter exhibit reduced adipose mass, impaired glucose tolerance and decreased insulin resistance ,. The adiposity phenotypes of the Dlk1 knockout and transgenic mice are consistent with abundant evidence that Dlk1, also known as preadipocyte factor-1 (pref-1), is an important regulator of adipogenesis . Enhanced fetal growth of Grb10 m/+ mice is associated with expansion of the labyrinthine portion of the placenta , whereas placental labyrinth volume is reduced in Dlk1 +/p mice . As adults, Grb10 m/+ mice have increased muscle mass, due to an increase in myofiber number ,, while Dlkl −/− animals exhibit reduced muscle mass associated with a delay in myogenesis during fetal development . Here, we test the hypothesis that the oppositely imprinted Grb10 and Dlk1 genes have antagonistic roles in a common genetic pathway. Analyses of growth and physiological phenotypes of Grb10 m/+/Dlk1 +/p double knockout animals support this hypothesis. Our data indicate that, in addition to the IGF pathway, a second mammalian fetal growth regulatory axis exists in which oppositely imprinted genes have evolved roles consistent with the parental conflict hypothesis.
Grb10 m/+/Dlk1 +/p double knockout mice have a fetal overgrowth phenotype similar to that of Grb10 m/+single knockout mice, including increased cell proliferation along with altered lengths of S- and G2-phases of the cell cycle
To investigate growth phenotypes resulting from ablation of the Grb10 and Dlk1 genes, fetal and placental wet weights together with placental efficiencies were analysed at different gestational stages (Figure 1 and Additional file 1: Figure S1). At embryonic day (E)12.5 Grb10 m/+and Grb10 m/+/Dlk1 +/p fetuses were significantly heavier than wild type and also Dlk1 +/p littermate controls, with no statistically significant differences seen in placental mass (see Additional file 1: Figure S1A,C). Both Grb10 m/+ and Grb10 m/+/Dlk1 +/p fetuses and placentae were significantly enlarged at E14.5, again in comparison with both wild type and Dlk1 +/p controls (Figure 1A,D). The same trend was observed at E17.5, with both Grb10 m/+and Grb10 m/+/Dlk1 +/p fetuses exhibiting significant overgrowth when compared to wild type and Dlk1 +/p fetuses, but in the case of placentae statistically significant overgrowth was observed only in comparison to Dlk1 +/p littermates (see Additional file 1: Figure S1B,C). Determination of fetal/placental weight ratios as a measure of placental efficiency revealed significantly improved efficiencies for both Grb10 m/+and Grb10 m/+/Dlk1 +/p placentae at E17.5 but not at E12.5 or E14.5 (Figure 1B,D). We previously found that Grb10 m/+ neonates (on the day of birth) exhibited disproportionate liver enlargement ,, and here we identified significant overgrowth in wet weights and relative weights of both Grb10 m/+and Grb10 m/+/Dlk1 +/p E17.5 livers (Figure 1C,D).
The tissue overgrowth observed from E12.5 onwards in both Grb10 m/+and Grb10 m/+/Dlk1 +/p fetuses might be associated with either, or both, increased cell size and cell number. To investigate the cellular basis of tissue overgrowth we first analysed proliferation rates of primary mouse embryonic fibroblasts (PMEFs) derived from E14.5 fetuses. PMEFs were seeded at the same initial density and monitored over a period of 11 days, revealing that Grb10 m/+and Grb10 m/+/Dlk1 +/p cells were hyperproliferative (Figure 2A). Note that at 24 hours, the first time-point cells were counted after initial seeding, there was essentially no difference in cell numbers. Statistical analysis of areas under the growth curves showed that accumulation of PMEFs derived from both Grb10 m/+and Grb10 m/+/Dlk1 +/p fetuses was significantly increased in comparison with those derived from wild type and Dlk1 +/p fetuses (Figure 2B,C). No statistically significant deviation from wild type growth was shown by Dlk1 +/p cells, although they did exhibit a consistent trend to proliferate at a slightly lower rate than wild type cells.
Fluorescence activated cell sorting (FACS) was employed to examine the basis for the hyperproliferative phenotype of Grb10 m/+and Grb10 m/+/Dlk1 +/p E14.5 PMEFs and to investigate the possibility of cellular hypertrophy. No deviations from wild type were found in the ranges of cell sizes upon FACS analysis of Dlk1 +/p, Grb10 m/+and Grb10 m/+/Dlk1 +/p cells from E14.5 fetuses, suggesting that the observed overgrowth phenotypes in Grb10 m/+and Grb10 m/+/Dlk1 +/p fetuses were not the result of cell hypertrophy (see Additional file 2: Figure S2A,B). In contrast, analysis of cell cycle stages revealed statistically significant increases in the proportion of Grb10 m/+and Grb10 m/+/Dlk1 +/p cells in G2-phase compared to Dlk1 +/p cells, along with decreased numbers of Grb10 m/+and Grb10 m/+/Dlk1 +/p cells in S-phase compared to wild type (Figure 3A-D). To eliminate potential confounds associated with cell culture, FACS analysis was also undertaken using freshly derived single cell suspensions from E11.5 fetuses. We again found no changes in cell size distribution (see Additional file 2: Figure S2C,D). Also consistent with data from PMEFs, Grb10 m/+and Grb10 m/+/Dlk1 +/p- fetuses showed significantly higher percentages of cells in G2-phase of the cell cycle, compared to both wild type and Dlk1 +/p- fetuses, with decreased numbers in S-phase, although this time statistically significant only in comparison to Dlk1 +/p fetuses (Figure 3E-H).
At birth and as adults Grb10 m/+and Grb10 m/+/Dlk1 +/p mice share characteristic changes in body weight and proportions that distinguish them from wild type and Dlk1 +/panimals
We next analysed body weight, proportions and selected histological features of mice at post-natal stages from the day of birth (neonates) to nine months of age. As expected, neonatal Dlk1 +/p knockout mice were significantly smaller than wild type mice whilst Grb10 m/+ knockout mice were significantly overgrown (Figure 4A,G). Grb10 m/+/Dlk1 +/p double knockout neonates also displayed an overgrowth phenotype, being significantly heavier than wild type and Dlk1 +/p animals but not significantly different from Grb10 m/+ single knockouts. Analysis of organ wet weights showed that liver, lung and heart were each significantly enlarged in both Grb10 m/+and Grb10 m/+/Dlk1 +/p double knockout neonates (see Additional file 3: Figure S3), and when expressed as a proportion of body weight, heart (Figure 4F,G) and lung (Figure 4E,G) were essentially in proportion with total body weight, with liver disproportionately enlarged (Figure 4C,G), as previously shown for Grb10 m/+ mice ,. The wet weights of brain and kidney exhibited no significant differences between the genotypes (see Additional file 3: Figure S3) and consequently, as a proportion of body weight, appeared enlarged in Dlk1 +/p neonates and reduced in Grb10 m/+ neonates (Figure 4B,D,G). In Grb10 m/+/Dlk1 +/p double knockout neonates relative weights of both brain and kidney were significantly different to those of Dlk1 +/p but not wild type or Grb10 m/+ animals. Lungs of Dlk1 +/p animals were significantly enlarged in comparison to wild type (Figure 4E,G).
To investigate if the identified body weight differences detected at birth would persist in postnatal life we next analysed wild type, Grb10 m/+, Dlk1 +/p and Grb10 m/+/Dlk1 +/p mice at one week, three to six months and more than six to nine months of age. At one week, persistent overgrowth was seen in Grb10 m/+ (compared to wild type and Dlk1 +/p) and Grb10 m/+/Dlk1 +/p (compared to Dlk1 +/p) knockout mice (Figure 5A,D). Wet weights of the Grb10 m/+and Grb10 m/+/Dlk1 +/p livers were significantly elevated at this stage (Figure 5B,D). However, when liver weights were expressed as percentages of the total body weights, no significant differences between the genotypes were found, indicating a shift from the disproportionate overgrowth seen at birth to a proportional increase in liver weight in Grb10 m/+and Grb10 m/+/Dlk1 +/p mice (Figure 5C,D). At three to six and more than six to nine months of age, body weights were again compared, along with wet weights and relative weights of selected organs (data summarised in Table 1). Only males three- to six-months old showed a significant difference in body weight, with Grb10 m/+ being heavier than wild type and Dlk1 +/p animals. Several of the analysed organs showed significant differences in weights between genotypes and there was a notable tendency for Grb10 m/+and Grb10 m/+/Dlk1 +/p mice to group together. These differences included increased pancreas weights and decreased kidney weights in Grb10 m/+and Grb10 m/+/Dlk1 +/p mice that were consistent between males and females of the same age and/or between animals at the two different ages. The livers of Grb10 m/+and Grb10 m/+/Dlk1 +/p mice were significantly smaller than those of Dlk1 +/p animals in males three- to six-months old and exhibited a similar trend in the other adult cohorts.
Grb10 m/+and Grb10 m/+/Dlk1 +/p mice share age-related changes in liver histology that distinguish them from wild type and Dlk1 +/panimals
The differences in liver weight and proportions that we observed in Grb10 m/+and Grb10 m/+/Dlk1 +/p mice from E17.5 to adult stages were accompanied by striking changes in histology (Figure 6 and Additional file 4: Figure S4). In comparisons of tissue sections stained with haematoxylin and eosin (H & E) for all four genotypes, no obvious differences were found in E14.5 fetal liver (data not shown); however, the presence of numerous clear, round spaces was noted in neonatal Grb10 m/+ and Grb10 m/+/Dlk1 +/p livers (see Additional file 4: Figure S4A) which were also present in approximately half of the examined Grb10 m/+ and Grb10 m/+/Dlk1 +/p livers from one-week-old mice (data not shown). In contrast, Grb10 m/+ and Grb10 m/+/Dlk1 +/p livers from three-month-old male mice were essentially indistinguishable from wild type, but at this stage Dlk1 +/p livers were found to have an abnormal accumulation of larger clear, round spaces (see Additional file 4: Figure S4B). Oil Red O staining of cryosections revealed that Grb10 m/+ and Grb10 m/+/Dlk1 +/p neonatal livers had increased staining compared with wild type and Dlk1 +/p samples (Figure 6A,C,D), indicating the accumulation of lipid in a manner consistent with the appearance of clear spaces in H & E stained sections (see Additional file 4: Figure S4A). Similarly, Oil Red O staining of adult liver cryosections revealed marked lipid droplet accumulation in Dlk1 +/p but not in wild type, Grb10 m/+ and Grb10 m/+/Dlk1 +/p (Figure 6B), again in keeping with the observation of clear spaces in H & E stained sections (see Additional file 4: Figure S4B).
Dual energy X-ray absorptiometry analysis of adult body composition shows both Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice have increased lean tissue content, while Dlk1 +/pmice have a higher adipose proportion and elevated serum triglycerides
To further evaluate body proportions among mice of the four different genotypes, we performed dual energy X-ray absorptiometry (DXA) analyses of adult males (Figure 7) and females (see Additional file 5: Figure S5). No significant differences in bone mineral density (BMD) and bone mineral content (BMC) were identified in male mice, indicating no major changes in bone quantity and composition (Figure 7A,B,G). Female Dlk1 +/p mice had significantly reduced BMC compared to wild type controls, and this was the only difference in BMC or BMD detected (see Additional file 5: Figure S5A,B,G). Lean tissue content was significantly increased for Grb10 m/+ male mice when compared to wild type and Dlk1 +/p mice and also in Grb10 m/+/Dlk1 +/p mice when compared to Dlk1 +/p (Figure 7C,G). Grb10 m/+ female mice also had significantly higher content of lean tissue, but only when compared to Dlk1 +/p (see Additional file 5: Figure S5C,G). When expressed as a percentage of the total, lean mass of Grb10 m/+ mice was significantly increased compared to Dlk1 +/p mice, both in males (Figure 7E,G) and females (see Additional file 5: Figure S5E,G). No significant differences were observed in absolute values for adipose tissue content of males (Figure 7D,G) or females (see Additional file 5: Figure S5D,G); however, when expressed as a percentage of total body mass, adipose tissue content was significantly increased in Dlk1 +/p compared to Grb10 m/+ for both males (Figure 7E,G) and females (see Additional file 5: Figure S5F,G). In support of this observation, serum triglyceride concentration measured in adult males was found to be significantly elevated in Dlk1 +/p mice when compared to Grb10 m/+ mice (Figure 7H,I) and the wet weight of both gonadal and renal adipose depots was significantly increased in females at three to six months of age (Table 1). Changes in lean:adipose body proportions were not accompanied by any obvious changes in white adipose tissue histomorphometry (see Additional file 6: Figure S6) or food consumption (see Additional file 7: Figure S7). Dlk1 knockout mice derived independently of those used in this study were shown to exhibit transient adipocyte hypotrophy , with mean adipocyte size being reduced in the analysed adipose depots at six weeks of age, but not at sixteen weeks. Our adipose measurements were carried out on a cohort of three-month-old animals and transient adipocyte hypotrophy in younger Dlk1 +/p animals has not been excluded.
Both Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice exhibit enhanced glucose clearance compared to Dlk1 +/pmice
Previous studies have shown that in Grb10 m/+ knockout mice increased lean:adipose body proportions and elevated insulin signalling were associated with improved glucose tolerance and insulin sensitivity ,,. Conversely, transgenic mice overexpressing Grb10 exhibited impaired glucose tolerance and insulin resistance ,. There are no published studies of glucose or insulin tolerance in Dlk1 knockout mice, but transgenic mice overexpressing Dlk1 exhibit reduced adipose deposition, glucose intolerance and insulin resistance ,. Consequently, we performed glucose tolerance tests (GTTs) on mice of all four genotypes used in this study (Figure 8). In all cases, following intraperitoneal injection of fasted animals with a bolus of glucose, blood glucose concentration showed an initial sharp rise followed by a gradual decline, consistent with insulin mediated glucose uptake. Compared to wild type controls, curves plotted for Dlk1 +/p mice showed impaired glucose clearance, while those for Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice showed enhanced glucose clearance, both for males (Figure 8A) and females (Figure 8B). Comparisons of the area under each curve revealed significant differences in glucose clearance between Dlk1 +/p and both Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice, again for both males and females (Figure 8C,D, E).
Neonatal Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice have thickened lung epithelia compared with wild type and Dlk1 +/pmice, whereas no differences were detected in histology of kidney and pancreas, or in skeletal morphology
Following the previous reports of neonatal death in a minority of Grb10 m/+ mice that was associated with blood filled lung alveoli  and pulmonary defects noted in Dlk1 knockout mice , we performed histological analyses of neonatal lungs (Figure 9A). Measurements of lung epithelial walls showed that both Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice had significantly thicker epithelial walls when compared to either Dlk1 +/p or wild type animals (Figure 9B,C). Similar morphometric analysis of adult lung showed no differences between any of the four genotypes, indicating that the thickened lung epithelial wall phenotype did not persist into adulthood (data not shown).
Skeletal malformations were previously reported in Dlk1 knockout mice  and the soluble form of Dlk1, fetal antigen-1 (FA1), has been identified as a novel endocrine factor regulating chondrocyte differentiation in vitro , as well as bone and adipose mass in vivo ,. Our Grb10 knockout mice incorporate a β-galactosidase reporter gene within the Grb10 locus that we have previously found to recapitulate endogenous Grb10 expression patterns in both fetal and adult tissues ,–, although expression can be low at specific sites where Grb10 appears to be regulated by STAT5 . Here we employed LacZ staining to examine Grb10 expression in neonatal bones, with expression readily detected in growth plates of Grb10 m/+ and Grb10 m/+/Dlk1 +/p animals, indicating a possible role for Grb10 in growth of long bones during skeletogenesis (see Additional file 8: Figure S8A). However, staining of skeletal preparations of mice of all four genotypes with Alcian Blue and Alizarin Red to highlight cartilage and bone, respectively, revealed no obvious skeletal defects (see Additional file 8: Figure S8B), including those previously described for Dlk1 knockout mice. This difference in the mice used by ourselves and Moon et al.  could be due to the precise nature of the engineered mutations or their maintenance on different strain backgrounds. Nevertheless, the observed expression of Grb10 in the growth plate of long bones is consistent with a role in skeletogenesis, which could contribute to the growth phenotype of Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice.
Use of the LacZ insert at the Grb10 locus in our knockout mice revealed that the maternal Grb10 allele is expressed in adult kidney, most obviously in the proximal tubules (see Additional file 9: Figure S9). This, together with the observation of altered kidney proportions in Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice (Figure 4 and Table 1), prompted us to examine adult kidneys in more detail. However, we detected no obvious differences in histology of adult kidney among animals of the four genotypes used in this study (see Additional file 9: Figure S9) and in all cases there was no evidence of compromised kidney function as judged by analysis of protein content of urine samples collected from mice at three months of age (data not shown). The observed expression pattern may be relevant to the tumour suppressor role proposed for Grb10 in small cell renal cell carcinoma , a prevalent adult kidney cancer thought to arise predominantly from the proximal tubule .
Paternally-expressed Igf2 and maternally-expressed Igf2r were the first imprinted genes to be identified and their opposite growth regulatory roles were quickly recognised to fit with predictions of the parental conflict hypothesis ,. Genetic crosses between females heterozygous for an Igf2r knockout allele and males heterozygous for an Igf2 knockout allele revealed that the growth inhibitory function of Igf2r could be attributed entirely to an antagonistic interaction with Igf2 ,. This conclusion derives from the observation that the growth of Igf2r m/+/Igf2 +/p double knockout offspring was indistinguishable from that of Igf2 +/p knockout littermates. Although not a prerequisite of the hypothesis, the fact that the opposing functions of the two genes were enacted through direct interaction of their gene products made the case for a parental ‘tug-of-war’ even more compelling ,. Here, we have carried out a test for epistasis between Grb10 and Dlk1, oppositely imprinted genes with contrasting effects on fetal growth, adiposity and glucose homeostasis ,,,–,. We carried out detailed analyses of wild type, Grb10 m/+ and Dlk1 +/p single knockout, and Grb10 m/+/Dlk1 +/p double knockout mice for features related to growth and metabolic phenotypes previously established as characteristic of either single knockout. Quantitative phenotyping consistently revealed that Grb10 m/+/Dlk1 +/p double knockout and Grb10 m/+ mice closely resemble each other, such that they are never significantly different, and are distinct from wild type and Dlk1 +/p mice. Distinguishing phenotypic characters include growth during early life, cell cycle profiles, tissue proportions, glucose regulated metabolism and specific histological features, notably lipid storage in the liver. These findings support the notion that Grb10 and Dlk1 act in the same genetic pathway, with Dlk1 acting upstream of Grb10. In order to promote growth Dlk1 must inhibit Grb10, which is in turn a growth inhibitor (Figure 10).
Disruption of the maternal Grb10 allele has previously been shown to result in fetal and placental overgrowth ,–. Grb10 m/+ mice are at birth around 25% to 40% larger than wild type littermates, with significant differences in weight first apparent in the fetus at E12.5 and in the placenta at E14.5. In addition, the enlarged Grb10 m/+ placenta was found to be significantly more efficient than the wild type placenta from E17.5 . In the present study, the overgrowth phenotype of Grb10 m/+ mice was similar in both magnitude and timing to that previously observed, with significantly increased placental efficiency again manifest from E17.5. At the three gestational stages examined Dlk1 +/p fetal and placental weights were consistently lower than those of wild type littermates, but not statistically significantly so. Similar data were reported recently for a different Dlk1 knockout strain ; however, the small decreases in fetal weight are likely to have biological significance as our Dlk1 +/p mice were at birth significantly smaller (approximately 20% by weight) than their wild type littermates, again as previously reported . With the exception of E12.5 placentae, weights of Dlk1 +/p offspring were always significantly lower than those of both Grb10 m/+ and Grb10 m/+/Dlk1 +/p offspring. Importantly, Grb10 m/+ and Grb10 m/+/Dlk1 +/p offspring closely resembled each other and were never significantly different.
The close resemblance of Grb10 m/+ and Grb10 m/+/Dlk1 +/p offspring was also apparent in comparisons of tissue proportions. We have previously noted disproportionate liver overgrowth in Grb10 m/+ pups at birth , and here this was seen in both Grb10 m/+ and Grb10 m/+/Dlk1 +/p offspring at birth and at E17.5. At these stages liver was proportionate to body size in Dlk1 +/p mice, whereas kidney was significantly enlarged compared to wild type controls. In both Grb10 m/+ and Grb10 m/+/Dlk1 +/p the kidneys of neonates were significantly reduced as a proportion of body weight. Brain weight remained essentially unchanged in neonates of all four genotypes, such that it was enlarged in proportion to body weight in Dlk1 +/p and proportionately small in Grb10 m/+ neonates. We have noted this effect before in Grb10 m/+ neonates, which correlates with the lack of expression from the maternal Grb10 allele in the developing brain ,. This is consistent with the Grb10/Dlk1 growth regulatory pathway having a brain ‘sparing’ role , under conditions in which fetal growth is restricted, notably when nutrients are limiting. The underlying mechanisms are poorly understood but in Drosophila sparing of the CNS under starvation conditions has been linked with tissue-specific modifications in PI3K/TOR signalling . The TOR (mTOR in mammals) pathway is highly conserved, with key roles in nutrient sensing and growth factor signalling ,. Thus, a brain sparing role for Grb10 through the established interaction with mTOR , is plausible.
Growth rates of PMEFs derived from E14.5 fetuses showed differences between genotypes that were in keeping with the observed fetal growth phenotypes. Thus, while Dlk1 +/p fibroblasts proliferated slowly (though not significantly so) compared to wild type, both Grb10 m/+ and Grb10 m/+/Dlk1 +/p fibroblasts exhibited a significantly higher proliferation rate. FACS analyses of E14.5 fetus-derived fibroblasts revealed for both Grb10 m/+ and Grb10 m/+/Dlk1 +/p cells a significant reduction in the number of cells in S-phase of the cell cycle, with a concomitant increased number in G2. The same FACS profile was observed for cells derived from disaggregated E11.5 fetuses. These FACS data, together with the fibroblast proliferation rates, indicate that the enhanced growth of Grb10 m/+ and Grb10 m/+/Dlk1 +/p fetuses is associated with more rapid progress through S-phase. Grb10 overexpression in an in vitro leukaemia model was associated with increased cell numbers in S-phase, increased proliferation and decreased apoptosis , suggesting that its role in cell cycle regulation is highly context dependent. The FACS data from E11.5 fetal cells indicates that the cell cycle changes we observed are physiologically relevant and, logically, manifest before any significant effect on fetal weight can be detected (at E12.5). This is analogous to the early detection of cell cycle changes in Igf2 knockout mice (Igf2 +/p) , but whereas the major cell cycle changes in Igf2 +/p fetuses were focused within a narrow developmental window (E9-E10), our PMEF data suggest that altered cell cycle regulation in Grb10 m/+ and Grb10 m/+/Dlk1 +/p fetuses extends at least until E14.5.
Body and tissue weights were analysed at three further post-natal stages: one week, three to six months and more than six to nine months. Weights and tissue proportions were consistently similar between Grb10 m/+ and Grb10 m/+/Dlk1 +/p animals and were unlike those of wild type and/or Dlk1 +/p animals. Notably, adult Dlk1 +/p mice exhibited a tendency to accumulate excess adipose that is in keeping with a previous report , although in that case increased adiposity was revealed after placing the mice on a high fat diet. A third Dlk1 knockout strain, maintained on a regular diet and consistently having a reduced body weight (measured between 7 and 42 weeks of age) in comparison with wild type controls, exhibited no significant changes in the weights of several adipose depots . In contrast, Grb10 m/+ and also Grb10 m/+/Dlk1 +/p adults tended to have greater lean mass, although this was not as pronounced as in previous studies of Grb10 m/+ animals ,–, which we suspect can be attributed to the genotype of the Grb10 heterozygote mothers used in different crosses. Here, the females used as mothers were themselves Grb10 m/+ animals and, therefore, large at birth and lean as adults, whereas the Grb10 +/p mothers used in previous studies were effectively wild type in growth and physiology. This needs to be verified but is interesting because it indicates that the environment provided to offspring by Grb10 m/+ and Grb10 +/p mothers during pregnancy and/or the post-natal suckling period is different and has a long-standing effect on offspring physiology. This is consistent with a role for Grb10 in developmental programming of offspring growth and metabolism, as previously suggested by ourselves  and others ,.
The more subtle change in lean:adipose proportions seen in Grb10 m/+ and Grb10 m/+/Dlk1 +/p animals in this study is also noteworthy when considering that animals of both genotypes exhibited an enhanced ability to clear a glucose load similar in magnitude to that previously reported in Grb10m/+ mice ,. Previous studies have shown that Grb10 m/+ mice exhibit elevated insulin signalling in muscle and white adipose tissue (WAT), but it was unclear whether this made a major contribution to their improved glucose tolerance because they also had significantly increased lean/muscle mass ,–. Here, the clear improvement in glucose tolerance with a less dramatic increase in muscle mass suggests that enhanced insulin signalling does have a major effect on glucose homeostasis in Grb10 m/+ (and Grb10 m/+/Dlk1 +/p) animals. This conclusion is supported by a recent report showing that cultured primary myotubes derived from Grb10−/− mice exhibit enhanced glucose uptake and insulin signalling .
The changes in adiposity in Dlk1 +/p (increased), Grb10 m/+ and Grb10 m/+/Dlk1 +/p (both decreased) animals were reflected in serum triglyceride levels and in histological changes seen in liver at different developmental stages. Grb10 m/+ and Grb10 m/+/Dlk1 +/p animals had at birth disproportionately enlarged livers with a high lipid content compared to wild type and Dlk1 +/p livers. At one week of age, evidence of high lipid content could be seen in only around 50% of Grb10 m/+ and Grb10 m/+/Dlk1 +/p livers, consistent with the down-regulation of Grb10 in liver and other tissues post-natally . In adulthood, Grb10 m/+ and Grb10 m/+/Dlk1 +/p livers had a low lipid content and weighed less than those of wild type controls, whereas Dlk1 +/p livers had a high lipid content. Dlk1 has established roles in influencing proliferation and differentiation of several tissues, including adipose ,– and skeletal muscle . The developmental mechanisms through which Grb10 regulates growth and tissue proportions are less well understood, although recent evidence indicates that primary cultures of muscle cells from Grb10−/− mice exhibit increased rates of proliferation and differentiation . Our data indicate roles for both Grb10 and Dlk1 in regulating adipose distribution that is consistent with the recognised role for Dlk1 in inhibiting adipocyte differentiation. It will be important in the future to focus greater attention on Grb10 as a potential regulator of the balance between cell proliferation and differentiation, not least in the tissues where it has an established physiological role, including adipose ,,, skeletal muscle ,, and now liver.
The molecular basis of the interaction between Grb10 and Dlk1 is currently unknown and may not be direct as in the case of Igf2 and Igf2r. Since our genetic experiments indicate that Dlk1 operates upstream of Grb10 (Figure 10), the most parsimonious prediction would be that Dlk1 acts as a ligand for a cell surface receptor that in turn interacts with Grb10. The Grb10 adaptor protein is capable of interacting with many receptors and downstream signalling components, including mTOR –. Conversely, the receptor(s) for Dlk1 are unknown. Although Dlk1 shares amino acid sequence homology with members of the Delta/Serrate family of ligands it lacks the motifs known to be important for interaction with the Notch family of receptors . Despite this there is in vitro evidence that Dlk1 may act as an inhibitor of the NOTCH1 receptor, but also that it can influence other signalling pathways, including ERK/MAPK, AKT/PI3K and mTOR ,– signalling. Thus, there is ample scope for Dlk1 and Grb10 to interact in key growth factor signalling pathways. Further work on our single and double knockout mouse models will be required to establish the molecular pathway between Dlk1 and Grb10.
Based on the accumulated evidence we propose that Grb10 and Dlk1 may define a mammalian growth-regulatory axis that is separate from the IGF pathway, yet is similar in having as key components a pair of oppositely imprinted genes with antagonistic functions. This is only the second clear example of a pair of imprinted genes with such antagonistic roles, after Igf2 and Igf2r.
The Grb10Δ2-4 knockout mouse strain (herein referred to as Grb10 m/+) was generated as described in  and stocks maintained on a mixed C57BL/6 x CBA genetic background. Dlk1Δ1-3 +/p knockout mice (herein Dlk1 +/p) were generated as described in Raghunandan et al.  and stock maintained on a C57BL/6 genetic background. Both strains were housed as previously described . In order to generate experimental animals, Grb10 m/+females were crossed with Dlk1 +/p male mice, thereby taking advantage of the imprinted status of each gene to generate in equal proportions mice of four genotypes; wild type (WT or Grb10 +/+; Dlk1 +/+), Grb10 m/+and Dlk1 +/p single knockouts, and Grb10 m/+/Dlk1 +/p double knockouts. Siblings of each genotype were used in all subsequent analyses, thereby controlling for age and genetic background, with data from males and females analysed separately for most comparisons. Placentae and fetuses were collected and weighed at 12, 14 and 17 days after the observation of a cervical plug, designated embryonic days E12.5, E14.5 and E17.5, respectively. Animals were genotyped by PCR using primers described previously for both Grb10  and Dlk1  alleles. All experiments were carried out under license from the United Kingdom Home Office.
Tissue dissection and histological procedures
Mice were humanely culled and their total body weights recorded, as well as organ weights following dissection. Organs destined for wax embedding were fixed in 4% (w/v) paraformaldehyde (PFA) in PBS at 4°C overnight, processed using a Leica TP 1020 machine, and sections cut at approximately 6 μm using a microtome (Leica RM 2155) prior to staining with haematoxylin and eosin (H & E) or periodic acid – Schiff stain, as previously described . Organs destined for cryosectioning were fixed for 30 minutes in 2% PFA, 0.2% glutaraldehyde in PBS, transferred into ice cold 30% (w/v) sucrose and incubated at 4°C overnight, then embedded in optimal cutting temperature (OCT) compound (VWR International, Lutterworth, UK) and sections cut at approximately 10 μm using a cryostat (CM1850; Leica). For lipid staining a working solution of Oil Red O (Fisher Scientific, Loughborough, UK) in 60% isopropanol was heated and stirred at 100°C for five minutes and then filtered using 25 μm Whatman filter paper (Camlab, Cambridge, UK), first when hot and then again when cool. Cryosections were air-dried and rinsed with 60% isopropanol prior to incubating in Oil Red O solution for 15 minutes. Sections were then rinsed with 60% isopropanol and gently washed under running tap water until clear. Slides were counterstained with Mayer’s haematoxylin or Light Green (Lamb) for 30 seconds, washed under running tap water for approximately three minutes and mounted in gel mounting medium (VectaShield, Vector Laboratories, Peterborough, UK). ImageJ software was used to calculate the liver surface stained by Oil Red O. First, the colour channels in the picture were split and the green channel was chosen for analysis. Next, the threshold was adjusted so the highlighted area most accurately resembled the red staining in the original picture and the highlighted area was calculated. Cryosections for β-galactosidase gene expression analysis were fixed for 30 minutes in 4% PFA and then incubated in 1 mg/ml 5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside (X-gal) in stain base (5 mM K4Fe(CN)6, 5 mM K3Fe(CN)6.3H2O, 2 mM MgCl2, 0.01% (w/v) sodium deoxycholate, 0.02% (v/v) Igepal CA-630 in PBS) overnight at 37°C. Following incubation, sections were rinsed in PBS and stained with Nuclear Fast Red (Vector Laboratories). Stained sections were viewed under a Nikon Eclipse E800 compound microscope and pictures taken using a Nikon digital Sight DS-U1 camera operated with NIS Elements D 2.30 software.
Pictures of lung, kidney and adipose tissue sections from three-month-old male mice were captured at 200x magnification and overlaid with an 8 x 4 grid. The whole section was divided into 32 squares of equal size and the same five specific squares from each slide were used for morphometric measurements or cell counting.
Alcian blue/Alizarin red staining
For skeletal analysis, we adapted the method of McLeod . Skin and dense organs were removed from carcasses, fixed in 100% ethanol for three days and then in acetone for one day. Skeletons were washed in water purified using a Milli-Q Biocel (Millipore, Billerica, MA, USA) for several minutes before staining in colour solution (1 part 0.3% Alcian Blue in 70% ethanol: 1 part 0.1% Alizarin Red in 95% ethanol: 1 part glacial acetic acid: 17 parts 70% ethanol) for three days at room temperature. Skeletons were then submerged in purified water for several minutes and soft tissues were cleared in 1% KOH until the skeleton was visible. They were then transferred serially into 50% and 80% glycerine for approximately 24 hours each, and finally transferred into 100% glycerine.
Dual energy X-ray absorptiometry and measurement of blood serum triglyceride levels
Carcasses from mice between three to nine months of age were analysed by DXA using a PIXImus scanner (Lunar, Madison, WI, USA) with small-animal software, essentially as previously described . Readouts were recorded of total body area, lean and adipose tissue weight, bone mineral density and bone mineral content. Lean and adipose tissue weights were expressed as percentages of total body weight before performing statistical analysis. Triglyceride levels were measured in three-month-old male mice fasted for 16 hours prior to the start of the experiment. Between 50 μl and 100 μl of blood was obtained from the tail tip. Triglyceride levels were measured using a Triglyceride Assay Kit (Cayman Chemical Company, Ann Arbor, MI, USA) according to manufacturer’s instructions.
Food consumption, glucose tolerance tests and proteinurea assays
Food consumption measurements and also glucose tolerance tests performed to assess whole body glucose clearance were carried out as previously described  on mice between three to six and more than six to nine months of age. Food consumption was calculated in direct proportion to body mass, and also using the ratio of 2/3x body mass as a scaling component to take account of basal metabolic rate which varies as a function of body mass . Assays of urine for the appearance of elevated protein levels as a measure of impaired kidney function were performed using SDS-PAGE, essentially as described previously  on samples from male mice at three months of age.
Primary mouse embryonic fibroblast analyses
PMEF cells were derived from E14.5 embryos and maintained according to methods described in . Cell number per 1 ml was determined using a haemocytometer. Following the third passage, 1 x 104 cells were seeded per well of a standard 24-well plate and an initial count of the attached cells was taken 24 hours later. After this point cells from four wells were counted every 48 hours over an 11 day period in three separate experiments and the results used to calculate mean values. Cell growth was calculated as a percentage of the initial seeding density.
Propidium iodide staining of whole embryo cell extracts and primary mouse embryonic fibroblasts for fluorescence activated cell sorting analysis
Analysis of cells from disaggregated embryos was carried out essentially as described in . Embryonic day 11.5 (E11.5) embryos were dissected from the uterus and washed several times with filtered, ice cold PBS. Embryos were disaggregated using a pestle inside a 1.5 ml tube, gently resuspended and centrifuged for 10 minutes at 500 g. Cell resuspension in ice cold PBS was repeated twice, with an intervening centrifugation, and then cells were gently dissociated by filtering through a 40 μm nylon cell strainer (BD Biosciences, San Jose, CA, USA). PMEFs reaching approximately 70% confluency were washed with PBS, trypsinised by adding 1 ml of 0.25% trypsin-ethylenediaminetetraacetic acid (Fisher Scientific, Loughborough, UK) solution per 25 cm2 and washed twice in ice cold PBS.
Embryonic cell suspensions and PMEFs were stained for 30 minutes at 37°C in propidium iodide solution (50 μg/ml propidium iodide, 100 μg/ml RNAse A, 0.1% Igepal CA-630 and 50 μg/ml trisodium citrate in PBS). Stained cells were then washed in PBS and 100,000 fluorescence events were collected using a FACS Canto instrument (BD Biosciences) at the excitation wavelength of 488 nm and an emission wavelength of 600 nm. Cells were analysed for cell size (forward scatter versus side scatter) and cell cycle position (propidium iodide concentration). Data were analysed using FlowJo software (v7.6, FlowJo Software, Ashland, OR, USA).
GraphPad Prism (v5, GraphPad Software, La Jolla, CA, USA) was used for statistical analysis. Results were subject to one-way analysis of variance (ANOVA), and a post-hoc Tukey test was applied. Graphs represent arithmetic means ± standard error of the mean (SEM). Differences with P values of <0.05 were considered to be statistically significant. For the purpose of clarity, no stars representing significant differences are depicted in any of the graphs but all possible statistical comparisons and any significant differences are shown in tables that accompany each graph, indicated as: * P <0.05; ** P <0.01; *** P <0.001.
analysis of variance
bone mineral content
bone mineral density
cyclin-dependent kinase inhibitor 1C
cation-independent mannose 6-phosphate receptor
central nervous system
dual energy X-ray absorptiometry
- E11.5 to E17:
5: mouse embryonic days 11.5 to 17.5
fluorescence activated cell sorting
cell cycle growth phase 1
cell cycle growth phase 2
growth factor receptor-bound protein 10
- H & E:
haematoxylin and eosin
insulin-like growth factor
insulin-like growth factor 2
insulin-like growth factor type 2 receptor
mammalian target of rapamycin
optimal cutting temperature
primary mouse embryonic fibroblast
standard error of the mean
cell cycle DNA synthesis phase
white adipose tissue
Raff MC: Size control: the regulation of cell numbers in animal development. Cell. 1996, 86: 173-175. 10.1016/S0092-8674(00)80087-2.
Slack JM: Growth control: action mouse. Curr Biol. 1997, 7: R467-R469. 10.1016/S0960-9822(06)00238-7.
Hafen E, Stocker H: How are the sizes of cells, organs, and bodies controlled?. PLoS Biol. 2003, 1: E6-10.1371/journal.pbio.0000086.
Stanger BZ: Organ size determination and the limits of regulation. Cell Cycle. 2008, 7: 318-324. 10.4161/cc.7.3.5348.
Tumaneng K, Russell RC, Guan KL: Organ size control by Hippo and TOR pathways. Curr Biol. 2012, 22: R368-R379. 10.1016/j.cub.2012.03.003.
Baker J, Liu JP, Robertson EJ, Efstratiadis A: Role of insulin-like growth factors in embryonic and postnatal growth. Cell. 1993, 75: 73-82. 10.1016/0092-8674(93)90680-O.
Burns JL, Hassan AB: Cell survival and proliferation are modified by insulin-like growth factor 2 between days 9 and 10 of mouse gestation. Development. 2001, 128: 3819-3830.
Liu JP, Baker J, Perkins AS, Robertson EJ, Efstratiadis A: Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r). Cell. 1993, 75: 59-72.
Brogiolo W, Stocker H, Ikeya T, Rintelen F, Fernandez R, Hafen E: An evolutionarily conserved function of the Drosophila insulin receptor and insulin-like peptides in growth control. Curr Biol. 2001, 11: 213-221. 10.1016/S0960-9822(01)00068-9.
Barlow DP, Stoger R, Herrmann BG, Saito K, Schweifer N: The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus. Nature. 1991, 349: 84-87. 10.1038/349084a0.
DeChiara TM, Efstratiadis A, Robertson EJ: Parental imprinting of the mouse insulin-like growth factor II gene. Cell. 1991, 64: 849-859. 10.1016/0092-8674(91)90513-X.
Bartolomei MS, Ferguson-Smith AC: Mammalian genomic imprinting. Cold Spring Harb Perspect Biol 2011, 3. doi:10.1101/cshperspect.a002592.,
Kobayashi S, Wagatsuma H, Ono R, Ichikawa H, Yamazaki M, Tashiro H, Aisaka K, Miyoshi N, Kohda T, Ogura A, Ohki M, Kaneko-Ishino T, Ishino F: Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3. Genes Cells. 2000, 5: 1029-1037. 10.1046/j.1365-2443.2000.00390.x.
Bartolomei MS, Zemel S, Tilghman SM: Parental imprinting of the mouse H19 gene. Nature. 1991, 351: 153-155. 10.1038/351153a0.
Ferguson-Smith AC, Sasaki H, Cattanach BM, Surani MA: Parental-origin-specific epigenetic modification of the mouse H19 gene. Nature. 1993, 362: 751-755. 10.1038/362751a0.
Blagitko N, Mergenthaler S, Schulz U, Wollmann HA, Craigen W, Eggermann T, Ropers HH, Kalscheuer VM: Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet. 2000, 9: 1587-1595. 10.1093/hmg/9.11.1587.
Garfield AS, Cowley M, Smith FM, Moorwood K, Stewart-Cox JE, Gilroy K, Baker S, Xia J, Dalley JW, Hurst LD, Wilkinson LS, Isles AR, Ward A: Distinct physiological and behavioural functions for parental alleles of imprinted Grb10. Nature. 2011, 469: 534-538. 10.1038/nature09651.
Willson MF, Burley N: Mate Choice in Plants. 1983, Princeton University Press, Princeton, NJ
Haig D, Westoby M: Parent-specific gene expression and the triploid endosperm. Am Nat. 1989, 134: 147-155. 10.1086/284971.
Gutierrez-Marcos JF, Constancia M, Burton GJ: Maternal to offspring resource allocation in plants and mammals. Placenta. 2012, 33: e3-e10. 10.1016/j.placenta.2012.08.006.
Lau MM, Stewart CE, Liu Z, Bhatt H, Rotwein P, Stewart CL: Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality. Genes Dev. 1994, 8: 2953-2963. 10.1101/gad.8.24.2953.
Wang ZQ, Fung MR, Barlow DP, Wagner EF: Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene. Nature. 1994, 372: 464-467. 10.1038/372464a0.
Ludwig T, Eggenschwiler J, Fisher P, D'Ercole AJ, Davenport ML, Efstratiadis A: Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds. Dev Biol. 1996, 177: 517-535. 10.1006/dbio.1996.0182.
Killian JK, Byrd JC, Jirtle JV, Munday BL, Stoskopf MK, MacDonald RG, Jirtle RL: M6P/IGF2R imprinting evolution in mammals. Mol Cell. 2000, 5: 707-716. 10.1016/S1097-2765(00)80249-X.
Wilkins JF, Haig D: Genomic imprinting of two antagonistic loci. Proc Biol Sci. 2001, 268: 1861-1867. 10.1098/rspb.2001.1651.
Jirtle, RL: Imprinted Genes: by Species http://www.geneimprint.com/site/genes-by-species.,
Smith FM, Garfield AS, Ward A: Regulation of growth and metabolism by imprinted genes. Cytogenet Genome Res. 2006, 113: 279-291. 10.1159/000090843.
Charalambous M, Da Rocha ST, Ferguson-Smith AC: Genomic imprinting, growth control and the allocation of nutritional resources: consequences for postnatal life. Curr Opin Endocrinol Diabetes Obes. 2007, 14: 3-12. 10.1097/MED.0b013e328013daa2.
Wilkinson LS, Davies W, Isles AR: Genomic imprinting effects on brain development and function. Nat Rev Neurosci. 2007, 8: 832-843. 10.1038/nrn2235.
Haig D: Genomic imprinting and kinship: how good is the evidence?. Ann Rev Genet. 2004, 38: 553-585. 10.1146/annurev.genet.37.110801.142741.
Wolf JB, Hager R: A maternal - offspring coadaptation theory for the evolution of genomic imprinting. PLoS Biol. 2006, 4: e380-10.1371/journal.pbio.0040380.
Haig D: Coadaptation and conflict, misconception and muddle, in the evolution of genomic imprinting. Heredity. 2013, 113: 96-103. 10.1038/hdy.2013.97.
Wilkins JF: Genomic imprinting of Grb10: coadaptation or conflict?. PLoS Biol. 2014, 12: e1001800-10.1371/journal.pbio.1001800.
Ball ST, Kelly ML, Robson JE, Turner MD, Harrison J, Jones L, Napper D, Beechey CV, Hough T, Plagge A, Cattanach BM, Cox RD, Peters J: Gene dosage effects at the imprinted Gnas cluster. PLoS One. 2013, 8: e65639-10.1371/journal.pone.0065639.
Varrault A, Gueydan C, Delalbre A, Bellmann A, Houssami S, Aknin C, Severac D, Chotard L, Kahli M, Le Digarcher A, Pavlidis P, Journot L: Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth. Dev Cell. 2006, 11: 711-722. 10.1016/j.devcel.2006.09.003.
Ward A: Beckwith-Wiedemann syndrome and Wilms' tumour. Mol Hum Reprod. 1997, 3: 157-168. 10.1093/molehr/3.2.157.
Grandjean V, Smith J, Schofield PN, Ferguson-Smith AC: Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome. Proc Natl Acad Sci U S A. 2000, 97: 5279-5284. 10.1073/pnas.080409297.
Charalambous M, Smith FM, Bennett WR, Crew TE, Mackenzie F, Ward A: Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2 independent mechanism. Proc Natl Acad Sci. 2003, 100: 8292-8297. 10.1073/pnas.1532175100.
Smith FM, Holt LJ, Garfield AS, Charalambous M, Koumanov F, Perry M, Bazzani R, Sheardown SA, Hegarty BD, Lyons RJ, Cooney GJ, Daly RJ, Ward A: Mice with a disruption of the imprinted Grb10 gene exhibit altered body composition, glucose homeostasis, and insulin signaling during postnatal life. Mol Cell Biol. 2007, 27: 5871-5886. 10.1128/MCB.02087-06.
Charalambous M, Cowley M, Geoghegan F, Smith FM, Radford EJ, Marlow BP, Graham CF, Hurst LD, Ward A: Maternally-inherited Grb10 reduces placental size and efficiency. Dev Biol. 2010, 337: 1-8. 10.1016/j.ydbio.2009.10.011.
Cowley M, Garfield AS, Manon-Simon M, Charalambous M, Clarkson RW, Smalley MJ, Kendrick H, Isles AR, Parry AJ, Carney S, Oakey RJ, Heisler LK, Moorwood K, Wolf JB, Ward A: Developmental programming mediated by complementary roles of imprinted Grb10 in mother and pup. PLoS Biol. 2014, 12: e1001799-10.1371/journal.pbio.1001799.
Wang L, Balas B, Christ-Roberts CY, Kim RY, Ramos FJ, Kikani CK, Li C, Deng C, Reyna S, Musi N, Dong LQ, DeFronzo RA, Liu F: Peripheral disruption of the grb10 gene enhances insulin signaling and sensitivity in vivo. Mol Cell Bio. 2007, 27: 6497-6505. 10.1128/MCB.00679-07.
Holt LJ, Lyons RJ, Ryan AS, Beale SM, Ward A, Cooney GJ, Daly RJ: Dual ablation of Grb10 and Grb14 in mice reveals their combined role in regulation of insulin signaling and glucose homeostasis. Mol Endocrinol. 2009, 23: 1406-1414. 10.1210/me.2008-0386.
Holt LJ, Turner N, Mokbel N, Trefely S, Kanzleiter T, Kaplan W, Ormandy CJ, Daly RJ, Cooney GJ: Grb10 regulates the development of fiber number in skeletal muscle. FASEB J. 2012, 26: 3658-3669. 10.1096/fj.11-199349.
Holt LJ, Siddle K: Grb10 and Grb14: enigmatic regulators of insulin action - and more?. Biochem J. 2005, 388: 393-406. 10.1042/BJ20050216.
Hsu PP, Kang SA, Rameseder J, Zhang Y, Ottina KA, Lim D, Peterson TR, Choi Y, Gray NS, Yaffe MB, Marto JA, Sabatini DM: The mTOR-regulated phosphoproteome reveals a mechanism of mTORC1-mediated inhibition of growth factor signaling. Science. 2011, 332: 1317-1322. 10.1126/science.1199498.
Yu Y, Yoon SO, Poulogiannis G, Yang Q, Ma XM, Villen J, Kubica N, Hoffman GR, Cantley LC, Gygi SP, Blenis J: Phosphoproteomic analysis identifies Grb10 as an mTORC1 substrate that negatively regulates insulin signaling. Science. 2011, 332: 1322-1326. 10.1126/science.1199484.
Liu M, Bai J, He S, Villarreal R, Hu D, Zhang C, Yang X, Liang H, Slaga TJ, Yu Y, Zhou Z, Blenis J, Scherer PE, Dong LQ, Liu F: Grb10 promotes lipolysis and thermogenesis by phosphorylation-dependent feedback inhibition of mTORC1. Cell Metab. 2014, 19: 967-980. 10.1016/j.cmet.2014.03.018.
Moon YS, Smas CM, Lee K, Villena JA, Kim KH, Yun EJ, Sul HS: Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity. Mol Cell Biol. 2002, 22: 5585-5592. 10.1128/MCB.22.15.5585-5592.2002.
Lee K, Villena JA, Moon YS, Kim KH, Lee S, Kang C, Sul HS: Inhibition of adipogenesis and development of glucose intolerance by soluble preadipocyte factor-1 (Pref-1). J Clin Invest. 2003, 111: 453-461. 10.1172/JCI15924.
Villena JA, Choi CS, Wang Y, Kim S, Hwang YJ, Kim YB, Cline G, Shulman GI, Sul HS: Resistance to high-fat diet-induced obesity but exacerbated insulin resistance in mice overexpressing preadipocyte factor-1 (Pref-1): a new model of partial lipodystrophy. Diabetes. 2008, 57: 3258-3266. 10.2337/db07-1739.
Falix FA, Aronson DC, Lamers WH, Gaemers IC: Possible roles of DLK1 in the Notch pathway during development and disease. Biochim Biophys Acta. 1822, 2012: 988-995.
Appelbe OK, Yevtodiyenko A, Muniz-Talavera H, Schmidt JV: Conditional deletions refine the embryonic requirement for Dlk1. Mech Dev. 2013, 130: 143-159. 10.1016/j.mod.2012.09.010.
Mokbel N, Hoffman NJ, Girgis CM, Small L, Turner N, Daly RJ, Cooney GJ, Holt LJ: Grb10 deletion enhances muscle cell proliferation, differentiation and GLUT4 plasma membrane translocation. J Cell Physiol. 2014, 229: 1753-1764. 10.1002/jcp.24628.
Andersen DC, Laborda J, Baladron V, Kassem M, Sheikh SP, Jensen CH: Dual role of delta-like 1 homolog (DLK1) in skeletal muscle development and adult muscle regeneration. Development. 2013, 140: 3743-3753. 10.1242/dev.095810.
Shiura H, Miyoshi N, Konishi A, Wakisaka-Saito N, Suzuki R, Muguruma K, Kohda T, Wakana S, Yokoyama M, Ishino F, Kaneko-Ishino T: Meg1/Grb10 overexpression causes postnatal growth retardation and insulin resistance via negative modulation of the IGF1R and IR cascades. Biochem Biophys Res Comm. 2005, 329: 909-916. 10.1016/j.bbrc.2005.02.047.
Yamamoto Y, Ishino F, Kaneko-Ishino T, Shiura H, Uchio-Yamada K, Matsuda J, Suzuki O, Sato K: Type 2 diabetes mellitus in a non-obese mouse model induced by Meg1/Grb10 overexpression. Exp Anim. 2008, 57: 385-395. 10.1538/expanim.57.385.
Chen L, Qanie D, Jafari A, Taipaleenmaki H, Jensen CH, Saamanen AM, Sanz ML, Laborda J, Abdallah BM, Kassem M: Delta-like 1/fetal antigen-1 (Dlk1/FA1) is a novel regulator of chondrogenic cell differentiation via inhibition of the Akt kinase-dependent pathway. J Biol Chem. 2011, 286: 32140-32149. 10.1074/jbc.M111.230110.
Abdallah BM, Ding M, Jensen CH, Ditzel N, Flyvbjerg A, Jensen TG, Dagnaes-Hansen F, Gasser JA, Kassem M: Dlk1/FA1 is a novel endocrine regulator of bone and fat mass and its serum level is modulated by growth hormone. Endocrinology. 2007, 148: 3111-3121. 10.1210/en.2007-0171.
Abdallah BM, Ditzel N, Mahmood A, Isa A, Traustadottir GA, Schilling AF, Ruiz-Hidalgo MJ, Laborda J, Amling M, Kassem M: DLK1 is a novel regulator of bone mass that mediates estrogen deficiency-induced bone loss in mice. J Bone Min Res. 2011, 26: 1457-1471. 10.1002/jbmr.346.
Cancer Genome Atlas Research Network: Comprehensive molecular characterization of clear cell renal cell carcinoma. Nature. 2013, 499: 43-49. 10.1038/nature12222.
Grignon DJ, Che M: Clear cell renal cell carcinoma. Clin Lab Med. 2005, 25: 305-316. 10.1016/j.cll.2005.01.012.
Haig D, Graham C: Genomic imprinting and the strange case of the insulin-like growth factor II receptor. Cell. 1991, 64: 1045-1046. 10.1016/0092-8674(91)90256-X.
Moore T, Haig D: Genomic imprinting in mammalian development - a parental tug-of-war. Trends Genet. 1991, 7: 45-49. 10.1016/0168-9525(91)90230-N.
Dobbing J, Sands J: Vulnerability of developing brain. IXL: the effect of nutritional growth retardation on the timing of the brain growth-spurt. Biol Neonate. 1971, 19: 363-378. 10.1159/000240430.
Cheng LY, Bailey AP, Leevers SJ, Ragan TJ, Driscoll PC, Gould AP: Anaplastic lymphoma kinase spares organ growth during nutrient restriction in Drosophila. Cell. 2011, 146: 435-447. 10.1016/j.cell.2011.06.040.
Kim SG, Buel GR, Blenis J: Nutrient regulation of the mTOR complex 1 signaling pathway. Mol Cells. 2013, 35: 463-473. 10.1007/s10059-013-0138-2.
Ma XM, Blenis J: Molecular mechanisms of mTOR-mediated translational control. Nat Rev Mol Cell Biol. 2009, 10: 307-318. 10.1038/nrm2672.
Kazi JU, Ronnstrand L: FLT3 signals via the adapter protein Grb10 and overexpression of Grb10 leads to aberrant cell proliferation in acute myeloid leukemia. Mol Oncol. 2013, 7: 402-418. 10.1016/j.molonc.2012.11.003.
Ivanova E, Chen JH, Segonds-Pichon A, Ozanne SE, Kelsey G: DNA methylation at differentially methylated regions of imprinted genes is resistant to developmental programming by maternal nutrition. Epigenetics. 2012, 7: 1200-1210. 10.4161/epi.22141.
Radford EJ, Isganaitis E, Jimenez-Chillaron J, Schroeder J, Molla M, Andrews S, Didier N, Charalambous M, McEwen K, Marazzi G, Sassoon D, Patti ME, Ferguson-Smith AC: An unbiased assessment of the role of imprinted genes in an intergenerational model of developmental programming. PLoS Genet. 2012, 8: e1002605-10.1371/journal.pgen.1002605.
Smas CM, Sul HS: Pref-1, a protein containing EGF-like repeats, inhibits adipocyte differentiation. Cell. 1993, 73: 725-734. 10.1016/0092-8674(93)90252-L.
Smas CM, Chen L, Sul HS: Cleavage of membrane-associated pref-1 generates a soluble inhibitor of adipocyte differentiation. Mol Cell Biol. 1997, 17: 977-988.
Garces C, Ruiz-Hidalgo MJ, Bonvini E, Goldstein J, Laborda J: Adipocyte differentiation is modulated by secreted delta-like (dlk) variants and requires the expression of membrane-associated dlk. Differentiation. 1999, 64: 103-114. 10.1007/s002580050265.
Ruiz-Hidalgo MJ, Gubina E, Tull L, Baladron V, Laborda J: dlk modulates mitogen-activated protein kinase signaling to allow or prevent differentiation. Exp Cell Res. 2002, 274: 178-188. 10.1006/excr.2001.5464.
Zhang H, Noohr J, Jensen CH, Petersen RK, Bachmann E, Teisner B, Larsen LK, Mandrup S, Kristiansen K: Insulin-like growth factor-1/insulin bypasses Pref-1/FA1-mediated inhibition of adipocyte differentiation. J Biol Chem. 2003, 278: 20906-20914. 10.1074/jbc.M300022200.
Kim KA, Kim JH, Wang Y, Sul HS: Pref-1 (preadipocyte factor 1) activates the MEK/extracellular signal-regulated kinase pathway to inhibit adipocyte differentiation. Mol Cell Biol. 2007, 27: 2294-2308. 10.1128/MCB.02207-06.
Wang Y, Zhao L, Smas C, Sul HS: Pref-1 interacts with fibronectin to inhibit adipocyte differentiation. Mol Cell Biol. 2010, 30: 3480-3492. 10.1128/MCB.00057-10.
Raghunandan R, Ruiz-Hidalgo M, Jia Y, Ettinger R, Rudikoff E, Riggins P, Farnsworth R, Tesfaye A, Laborda J, Bauer SR: Dlk1 influences differentiation and function of B lymphocytes. Stem Cells Dev. 2008, 17: 495-507. 10.1089/scd.2007.0102.
Bennett WR, Crew TE, Slack JM, Ward A: Structural-proliferative units and organ growth: effects of insulin-like growth factor 2 on growth of colon and skin. Development. 2003, 130: 1079-1088. 10.1242/dev.00333.
Bancroft JD, Gamble M: Theory and Practice of Histological Techniques. 2002, Churchill Livingstone, London, UK, 5
McLeod MJ: Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S. Teratology. 1980, 22: 299-301. 10.1002/tera.1420220306.
White CR, Seymour RS: Mammalian basal metabolic rate is proportional to body mass2/3. Proc Natl Acad Sci U S A. 2003, 100: 4046-4049. 10.1073/pnas.0436428100.
Lahiri D, Dutton JR, Duarte A, Moorwood K, Graham CF, Ward A: Nephropathy and defective spermatogenesis in mice transgenic for a single isoform of the Wilms' tumour suppressor protein (WT1-KTS) together with one disrupted Wt1 allele. Mol Reprod Dev. 2006, 74: 300-311. 10.1002/mrd.20491.
Garfield AS: Derivation of primary mouse embryonic fibroblast (PMEF) cultures. Methods Mol Biol. 2010, 633: 19-27. 10.1007/978-1-59745-019-5_2.
We thank Mark Perry, Adrian Rogers and Iryna Withington for technical assistance, and Anne Ferguson-Smith and Marika Charalambous for discussions during the course of the work. We are grateful for funding for the work from the Medical Research Council UK (studentship to ASG and research grant award to AW) and the University of Bath (studentships to MM-S and MC; post-doctoral funds to KM).
The authors declare that they have no competing interests.
MM-S and AW designed the experiments. MM-S, MC, ASG, KM and AW performed the experiments. SRB supplied the Dlk1 knockout mouse model. MM-S and AW wrote the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Figure S1.: Analyses of fetal and placental wet weights at E12.5 and E17.5A). A) At E12.5 both Grb10 m/+ and Grb10 m/+/Dlk1 +/p fetuses, but not placentae, were significantly heavier than wild type and Dlk1 +/p littermates. B) At E17.5 Grb10 m/+ and Grb10 m/+/Dlk1 +/p fetuses were significantly heavier than wild type and Dlk1 +/p littermates, and in addition Grb10 m/+ and Grb10 m/+/Dlk1 +/p placentae were heavier than Dlk1 +/p placentae. C) Table summarising results of statistical analysis in A and B. All values represent means ± SEM, one way ANOVA with Tukey’s post-hoc analysis. For E12.5 WT n = 23, Dlk1 +/p n = 13, Grb10 m/+ n = 13, Grb10 m/+/Dlk1 +/p n = 16; for E17.5 WT n = 4, Dlk1 +/p n = 8, Grb10 m/+ n = 6, Grb10 m/+/Dlk1 +/p n = 8; * P <0.05; ** P <0.01; *** P <0.001. (PDF 256 KB)
Additional file 2: Figure S2.: Cell size analysis by FACS of E14.5 PMEFs and disaggregated E11.5 fetuses. A) Cultured E14.5-derived PMEFs, at passage 3, were stained with propidium iodide and cell size determined by FACS for 100,000 cells per sample. Cells were allocated to one of four arbitrary gates (0 to 25 k, >25 to 50 k, >50 to 75 k, >75 to 100 k) to allow statistical comparison of cell size distribution. B) Table summarising results of statistical analysis of data in A. All values represent means ± SEM, one way ANOVA with Tukey’s post-hoc analysis. WT n = 7, Dlk1 +/p n = 7, Grb10 m/+ n = 7, Grb10 m/+/Dlk1 +/p n = 6. No significant differences were observed between cells of any of the four genotypes. C) Cells derived directly from wild type, Dlk1 +/p, Grb10 m/+ and Grb10 m/+/Dlk1 +/p E11.5 fetuses were stained with propidium iodide and cell size determined by FACS for 100,000 cells per sample. Cells were allocated to one of four arbitrary gates (0 to 25 k, >25 to 50 k, >50 to 75 k, >75 to 100 k) to allow statistical comparison of cell size distribution. D) Table summarising results of statistical analysis of data in C. All values represent means ± SEM, one way ANOVA with Tukey’s post-hoc analysis. WT n = 7, Dlk1 +/p n = 7, Grb10 m/+ n = 6, Grb10 m/+/Dlk1 +/p n = 8. No significant differences were observed between cells of any of the four genotypes. (PDF 301 KB)
Additional file 3: Figure S3.: Whole body and organ wet weight analysis of wild type, Dlk1 +/p, Grb10 m/+ and Grb10 m/+/Dlk1 +/p neonates. A) Grb10 m/+ and Grb10 m/+/Dlk1 +/p animals showed whole body overgrowth, whereas Dlk1 +/p mice were significantly growth retarded when compared to wild type and Dlk1 +/p mice. Note, this graph is the same as that shown in Figure 4A, reproduced here for convenience. B) Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice had overgrown brains when compared to wild type and Dlk1 +/p animals. C) Significant enlargement of the livers was noted in Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice compared to wild type and Dlk1 +/p animals. D) Significant overgrowth of kidneys was seen in Grb10 m/+/Dlk1 +/p mice compared to Dlk1 +/p. E) Significant enlargement of the lungs was observed in Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice compared to wild type and Dlk1 +/p animals. F) Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice exhibited significantly enlarged hearts compared to wild type and Dlk1 +/p animals. G) Table summarising results of statistical analysis. All values represent means ± SEM, analysed using one way ANOVA with Tukey’s post-hoc analysis. WT n = 19, Dlk1 +/p n = 36, Grb10 m/+ n = 23, Grb10 m/+/Dlk1 +/p n = 22; * p < 0.05; *** P <0.001. (PDF 306 KB)
Additional file 4: Figure S4.: Histology of neonatal and adult livers stained with H & E. A) Histological examination of neonatal livers stained with H & E revealed that Dlk1 +/p sections were indistinguishable from wild type, but Grb10 m/+ and Grb10 m/+/Dlk1 +/p livers showed the presence of abundant white, round spaces (WT n = 5, Dlk1 +/p n = 6, Grb10 m/+ n = 4 and Grb10 m/+/Dlk1 +/p n = 5). B) There were no differences in wild type, Grb10 m/+ and Grb10 m/+/Dlk1 +/p adult livers (from males at three months of age); however, the presence of large and abundant white, round spaces was noted in Dlk1 +/p livers (n = 5 for each genotype). Presented images (in A and B) show representative sections for each of the analysed genotypes. (PNG 5 MB)
Additional file 5: Figure S5.: DXA analysis of adult wild type, Grb10 m/+, Dlk1 +/p and Grb10 m/+/Dlk1 +/p female mice. Carcasses of female animals three- to nine-months-old were analysed by DXA. A) No differences were found in bone mineral density (BMD). B) Bone mineral content was significantly reduced in Dlk1 +/p mice in comparison to wild type. C) Total lean tissue mass was significantly elevated in Grb10 m/+ animals when compared to Dlk1 +/p D) No changes were seen in total fat tissue content. E) Lean mass as a percentage of total body mass was significantly increased in Grb10 m/+ mice in comparison to Dlk1 +/p mice. F) Fat mass as a percentage of total body mass was significantly reduced in Grb10 m/+ mice when compared to Dlk1 +/p. G) Table summarising results of statistical analysis. All values represent means ± SEM and have been subject to one way ANOVA with post hoc Tukey’s analysis. WT n = 13, Dlk1 +/p n = 12, Grb10 m/+ n = 12 and Grb10 m/+/Dlk1 +/p n = 12; * P <0.05; ** P <0.01. (PDF 312 KB)
Additional file 6: Figure S6.: Analysis of white adipose tissue sections from three-month-old mice. A) H & E stained sections of white adipose tissue. No obvious differences were noted between any of the analysed genotypes. Images are representative sections viewed at 100x magnification for each of the analysed genotypes, WT n = 6, Dlk1 +/p =5, Grb10 m/+ n = 6 and Grb10 m/+/Dlk1 +/p n = 6. B-E) Morphometric analysis was carried out on images captured at 200x magnification, used to analyse adipocyte cell numbers (B) and cell areas (C), as well as mean (D) and maximum cell widths (E). F) Table summarising results of statistical analysis. All values represent means ± SEM and have been subject to one way ANOVA with post hoc Tukey’s analysis. WT n = 5, Dlk1 +/p n = 5, Grb10 m/+ n = 5 and Grb10 m/+/Dlk1 +/p n = 5. No significant differences (ns; P >0.05) were found for any of the analysed parameters. (PNG 2 MB)
Additional file 7: Figure S7.: Analysis of food consumption. Food intake was monitored over a period of two weeks. Total consumption is shown for males (A) and females (B) and food consumption rates have been calculated as food consumed per gram of animal body weight per day to the power of 2/3 (to take account of basal metabolic rate as a function of body mass ), again for males (C) and females (D). E) Table summarising results of statistical analysis. All values represent means ± SEM and have been subject to one way ANOVA with post hoc Tukey’s analysis. Males: WT n = 14, Dlk1 +/p =12, Grb10 m/+ n = 12 and Grb10 m/+/Dlk1 +/p n = 13; females: WT n = 13, Dlk1 +/p n = 12, Grb10 m/+ n = 12 and Grb10 m/+/Dlk1 +/p n = 12. No significant differences (ns, P >0.05) were found in either the total amount of food consumed by males and females or in the rate of food consumption. (PDF 240 KB)
Additional file 8: Figure S8.: Skeletal analyses. A) In sections of neonatal wild type, Grb10 m/+, Dlk1 +/p and Grb10 m/+/Dlk1 +/p femurs LacZ (blue) staining was detected in Grb10 m/+ and Grb10 m/+/Dlk1 +/p mice, specifically in growth plates and muscle tissue adjacent to the long bones, but not in wild type and Dlk1 +/p mice, which do not carry an integrated LacZ reporter gene. The images show the distal growth plate (GP) of the femur, with associated muscle (M) and in some cases the knee joint and adjacent growth plate of the tibia. Presented images (400x magnification) show representative sections for each of the analysed genotypes. WT n = 4, Dlk1 +/p n = 4, Grb10 m/+ n = 6 and Grb10 m/+/Dlk1 +/p n = 3. B) Alcian Blue (cartilage) and Alizarin Red (bone) staining of skeletons from mice at two weeks of age revealed no obvious differences, including in the ribs and sternum previously reported to be malformed in Dlk1 knockout mice (Moon et al. ). (PNG 4 MB)
Additional file 9: Figure S9.: Histology of adult kidney. In kidney sections from three-month-old males LacZ (blue) staining was observed in proximal tubules (characterised by distinctive brush border cells; (BB) of Grb10 m/+ and Grb10 m/+/Dlk1 +/p, but not WT or Dlk1 +/p, mice. Presented images show representative sections for each of the analysed genotypes, counterstained with nuclear fast red (200x magnification). WT n = 4, Dlk1 +/p n = 3, Grb10 m/+ n = 3 and Grb10 m/+/Dlk1 +/p n = 3. (PNG 3 MB)
Authors’ original submitted files for images
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