Butterfly eyespot serial homology: enter the Hox genes
BMC Biology volume 9, Article number: 26 (2011)
Hox genes modify serial homology patterns in many organisms, exemplified in vertebrates by modification of the axial skeleton and in arthropods by diversification of the body segments. Butterfly wing eyespots also appear in a serial homologous pattern that, in certain species, is subject to local modification. A paper in EvoDevo reports the Hox gene Antp is the earliest known gene to have eyespot-specific expression; however, not all Lepidoptera express Antp in eyespots, suggesting some developmental flexibility.
See research article: http://www.evodevojournal.com/content/2/1/9
A common occurrence during development is the formation of repeated homologous structures. During evolution, some of the elements of such serial homology groups may become specialized to perform specific functions, leading to the morphological diversification of the serial homology elements. The best-studied homology series in animals are the body segments, which initially arise as a series of identical subdivisions and then undergo diversification to give rise to segment-specific structures, such as segments with or without legs in the arthropods or vertebrae with or without ribs in vertebrates. This morphological diversification is regulated by Hox genes. A recent paper published in EvoDevo has identified the Antennapedia (Antp) Hox gene as the earliest known gene to have eyespot-specific expression . However, Antp is not expressed in the eyespots of all Lepidoptera species, uncovering the existence of developmental flexibility in eyespot morphogenesis during evolution.
The pigmented concentric rings observed in eyespots are induced during development by the group of cells located in its centre, called the focus. Nijhout, in early work, discovered that if the focus of the pupal wing is transplanted to another area of the wing, it can induce the formation of an ectopic eyespot in the surrounding cells . Moreover, cauterization of the focus inhibits eyespot formation. These experiments suggested a model (Figure 1A) wherein the focus secretes a signalling molecule, which acts as a morphogen present at decreasing concentration as it spreads away from the source. The cells surrounding the focus would perceive different amounts of morphogen and, depending on the concentration they detect, would activate one or another pigment, giving rise to the pattern of concentric colour rings.
The morphogen model of eyespot development
The morphogen model has received strong backing over the years since the discovery that several signalling molecules and transcription factors known for their function in controlling Drosophila development, in which the morphogen model is well established, are expressed in the focus and in circular patterns in the eyespot of several butterfly species [3–5]. For example, in the Squinting Bush Brown butterfly Bicyclus anynana, an important model organism for the study of developmental plasticity and the formation of wing patterning, the focus expresses Wingless (Wg) and phospho-SMAD protein, an indicator of TGFβ signalling activation, suggesting that the focus secretes at least two well-characterized Drosophila morphogens . In the Peacock butterfly Precis coenia (aka. Junonia coenia), there is evidence that the focus expresses high levels of the signalling protein Hedgehog (Hh), which activate its receptor, Patched (Ptc), and the signal transducer Cubitus interruptus (Ci) . Moreover, the Notch (N) receptor is upregulated in the focus of many different butterfly species [1, 5]. Besides this richness of signalling pathways, several developmental transcription factors are specifically upregulated in the eyespot, including the Engrailed (En) and the Distalless (Dll) homeodomain proteins, as well as the Spalt (Sal) zinc finger protein .
Temporal regulation of eyespot development
Temporal analysis of gene expression shows that the specification of the eyespot occurs at the last larval stage, when En, Dll, Sal and N become activated in the focus. The recruitment to the eyespot of these developmental genes that are normally required in insects to make the legs and the wings represents a butterfly innovation in the evolution of this novel trait. Later, at the pupal stage, Wg and phospho-SMAD are detected in the focus, followed by the secondary activation of En, Sal and Dll in eyespot cells surrounding the focus . This gives an idea of an early specification of the focus, followed by the activation of a number of ligands that induce around the focus the concentric activation of the transcription factors regulating pigmentation (Figure 1A). Interestingly, in some species, there are many more foci specified at the larval stage than eyespots will later develop, indicating that modulation of the eyespot development cascade at pupal stages may be responsible for the modification of the serial homology elements.
Saenko and collaborators  have now discovered that Antp is the earliest transcription factor activated in foci known to date. Antp expression appears in all foci primordia, including those that will not contribute to an eyespot in the adult. This indicates that Antp function may be important for early eyespot specification, but it is unlikely to be responsible for regulating the departure from the basal serial homology. Thus, in butterflies, Antp function has been co-opted to the eyespots, where its function, still to be identified, is unlikely to be the modification of serial homologous structures for which Hox genes are well known.
Studies of gene function in eyespot support the morphogen model
Although the expression of Antp and other developmental genes during eyespot formation is an exciting finding, the field is struggling to obtain functional information about the role each of these genes plays in eyespot formation. This is due to both the sparsity of eyespot mutant variants and the inefficient penetration of RNAi in the butterfly epidermis, where the eyespots form . Current research is aimed at generating new constructs that will help to assay ectopic gene expression and improve RNAi-induced loss of function in butterflies and other organisms .
Despite all these difficulties, genetic analysis is slowly confirming some predictions of the morphogen model. Recently, Saenko and collaborators  studied three allelic dominant spontaneous mutations (Bigeye, Frodo and Spread) in the BFS gene of Bicyclus anynana. When heterozygous, these alleles affect eyespot size and colour, and, when homozygous, some allele combinations are lethal, giving rise to embryos with a "segment polarity" phenotype similar to that caused in Drosophila by mutations in en, hh or wg. Homozygous BFS embryos have normal wg and en early expression in segmental stripes, but at later embryonic stages, wg and en are expressed in neighbouring cells, forming wider segmental bands. These experiments indicate that BFS controls, directly or indirectly, the maintenance of Wg and Hh signalling in the embryo and probably in the eyespots. Although the BFS gene product has not yet been characterized, it is located in a genomic region where there are no conserved genes, suggesting that BFS may represent a novel Lepidoptera segment polarity regulator.
Gene networks in eyespot development
An interesting question is to what extent eyespots are patterned in all butterfly species using the same gene networks. Research in many species has highlighted that eyespots in Nymphalid butterflies and Saturnid moths express En, Sal and Dll, indicating similarities in the way all eyespots are formed. However, recent research shows that there are also many differences. For example, while expression of En and Ci is preceded in Junonia coenia by increased levels of hh and ptc in the foci , in B. anynana, hh and ptc are not upregulated, suggesting that En and Ci are activated differently in the two species. Similarly, while Antp is expressed in the foci of B. anynana and five related species, it is not detected in the foci of Junonia coenia and two related species . These observations are very intriguing. If, as proposed, eyespots are a novel morphological trait that originated once and was retained and modified in different butterfly species, we may be observing that the developmental gene network that originally gave rise to the eyespot has been modulated differently in various species without modifying the final outcome. This is similar to the different ways in which short and long germ-band insects have modified the early gene network controlling segmentation. Although at the phylotypic stage all insect embryos are morphologically similar, this stage is reached in different ways: in long germ-band insects such as Drosophila, the embryo is segmented simultaneously, while in short germ-band insects such as Tribolium (the flour beetle), segmentation happens by adding segments sequentially.
How can these developmental differences occur, and where is the developmental plasticity coming from? In the case of the butterfly eyespots, there may be some clues to the possible source of plasticity. It has been observed that injury in the pupal wing induces the formation of ectopic eyespots . At late pupal stages, wound-induced eyespots (Figure 1B) express the same patterning genes as those expressed during normal eyespot development , showing that the late eyespot gene network can be deployed correctly using different initial conditions. It may be this kind of flexibility that evolution is exploring to generate the observed developmental gene network diversity.
Butterfly eyespot development likely conforms to a morphogen model; however, the initiating factors and some downstream components of these genetic pathways may vary among species. Understanding the diversity of eyespot development may shed light on the plasticity of developmental pathways within and between species.
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JC-GH is funded by research grants of the Spanish MICINN, the Junta de Andalucía, the Consolider Program and the European Regional Development Fund.
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Hombría, J.CG. Butterfly eyespot serial homology: enter the Hox genes. BMC Biol 9, 26 (2011). https://doi.org/10.1186/1741-7007-9-26