Fig. 5From: Lineage-specific, fast-evolving GATA-like gene regulates zygotic gene activation to promote endoderm specification and pattern formation in the Theridiidae spiderfuchi transcript expression in specific cells on the embryonic and abembryonic sides of early embryos. A–H Chromogenic WISH of wild-type embryos at indicated stages using fuchi probes (left), counterstained for DNA (right). A, B Opposite sides of the same embryo. Arrowhead indicates the signal. C–F Lateral view. The forming/formed germ disc (gd) is up. Arrowheads denote cells expressing fuchi at or near the germ-disc rim. G, H Forming germ band (gb) with expanding extraembryonic region (ex). Asterisks mark the embryonic pole, closed blastopore, or posterior pole. I–O Reconstruction of confocal stacks showing wild-type embryos fluorescently stained for fuchi (green) and DNA (blue) at 15 (I, J), 21 (K), 25 (L, M), 32 (N), and 38 (O) h AEL. Asterisks mark the embryonic pole or closed blastopore. I, J The same embryo from different directions. I’–M’, N1, N2, O2 High magnification of the boxed areas in I–O. Cell–cell junctions visualized by β-catenin staining are traced in I’–M’, and N2. I”–M”, N2’, O2’ Optical sections corresponding to the rectangular regions in I’–M’, N2, and O2. Arrowheads indicate fuchi-expressing cells that appear to be internalizing or internalized. N1’, O1 Optical sections corresponding to the lines in N and O. β-Catenin signals (red) are overlaid in I”, L”, N1’, and O1. β-Catenin concentrations mark the cumulus (cm). Fat arrows indicate fuchi expression in the future extraembryonic region. P, P’, Q, Q’ Simultaneous detection of fuchi (green) and Pt-hh (red) transcripts and DNA (blue) at or near the germ-disc rim at early (P, P’) and late (Q, Q’) stage 5. Arrowheads indicate cells expressing both fuchi and Pt-hh before internalization and cells expressing only fuchi after internalization. Em, embryonic side; Ab, abembryonic side. Scale bars, 100 µm in A, I–O; 20 µm in other panelsBack to article page