Abstract

BackgroundChick definitive endoderm is an important source of signals that pattern the early embryo forming a central structure around which the body plan is constructed. Although the origin of definitive endoderm has been mapped in the chick, arising principally from rostral streak at elongating streak stages, it is not known when this layer first becomes fully committed to its germ layer fate, an important issue to resolve in light of its critical role in subsequent patterning of the early embryo.ResultsThrough gene expression screening of chick gastrula, we identified molecular markers of definitive endoderm restricted to rostral (Sox17) and caudal (Gata5/6) regions, suggesting that at least two subpopulations of definitive endodermal cells exist during ingression. We show (1) that presumptive mesoderm cells migrate to the middle layer and remain mesenchymal when transplanted to rostral primitive streak, and prospective endoderm cells enter the lower layer and become epithelial when transplanted to caudal primitive streak; and (2) that presumptive endoderm cells and mesoderm cells lose normal gene expression (Sox17 and Wnt8c, respectively) when transplanted outside of their normal position of origin. Moreover, when rostral or caudal primitive streak segments are transplanted into rostral blastoderm isolates (RBIs), both types of transplants express Sox17 4–6 hours later–consistent with their new position, regardless of their presumptive germ layer origin–and prospective mesoderm transplants, which normally express Wnt8c, turn off expression, suggesting that signals within the rostral blastoderm induce endoderm gene expression, and repress mesoderm gene expression, during gastrulation.ConclusionOur results demonstrate that germ layer identity is fixed at the time populations of endoderm and mesoderm cells ingress through the primitive streak, whereas their gene expression patterns remain labile. In addition, our results show that inductive and repressive signals are present, and that these signals regulate gene expression of both ingressed endoderm and mesoderm cells. Thus, gastrula cells display elements of both pre-patterning and plasticity, with endoderm the first germ layer becoming committed to its fate during early gastrulation stages.

Highlights

  • Chick definitive endoderm is an important source of signals that pattern the early embryo forming a central structure around which the body plan is constructed

  • We examined the chick orthologues of a number of potential definitive endoderm markers using in situ hybridization (ISH) to determine their expression patterns (i.e., Gata4, 5, 6, Sox17, Foxa2/Hnf3beta, Hnf4alpha, Mix, Edd, MafA)

  • Sox17 gene expression Definitive endoderm is marked by the expression of the Sry-related HMG box gene, Sox17, in Xenopus, mouse and zebrafish

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Summary

Introduction

Chick definitive endoderm is an important source of signals that pattern the early embryo forming a central structure around which the body plan is constructed. The origin of definitive endoderm has been mapped in the chick, arising principally from rostral streak at elongating streak stages, it is not known when this layer first becomes fully committed to its germ layer fate, an important issue to resolve in light of its critical role in subsequent patterning of the early embryo. Formation of endoderm has been studied in a number of animal models, for example, in Xenopus, maternally derived VegT acts via Nodal signaling upstream of Mix, Gata and Xsox in specification of definitive endoderm. A recent microarray study in Xenopus has revealed some 300 endoderm-expressed genes, with identification of a number of novel Nodal, Mixer and Sox proteins [12]. With less than 10% of the endoderm transcriptome being regulated as predicted, the linear model of endoderm development is under renewed scrutiny

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