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The hypoblast (visceral endoderm): an evo-devo perspective
Author(s) -
Claudio D. Stern,
Karen M. Downs
Publication year - 2012
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.070730
Subject(s) - epiblast , biology , primitive streak , gastrulation , endoderm , forebrain , microbiology and biotechnology , mesoderm , neural plate , homeobox , blastula , embryonic stem cell , anatomy , germ layer , embryogenesis , brachyury , embryo , genetics , neuroscience , induced pluripotent stem cell , central nervous system , gene expression , gene
When amniotes appeared during evolution, embryos freed themselves from intracellular nutrition; development slowed, the mid-blastula transition was lost and maternal components became less important for polarity. Extra-embryonic tissues emerged to provide nutrition and other innovations. One such tissue, the hypoblast (visceral endoderm in mouse), acquired a role in fixing the body plan: it controls epiblast cell movements leading to primitive streak formation, generating bilateral symmetry. It also transiently induces expression of pre-neural markers in the epiblast, which also contributes to delay streak formation. After gastrulation, the hypoblast might protect prospective forebrain cells from caudalizing signals. These functions separate mesendodermal and neuroectodermal domains by protecting cells against being caught up in the movements of gastrulation.

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