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Targeted mutagenesis of the Hira gene results in gastrulation defects and patterning abnormalities of mesoendodermal derivatives prior to early embryonic lethality.

TitleTargeted mutagenesis of the Hira gene results in gastrulation defects and patterning abnormalities of mesoendodermal derivatives prior to early embryonic lethality.
Publication TypeJournal Article
Year of Publication2002
AuthorsRoberts C, Sutherland HF, Farmer H, Kimber W, Halford S, Carey A, Brickman JM, Wynshaw-Boris A, Scambler PJ
JournalMol Cell Biol
Volume22
Issue7
Pagination2318-28
Date Published2002 Apr
ISSN0270-7306
KeywordsAnimals, Blotting, Western, Body Patterning, Cell Cycle Proteins, Congenital Abnormalities, Embryo Loss, Embryonic and Fetal Development, Gastrula, Gene Deletion, Genes, Essential, Histone Chaperones, Homozygote, Immunohistochemistry, In Situ Hybridization, Mesoderm, Mice, Mutagenesis, Site-Directed, Nervous System, Nuclear Proteins, Phenotype, Reverse Transcriptase Polymerase Chain Reaction, RNA, Messenger, Transcription Factors
Abstract

The Hira gene encodes a nuclear WD40 domain protein homologous to the yeast transcriptional corepressors Hir1p and Hir2p. Using targeted mutagenesis we demonstrate that Hira is essential for murine embryogenesis. Analysis of inbred 129Sv embryos carrying the null mutation revealed an initial requirement during gastrulation, with many mutant embryos having a distorted primitive streak. Mutant embryos recovered at later stages have a range of malformations with axial and paraxial mesendoderm being particularly affected, a finding consistent with the disruption of gastrulation seen earlier in development. This phenotype could be partially rescued by a CD1 genetic background, although the homozygous mutation was always lethal by embryonic day 11, with death probably resulting from abnormal placentation and failure of cardiac morphogenesis.

Alternate JournalMol. Cell. Biol.
PubMed ID11884616
PubMed Central IDPMC133693