Mixl1 is required for axial mesendoderm morphogenesis and patterning in the murine embryo
Details
Publication Year 2002-08-01,Volume 129,Issue #15,Page 3597-3608
Journal Title
DEVELOPMENT
Publication Type
Journal Article
Abstract
In Xenopus, the Mix/Bix family of homeobox genes has been implicated in mesendoderm development. Mixl1 is the only known murine member of this family. To examine the role of Mixl1 in murine embryogenesis, we used gene targeting to create mice bearing a null mutation of Mixl1. Homozygous Mixl1 mutant embryos can be distinguished from their littermates by a marked thickening of the primitive streak. By the early somite stage, embryonic development is arrested, with the formation of abnormal head folds, foreshortened body axis, absence of heart tube and gut, deficient paraxial mesoderm, and an enlarged midline tissue mass that replaces the notochord. Development of extra-embryonic structures is generally normal except that the allantois is often disproportionately large for the size of the mutant embryo. In chimeras, Mixl1(-/-) mutant cells can contribute to all embryonic structures, with the exception of the hindgut, suggesting that Mixl1 activity is most crucial for endodermal differentiation. Mixl1 is therefore required for the morphogenesis of axial mesoderm, the heart and the gut during embryogenesis.
Publisher
COMPANY OF BIOLOGISTS LTD
Keywords
GERM LAYER FORMATION; XENOPUS GENE MIX.1; ENDODERM FORMATION; HOMEOBOX GENE; MOUSE EMBRYO; PRIMITIVE STREAK; DEFINITIVE ENDODERM; HOMEODOMAIN PROTEINS; MESODERM INDUCTION; NODAL EXPRESSION
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Creation Date: 2002-08-01 12:00:00
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