Complementary functions of otx2 and cripto in initial patterning of mouse epiblast

68Citations
Citations of this article
64Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The development of the mammalian antero-posterior (A-P) axis is proposed to be established by distinct anterior and posterior signaling centers, anterior visceral endoderm and primitive streak, respectively. Knock-out studies in mice have shown that Otx2 and Cripto have crucial roles in the generation and/or functions of these anterior and posterior centers, respectively. In both Otx2 and Cripto single mutants, the initial formation of the A-P axis takes place in a proximal-distal (P-D) orientation, but subsequent axis rotation fails to occur. To examine the developmental consequences of the lack of these two genes, we have analyzed the Otx2−/−;Cripto−/− double homozygous mutant phenotype. In the double mutants, the expression of the A-P axis markers Cer-1, Lim1, and Wnt3 was not induced, while expression of Fgf8 and T was expanded throughout the epiblast, indicating that the double mutants could not form the A-P axis even in its initial P-D orientation. In addition, the double mutants displayed defects in differentiation of the visceral endoderm overlying the epiblast, as well as in the extraembryonic ectoderm. Furthermore, differentiation of neuroectoderm was accelerated as judged by the reduction of Oct4 expression and emergence of Sox1 and Gbx2 expression in the double mutant epiblast. The resulting ectoderm only displayed characteristics of anterior hindbrain, implicating it as a ground state in the mammalian body plan. Our results indicate that complementary functions of Otx2 and Cripto are essential for initial patterning of the A-P axis in the mouse embryo. © 2001 Academic Press.

Cite

CITATION STYLE

APA

Kimura, C., Shen, M. M., Takeda, N., Aizawa, S., & Matsuo, I. (2001). Complementary functions of otx2 and cripto in initial patterning of mouse epiblast. Developmental Biology, 235(1), 12–32. https://doi.org/10.1006/dbio.2001.0289

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free