Maternal Cdx2 is dispensable for mouse development

被引:48
作者
Blij, Stephanie [1 ]
Frum, Tristan [1 ]
Akyol, Aytekin [2 ,3 ,4 ,5 ]
Fearon, Eric [2 ,3 ,4 ,5 ]
Ralston, Amy [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Mol Cell & Dev Biol, Santa Cruz, CA 95064 USA
[2] Univ Michigan, Sch Med, Dept Internal Med, Div Mol Med & Genet, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Human Genet, Div Mol Med & Genet, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Pathol, Div Mol Med & Genet, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Sch Med, Ctr Canc, Ann Arbor, MI 48109 USA
来源
DEVELOPMENT | 2012年 / 139卷 / 21期
基金
美国国家卫生研究院;
关键词
Blastocyst; Maternal-effect gene; Trophectoderm; Caudal; CRE RECOMBINASE; PROVIDED CDX2; CELL FATE; EMBRYO; EXPRESSION; TROPHECTODERM; BLASTOCYST; MICE; SPECIFICATION; DOWNSTREAM;
D O I
10.1242/dev.086025
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In many invertebrate and vertebrate species, cell fates are assigned through the cellular inheritance of differentially localized maternal determinants. Whether mammalian embryogenesis is also regulated by deterministic mechanisms is highly controversial. The caudal domain transcription factor CDX2 has been reported to act as a maternal determinant regulating cell fate decisions in mouse development. However, this finding is contentious because of reports that maternal Cdx2 is not essential for development. Notably, all of the previously published studies of maternal Cdx2 relied on injected RNA interference constructs, which could introduce experimental variation. Only deletion of the maternal gene can unambiguously resolve its requirement in mouse development. Here, we genetically ablated maternal Cdx2 using a Cre/lox strategy, and we definitively establish that maternal Cdx2 is not essential for mouse development.
引用
收藏
页码:3969 / 3972
页数:4
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