共 36 条
Asymmetric Localization of Cdx2 mRNA during the First Cell-Fate Decision in Early Mouse Development
被引:56
|作者:
Skamagki, Maria
[1
]
Wicher, Krzysztof B.
[1
]
Jedrusik, Agnieszka
[1
]
Ganguly, Sujoy
[2
]
Zernicka-Goetz, Magdalena
[1
]
机构:
[1] Univ Cambridge, Gurdon Inst, Cambridge CB2 1QN, England
[2] Univ Cambridge, Dept Appl Math & Theoret Phys, Cambridge CB3 0WA, England
来源:
基金:
英国惠康基金;
关键词:
TROPHECTODERM LINEAGE;
TRANSCRIPTION FACTOR;
EMBRYO;
SPECIFICATION;
DROSOPHILA;
BLASTOCYST;
TRANSPORT;
TEAD4;
MASS;
DIFFERENTIATION;
D O I:
10.1016/j.celrep.2013.01.006
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
A longstanding question in mammalian development is whether the divisions that segregate pluripotent progenitor cells for the future embryo from cells that differentiate into extraembryonic structures are asymmetric in cell-fate instructions. The transcription factor Cdx2 plays a key role in the first cell-fate decision. Here, using live-embryo imaging, we show that localization of Cdx2 transcripts becomes asymmetric during development, preceding cell lineage segregation. Cdx2 transcripts preferentially localize apically at the late eight-cell stage and become inherited asymmetrically during divisions that set apart pluripotent and differentiating cells. Asymmetric localization depends on a cis element within the coding region of Cdx2 and requires cell polarization as well as intact microtubule and actin cytoskeletons. Failure to enrich Cdx2 transcripts apically results in a significant decrease in the number of pluripotent cells. We discuss how the asymmetric localization and segregation of Cdx2 transcripts could contribute to multiple mechanisms that establish different cell fates in the mouse embryo.
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页码:442 / 457
页数:16
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