Downstream of Identity Genes: Muscle-Type-Specific Regulation of the Fusion Process

被引:43
作者
Bataille, Laetitia [1 ]
Delon, Isabelle [2 ,3 ]
Da Ponte, Jean Philippe [1 ]
Brown, Nicholas H. [2 ,3 ]
Jagla, Krzysztof [1 ]
机构
[1] Univ Clermont Ferrand, CNRS, INSERM, GReD,UMR6247,U931, F-63000 Clermont Ferrand, France
[2] Univ Cambridge, Gurdon Inst, Cambridge CB2 1QN, England
[3] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 1QN, England
基金
英国生物技术与生命科学研究理事会;
关键词
MYOBLAST FUSION; F-SPONDIN; DROSOPHILA EMBRYOGENESIS; ADAPTER PROTEIN; SOMATIC MUSCLES; CELL FATES; PAXILLIN; EXPRESSION; MYOGENESIS; DIVERSIFICATION;
D O I
10.1016/j.devcel.2010.07.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In all metazoan organisms, the diversification of cell types involves determination of cell fates and subsequent execution of specific differentiation programs. During Drosophila myogenesis, identity genes specify the fates of founder myoblasts, from which derive all individual larval muscles. Here, to understand how cell fate information residing within founders is translated during differentiation, we focus on three identity genes, eve, lb, and slou, and how they control the size of individual muscles by regulating the number of fusion events. They achieve this by setting expression levels of Mp20, Pax, and mspo, three genes that regulate actin dynamics and cell adhesion and, as we show here, modulate the fusion process in a muscle-specific manner. Thus, these data show how the identity information implemented by transcription factors is translated via target genes into cell-type-specific programs of differentiation.
引用
收藏
页码:317 / 328
页数:12
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