The atypical Rac activator Dock180 (Dock1) regulates myoblast fusion in vivo

被引:134
作者
Laurin, Melanie [2 ,3 ]
Fradet, Nadine [2 ]
Blangy, Anne [4 ]
Hall, Alan [5 ]
Vuori, Kristiina [1 ]
Cote, Jean-Francois [2 ,3 ,6 ]
机构
[1] Burnham Inst Med Res, La Jolla, CA 92037 USA
[2] Inst Rech Clin Montreal, Montreal, PQ H2W 1R7, Canada
[3] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[4] CNRS, Ctr Rech & Biochim Macromol, F-34293 Montpellier, France
[5] Mem Sloan Kettering Canc Ctr, New York, NY 10065 USA
[6] McGill Univ, Div Expt Med, Montreal, PQ H3A 1A3, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
Dock5; mouse model; myogenesis; Myoblast City;
D O I
10.1073/pnas.0805546105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dock1 (also known as Dock180) is a prototypical member of a new family of atypical Rho GTPase activators. Genetic studies in Drosophila and Caenorhabditis elegans have demonstrated that Dock1 orthologues in these organisms have a crucial role in activating Rac GTPase signaling. We generated mutant alleles of the closely related Dock1 and Dock5 genes to study their function in mammals. We report that while Dock5 is dispensable for normal mouse embryogenesis, Dock1 has an essential role in embryonic development. A dramatic reduction of all skeletal muscle tissues is observed in Dock1-null embryos. Mechanistically, this embryonic defect is attributed to a strong deficiency in myoblast fusion, which is detectable both in vitro and in vivo. Furthermore, we have uncovered a contribution of Dock5 toward myofiber development. These studies identify Dock1 and Dock5 as critical regulators of the fusion step during primary myogenesis in mammals and demonstrate that a specific component of the myoblast fusion machinery identified in Drosophila plays an evolutionarily conserved role in higher vertebrates.
引用
收藏
页码:15446 / 15451
页数:6
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