The B-cell maturation factor Blimp-1 specifies vertebrate slow-twitch muscle fiber identity in response to Hedgehog signaling

被引:152
作者
Baxendale, S
Davison, C
Muxworthy, C
Wolff, C
Ingham, PW
Roy, S
机构
[1] Univ Sheffield, Sch Med & Biomed Sci, Ctr Dev Genet, MRC Intecellular Signaling Grp, Sheffield S10 2TN, S Yorkshire, England
[2] Inst Mol & Cell Biol, Singapore 117609, Singapore
基金
英国医学研究理事会;
关键词
D O I
10.1038/ng1280
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Vertebrate skeletal muscles comprise distinct fiber types that differ in their morphology, contractile function, mitochondrial content and metabolic properties. Recent studies identified the transcriptional coactivator PGC-1 as a key mediator of the physiological stimuli that modulate fiber-type plasticity in postembryonic development(1). Although myoblasts become fated to differentiate into distinct kinds of fibers early in development, the identities of regulatory proteins that determine embryonic fiber-type specification are still obscure. Here we show that the gene u-boot (ubo), a mutation in which disrupts the induction of embryonic slow-twitch fibers(2), encodes the zebrafish homolog of Blimp-1, a SET domain containing transcription factor that promotes the terminal differentiation of B lymphocytes in mammals(3). Expression of ubo is induced by Hedgehog (Hh) signaling in prospective slow muscle precursors, and its activity alone is sufficient to direct slow-twitch fiber specific development by naive myoblasts. Our data provide the first molecular insight into the mechanism by which a specific group of muscle precursors is driven along a distinct pathway of fiber-type differentiation in response to positional cues in the vertebrate embryo.
引用
收藏
页码:88 / 93
页数:6
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