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B细胞成熟因子Blimp-1在响应刺猬信号通路时决定脊椎动物慢肌纤维的特性。

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

作者信息

Baxendale Sarah, Davison Claire, Muxworthy Claire, Wolff Christian, Ingham Philip W, Roy Sudipto

机构信息

MRC Intercellular Signaling Group, Center for Developmental Genetics, School of Medicine and Biomedical Sciences, University of Sheffield, Firth Court, Western Bank, Sheffield S10 2TN, UK.

出版信息

Nat Genet. 2004 Jan;36(1):88-93. doi: 10.1038/ng1280. Epub 2003 Dec 21.

Abstract

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-1alpha as a key mediator of the physiological stimuli that modulate fiber-type plasticity in postembryonic development. 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, encodes the zebrafish homolog of Blimp-1, a SET domain-containing transcription factor that promotes the terminal differentiation of B lymphocytes in mammals. 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.

摘要

脊椎动物的骨骼肌由不同的纤维类型组成,这些纤维在形态、收缩功能、线粒体含量和代谢特性方面存在差异。最近的研究表明,转录共激活因子PGC-1α是调节胚胎后发育中纤维类型可塑性的生理刺激的关键介质。尽管成肌细胞在发育早期就注定要分化为不同类型的纤维,但决定胚胎纤维类型特化的调节蛋白的身份仍然不清楚。在这里,我们表明基因u-boot(ubo),其突变会破坏胚胎慢肌纤维的诱导,编码斑马鱼中Blimp-1的同源物,Blimp-1是一种含有SET结构域的转录因子,可促进哺乳动物B淋巴细胞的终末分化。ubo的表达在前体慢肌前体细胞中由刺猬(Hh)信号诱导,其单独的活性足以指导未分化的成肌细胞进行慢肌纤维特异性发育。我们的数据首次从分子层面揭示了在脊椎动物胚胎中,特定的一组肌肉前体细胞如何响应位置线索而沿着不同的纤维类型分化途径发育的机制。

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