A calcineurin-dependent transcriptional pathway controls skeletal muscle fiber type

被引:809
|
作者
Chin, ER
Olson, EN
Richardson, JA
Yano, Q
Humphries, C
Shelton, JM
Wu, H
Zhu, WG
Bassel-Duby, R
Williams, RS [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75235 USA
[2] Univ Texas, SW Med Ctr, Dept Mol Biol Oncol, Dallas, TX 75235 USA
[3] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX 75235 USA
关键词
myosin; myoglobin; NFAT; MEF2; cyclosporin A; exercise;
D O I
10.1101/gad.12.16.2499
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Slow- and fast-twitch myofibers of adult skeletal muscles express unique sets of muscle-specific genes, and these distinctive programs of gene expression are controlled by variations in motor neuron activity. It is well established that, as a consequence of more frequent neural stimulation, slow fibers maintain higher levels of intracellular free calcium than fast fibers, but the mechanisms by which calcium may function as a messenger linking nerve activity to changes in gene expression in skeletal muscle have been unknown. Here, fiber-type-specific gene expression in skeletal muscles is shown to be controlled by a signaling pathway that involves calcineurin, a cyclosporin-sensitive, calcium-regulated serine/threonine phosphatase. Activation of calcineurin in skeletal myocytes selectively up-regulates slow-fiber-specific gene promoters. Conversely, inhibition of calcineurin activity by administration of cyclosporin A to intact animals promotes slow-to-fast fiber transformation. Transcriptional activation of slow-fiber-specific transcription appears to be mediated by a combinatorial mechanism involving proteins of the NFAT and MEF2 families. These results identify a molecular mechanism by which different patterns of motor nerve activity promote selective changes in gene expression to establish the specialized characteristics of slow and fast myofibers.
引用
收藏
页码:2499 / 2509
页数:11
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