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Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis.

机译:调节骨骼肌分化,生长和体内稳态的转录机制。

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摘要

Skeletal muscle is the dominant organ system in locomotion and energy metabolism. Postnatal muscle grows and adapts largely by remodelling pre-existing fibres, whereas embryonic muscle grows by the proliferation of myogenic cells. Recently, the genetic hierarchies of the myogenic transcription factors that control vertebrate muscle development - by myoblast proliferation, migration, fusion and functional adaptation into fast-twitch and slow-twitch fibres - have become clearer. The transcriptional mechanisms controlling postnatal hypertrophic growth, remodelling and functional differentiation redeploy myogenic factors in concert with serum response factor (SRF), JUNB and forkhead box protein O3A (FOXO3A). It has also emerged that there is extensive post-transcriptional regulation by microRNAs in development and postnatal remodelling.
机译:骨骼肌是运动和能量代谢的主要器官系统。出生后的肌肉通过重塑已有的纤维而生长并在很大程度上适应,而胚胎肌肉则通过成肌细胞的增殖而生长。最近,控制脊椎动物肌肉发育的成肌转录因子的遗传层次-通过成肌细胞的增殖,迁移,融合和向快速抽动和慢速抽动纤维的功能适应-变得更加清晰。控制产后肥大性生长,重塑和功能分化的转录机制与血清反应因子(SRF),JUNB和叉头盒蛋白O3A(FOXO3A)一起重新部署了肌源性因子。还已经发现,在发育和产后重塑中,microRNA具有广泛的转录后调控。

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