Suppr超能文献

调控骨骼肌分化、生长和稳态的转录机制。

Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis.

机构信息

Max-Planck-Institute for Heart and Lung Research, Department for Cardiac Development and Remodelling, Benekestrasse, Bad Nauheim, Germany. thomas.braun@ mpi-bn.mpg.de

出版信息

Nat Rev Mol Cell Biol. 2011 Jun;12(6):349-61. doi: 10.1038/nrm3118.

Abstract

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.

摘要

骨骼肌是运动和能量代谢的主要器官系统。出生后的肌肉主要通过重塑现有的纤维来生长和适应,而胚胎中的肌肉则通过成肌细胞的增殖来生长。最近,控制脊椎动物肌肉发育的成肌转录因子的遗传层次结构——通过成肌细胞的增殖、迁移、融合和功能适应到快肌和慢肌纤维——变得更加清晰。控制出生后肥大生长、重塑和功能分化的转录机制与血清反应因子(SRF)、JUNB 和叉头框蛋白 O3A(FOXO3A)一起重新部署成肌因子。此外,在发育和出生后重塑过程中,microRNAs 的广泛转录后调控作用也已显现。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验