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肌营养不良蛋白通过微小RNA调控肌肉细胞的表观遗传特征。

Dystrophin Orchestrates the Epigenetic Profile of Muscle Cells Via miRNAs.

作者信息

Marrone April K, Shcherbata Halyna R

机构信息

Max Planck Research Group of Gene Expression and Signaling, Max Planck Institute for Biophysical Chemistry Goettingen, Germany.

出版信息

Front Genet. 2011 Sep 13;2:64. doi: 10.3389/fgene.2011.00064. eCollection 2011.

Abstract

Mammalian musculature is a very robust and dynamic tissue that goes through many rounds of degeneration and regeneration in an individual's lifetime. There is a biological program that maintains muscle progenitor cells that, when activated, give rise to intermediate myoblast progeny that consequently differentiate into mature muscle cells. Recent works have provided a picture of the role that microRNAs (miRNAs) play in maintaining aspects of this program. Intriguingly, a subset of these miRNAs is de-regulated in muscular dystrophies (MDs), a group of fatal inherited neuromuscular disorders that are often associated with deficiencies in the Dystrophin (Dys) complex. Apparently, transcriptional expression of many of the muscle specific genes and miRNAs is dependent on chromatin state regulated by the Dys-Syn-nNOS pathway. This puts Dystrophin at the epicenter of a highly regulated program of muscle gene expression in which miRNAs help to coordinate networking between multiple phases of muscle maintenance, degeneration, and regeneration. Therefore, understanding the role of miRNAs in physiology of normal and diseased muscle tissue could be useful for future applications in improving the MD therapies and could open new clinical perspectives.

摘要

哺乳动物的肌肉组织是一种非常强健且具有动态变化的组织,在个体的一生中会经历多轮退化和再生。存在一种生物学程序来维持肌肉祖细胞,这些祖细胞被激活后会产生中间成肌细胞后代,进而分化为成熟的肌肉细胞。近期的研究揭示了微小RNA(miRNA)在维持该程序的各个方面所起的作用。有趣的是,这些miRNA中的一部分在肌肉营养不良症(MD)中表达失调,MD是一组致命的遗传性神经肌肉疾病,通常与肌营养不良蛋白(Dys)复合体的缺陷有关。显然,许多肌肉特异性基因和miRNA的转录表达依赖于由Dys - Syn - nNOS途径调控的染色质状态。这使得肌营养不良蛋白处于肌肉基因表达高度调控程序的核心位置,其中miRNA有助于协调肌肉维持、退化和再生多个阶段之间的网络联系。因此,了解miRNA在正常和患病肌肉组织生理学中的作用,可能有助于未来改进MD治疗方法,并开拓新的临床前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1224/3268617/290f1ed2f2b0/fgene-02-00064-g001.jpg

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