Suppr超能文献

线粒体动态:分子机制、相关原发性线粒体疾病和治疗方法。

Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic Approaches.

机构信息

Laboratory of Molecular Medicine, Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

出版信息

Genes (Basel). 2021 Feb 10;12(2):247. doi: 10.3390/genes12020247.

Abstract

Mitochondria do not exist as individual entities in the cell-conversely, they constitute an interconnected community governed by the constant and opposite process of fission and fusion. The mitochondrial fission leads to the formation of smaller mitochondria, promoting the biogenesis of new organelles. On the other hand, following the fusion process, mitochondria appear as longer and interconnected tubules, which enhance the communication with other organelles. Both fission and fusion are carried out by a small number of highly conserved guanosine triphosphatase proteins and their interactors. Disruption of this equilibrium has been associated with several pathological conditions, ranging from cancer to neurodegeneration, and mutations in genes involved in mitochondrial fission and fusion have been reported to be the cause of a subset of neurogenetic disorders.

摘要

线粒体在细胞中并不以独立实体的形式存在——相反,它们构成了一个相互关联的共同体,受分裂和融合这两个相反过程的持续调控。线粒体的分裂导致较小的线粒体的形成,促进新细胞器的生物发生。另一方面,在融合过程之后,线粒体呈现出更长且相互连接的小管,这增强了与其他细胞器的交流。分裂和融合都是由少数高度保守的鸟苷三磷酸酶蛋白及其相互作用蛋白来执行的。这种平衡的破坏与多种病理状况有关,从癌症到神经退行性疾病都有涉及,并且已经报道了与线粒体分裂和融合相关的基因的突变是一组神经遗传疾病的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfe2/7916359/82941b5da3c2/genes-12-00247-g001.jpg

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