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线粒体DNA耗竭:综合征与基因

Depletion of mtDNA: syndromes and genes.

作者信息

Alberio Simona, Mineri Rossana, Tiranti Valeria, Zeviani Massimo

机构信息

Unit of Molecular Neurogenetics-Pierfranco and Luisa Mariani Center for the Study of Children's Mitochondrial Disorders, C. Besta Neurological Institute Foundation, IRCCS, Italy.

出版信息

Mitochondrion. 2007 Feb-Apr;7(1-2):6-12. doi: 10.1016/j.mito.2006.11.010. Epub 2006 Dec 5.

Abstract

Maintenance of mitochondrial DNA (mtDNA) requires the concerted activity of several nuclear-encoded factors that participate in its replication, being part of the mitochondrial replisome or ensuring the balanced supply of dNTPs to mitochondria. In the past decade, a growing number of syndromes associated with dysfunction due to tissue-specific depletion of mtDNA (MDS) have been reported. This article reviews the current knowledge of the genes responsible for these disorders, the impact of different mutations in the epidemiology of MDS and their role in the pathogenic mechanisms underlying the different clinical presentations.

摘要

线粒体DNA(mtDNA)的维持需要几种核编码因子的协同作用,这些因子参与其复制,是线粒体复制体的一部分或确保向线粒体平衡供应脱氧核苷酸三磷酸(dNTPs)。在过去十年中,越来越多与mtDNA组织特异性耗竭导致的功能障碍相关的综合征(线粒体DNA耗竭综合征,MDS)被报道。本文综述了目前对导致这些疾病的基因的认识、不同突变在MDS流行病学中的影响及其在不同临床表现潜在致病机制中的作用。

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