衰老和阿尔茨海默病中的大脑体细胞突变。

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY Annual review of genomics and human genetics Pub Date : 2021-08-31 Epub Date: 2021-05-12 DOI:10.1146/annurev-genom-121520-081242
Michael B Miller, Hannah C Reed, Christopher A Walsh
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引用次数: 27

摘要

体细胞突变发生在合子后,在一个有机体的细胞之间产生遗传差异。体细胞突变作为癌症的驱动因素,在非肿瘤细胞中也存在,包括在大脑中。核酸测序技术的进步使最近的突破阐明了体细胞突变在衰老和大脑退行性疾病中的作用。体细胞突变在人类神经元的衰老过程中积累,这一过程被称为基因衰老。最近的一些研究主要是从引起家族性阿尔茨海默病的基因的角度研究了阿尔茨海默病(AD)的体细胞突变。我们还获得了关于全基因组突变的新信息,提供了对驱动体细胞突变和细胞功能障碍的细胞事件的见解。本文综述了最近的概念、方法和研究进展,以了解大脑体细胞突变在衰老和阿尔茨海默病中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Brain Somatic Mutation in Aging and Alzheimer's Disease.

Somatic mutations arise postzygotically, producing genetic differences between cells in an organism. Well established as a driver of cancer, somatic mutations also exist in nonneoplastic cells, including in the brain. Technological advances in nucleic acid sequencing have enabled recent breakthroughs that illuminate the roles of somatic mutations in aging and degenerative diseases of the brain. Somatic mutations accumulate during aging in human neurons, a process termed genosenium. A number of recent studies have examined somatic mutations in Alzheimer's disease (AD), primarily from the perspective of genes causing familial AD. We have also gained new information on genome-wide mutations, providing insights into the cellular events driving somatic mutation and cellular dysfunction. This review highlights recent concepts, methods, and findings in the progress to understand the role of brain somatic mutation in aging and AD.

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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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