Expanding horizons of tandem repeats in biology and medicine: Why 'genomic dark matter' matters.

IF 3.4 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anthony J Hannan
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Abstract

Approximately half of the human genome includes repetitive sequences, and these DNA sequences (as well as their transcribed repetitive RNA and translated amino-acid repeat sequences) are known as the repeatome. Within this repeatome there are a couple of million tandem repeats, dispersed throughout the genome. These tandem repeats have been estimated to constitute ∼8% of the entire human genome. These tandem repeats can be located throughout exons, introns and intergenic regions, thus potentially affecting the structure and function of tandemly repetitive DNA, RNA and protein sequences. Over more than three decades, more than 60 monogenic human disorders have been found to be caused by tandem-repeat mutations. These monogenic tandem-repeat disorders include Huntington's disease, a variety of ataxias, amyotrophic lateral sclerosis and frontotemporal dementia, as well as many other neurodegenerative diseases. Furthermore, tandem-repeat disorders can include fragile X syndrome, related fragile X disorders, as well as other neurological and psychiatric disorders. However, these monogenic tandem-repeat disorders, which were discovered via their dominant or recessive modes of inheritance, may represent the 'tip of the iceberg' with respect to tandem-repeat contributions to human disorders. A previous proposal that tandem repeats may contribute to the 'missing heritability' of various common polygenic human disorders has recently been supported by a variety of new evidence. This includes genome-wide studies that associate tandem-repeat mutations with autism, schizophrenia, Parkinson's disease and various types of cancers. In this article, I will discuss how tandem-repeat mutations and polymorphisms could contribute to a wide range of common disorders, along with some of the many major challenges of tandem-repeat biology and medicine. Finally, I will discuss the potential of tandem repeats to be therapeutically targeted, so as to prevent and treat an expanding range of human disorders.

拓展串联重复序列在生物学和医学中的应用:为什么 "基因组暗物质 "很重要?
人类基因组约有一半包含重复序列,这些 DNA 序列(及其转录的重复 RNA 和翻译的氨基酸重复序列)被称为重复序列组。在重复序列组中,有几百万个串联重复序列分布在整个基因组中。据估计,这些串联重复序列占整个人类基因组的 8%。这些串联重复序列遍布外显子、内含子和基因间区域,因此可能影响串联重复 DNA、RNA 和蛋白质序列的结构和功能。30 多年来,已发现有 60 多种单基因人类疾病是由串联重复突变引起的。这些单基因串联重复疾病包括亨廷顿氏病、各种共济失调、肌萎缩侧索硬化症和额颞叶痴呆症,以及许多其他神经退行性疾病。此外,串联重复疾病还包括脆性 X 综合征、相关的脆性 X 疾病以及其他神经和精神疾病。然而,这些通过显性或隐性遗传方式发现的单基因串联重复疾病可能只是串联重复对人类疾病影响的 "冰山一角"。串联重复基因可能导致各种常见多基因人类疾病的 "缺失遗传性",这一说法最近得到了各种新证据的支持。这包括将串联重复序列突变与自闭症、精神分裂症、帕金森病和各种癌症联系起来的全基因组研究。在这篇文章中,我将讨论串联重复突变和多态性如何可能导致各种常见疾病,以及串联重复生物学和医学面临的一些重大挑战。最后,我将讨论串联重复序列成为治疗目标的潜力,从而预防和治疗越来越多的人类疾病。
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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来源期刊
CiteScore
7.70
自引率
0.00%
发文量
94
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