Department of Anatomy, University of Otago, New Zealand.
Genome Biol Evol. 2017 Sep 1;9(9):2428-2443. doi: 10.1093/gbe/evx164.
Microsatellite repeat DNA is best known for its length mutability, which is implicated in several neurological diseases and cancers, and often exploited as a genetic marker. Less well-known is the body of work exploring the widespread and surprisingly diverse functional roles of microsatellites. Recently, emerging evidence includes the finding that normal microsatellite polymorphism contributes substantially to the heritability of human gene expression on a genome-wide scale, calling attention to the task of elucidating the mechanisms involved. At present, these are underexplored, but several themes have emerged. I review evidence demonstrating roles for microsatellites in modulation of transcription factor binding, spacing between promoter elements, enhancers, cytosine methylation, alternative splicing, mRNA stability, selection of transcription start and termination sites, unusual structural conformations, nucleosome positioning and modification, higher order chromatin structure, noncoding RNA, and meiotic recombination hot spots.
微卫星重复 DNA 以其长度易变性而闻名,这与几种神经疾病和癌症有关,通常被用作遗传标记。不太为人知的是,人们广泛探索了微卫星的功能作用,这些作用令人惊讶且多种多样。最近,新出现的证据包括发现正常的微卫星多态性在很大程度上导致了人类基因表达在全基因组范围内的遗传性,这引起了人们对阐明相关机制的关注。目前,这些机制还未得到充分探索,但已经出现了几个主题。我回顾了证明微卫星在转录因子结合、启动子元件、增强子、胞嘧啶甲基化、选择性剪接、mRNA 稳定性、转录起始和终止位点选择、异常结构构象、核小体定位和修饰、高级染色质结构、非编码 RNA 和减数分裂重组热点等方面的作用的证据。