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串联重复基因组:串联重复多态性作为健康与疾病中遗传变异的动态来源

TRPing up the genome: Tandem repeat polymorphisms as dynamic sources of genetic variability in health and disease.

作者信息

Hannan Anthony J

机构信息

Howard Florey Institute, Florey Neuroscience Institutes, University of Melbourne, Melbourne, Victoria 3010, Australia.

出版信息

Discov Med. 2010 Oct;10(53):314-21.

Abstract

Repetitive DNA sequences constitute a large fraction of the genomes of humans and other animal species. Tandem repeats are a major class of repetitive DNA and the extent of their polymorphic distributions and functions within the human genome are only beginning to be explored. Tandem repeat polymorphisms (TRPs) provide a unique source of genomic variability and recent evidence suggests they can modulate a range of biological processes, in developing and mature organisms. Tandem repeats can change length during meiosis and mitosis, providing a dynamic source of genetic variation which may not only influence evolutionary processes, but also somatic cellular selection. Furthermore, recent evidence for post-mitotic instability of specific tandem repeats in neurons supports their additional possible roles in neuronal function and dysfunction. The mutation rate of TRPs is higher and the extent of polymorphism is far more diverse than that of single nucleotide polymorphisms (SNPs). Whereas SNPs are invariably binary in nature, TRPs generally exhibit extended digital (multiallelic) distributions, which provide a much richer range of polymorphic variants, and thus a wider possible range of genetic contribution to disease susceptibility. Expansions in tandem repeats are known to cause many monogenic disorders, which mainly affect the nervous system, including Huntington's disease, various spinocerebellar ataxias, other polyglutamine diseases, Friedreich ataxia, fragile X syndrome, myoclonic epilepsy, polyalanine disorders, and myotonic dystrophy. Furthermore, it has recently been proposed that TRPs could help solve the conundrum of "missing heritability" produced by SNP-based genome-wide association studies of various polygenic complex diseases. There are hundreds of thousands of unique tandem repeats in the human genome and their polymorphic distributions have the potential to greatly influence functional diversity and disease susceptibility. Recent discoveries in this expanding field are discussed, with a focus on the role of TRPs in brain development, function, and dysfunction.

摘要

重复DNA序列在人类和其他动物物种的基因组中占很大比例。串联重复序列是重复DNA的主要类别,其在人类基因组中的多态性分布范围和功能才刚刚开始被探索。串联重复多态性(TRPs)提供了基因组变异性的独特来源,最近的证据表明它们可以调节发育中和成熟生物体中的一系列生物学过程。串联重复序列在减数分裂和有丝分裂过程中可以改变长度,提供了遗传变异的动态来源,这不仅可能影响进化过程,还可能影响体细胞选择。此外,最近关于神经元中特定串联重复序列有丝分裂后不稳定性的证据支持了它们在神经元功能和功能障碍中的其他可能作用。TRPs的突变率更高,多态性程度比单核苷酸多态性(SNPs)要丰富得多。虽然SNPs本质上总是二元的,但TRPs通常表现出扩展的数字(多等位基因)分布,这提供了更丰富的多态性变体范围,因此对疾病易感性的遗传贡献范围也更广泛。已知串联重复序列的扩增会导致许多单基因疾病,主要影响神经系统,包括亨廷顿舞蹈症、各种脊髓小脑共济失调、其他多聚谷氨酰胺疾病、弗里德赖希共济失调、脆性X综合征、肌阵挛性癫痫、多聚丙氨酸疾病和强直性肌营养不良。此外,最近有人提出,TRPs有助于解决基于SNP的各种多基因复杂疾病全基因组关联研究产生的“遗传力缺失”难题。人类基因组中有数十万种独特的串联重复序列,它们的多态性分布有可能极大地影响功能多样性和疾病易感性。本文讨论了这个不断扩展领域中的最新发现,重点是TRPs在大脑发育、功能和功能障碍中的作用。

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