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小同源序列在基因组结构变异中的作用。

The role of microhomology in genomic structural variation.

机构信息

Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, E1 2AT, UK.

Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, E1 2AT, UK.

出版信息

Trends Genet. 2014 Mar;30(3):85-94. doi: 10.1016/j.tig.2014.01.001. Epub 2014 Feb 4.

Abstract

Genomic structural variation, which can be defined as differences in the copy number, orientation, or location of relatively large DNA segments, is not only crucial in evolution, but also gives rise to genomic disorders. Whereas the major mechanisms that generate structural variation have been well characterised, insights into additional mechanisms are emerging from the identification of short regions of DNA sequence homology, also known as microhomology, at chromosomal breakpoints. In addition, functional studies are elucidating the characteristics of microhomology-mediated pathways, which are mutagenic. Here, we describe the features and mechanistic models of microhomology-mediated events, discuss their physiological and pathological significance, and highlight recent advances in this rapidly evolving field of research.

摘要

基因组结构变异可定义为相对较大的 DNA 片段的拷贝数、方向或位置的差异,它不仅在进化中至关重要,而且还会导致基因组疾病。虽然已经很好地描述了产生结构变异的主要机制,但通过鉴定染色体断裂点处也称为微同源性的短 DNA 序列同源性区域,人们对其他机制的认识也在不断涌现。此外,功能研究阐明了具有突变性的微同源介导途径的特征。在这里,我们描述了微同源介导事件的特征和机制模型,讨论了它们的生理和病理意义,并强调了这一快速发展的研究领域的最新进展。

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