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体内三核苷酸重复序列不稳定性的特征

Features of trinucleotide repeat instability in vivo.

作者信息

Kovtun Irina V, McMurray Cynthia T

机构信息

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, 200 First Street, SW, Rochester, MN 55905, USA.

出版信息

Cell Res. 2008 Jan;18(1):198-213. doi: 10.1038/cr.2008.5.

Abstract

Unstable repeats are associated with various types of cancer and have been implicated in more than 40 neurodegenerative disorders. Trinucleotide repeats are located in non-coding and coding regions of the genome. Studies of bacteria, yeast, mice and man have helped to unravel some features of the mechanism of trinucleotide expansion. Looped DNA structures comprising trinucleotide repeats are processed during replication and/or repair to generate deletions or expansions. Most in vivo data are consistent with a model in which expansion and deletion occur by different mechanisms. In mammals, microsatellite instability is complex and appears to be influenced by genetic, epigenetic and developmental factors.

摘要

不稳定重复序列与多种类型的癌症相关,并且已被认为与40多种神经退行性疾病有关。三核苷酸重复序列位于基因组的非编码区和编码区。对细菌、酵母、小鼠和人类的研究有助于揭示三核苷酸扩增机制的一些特征。包含三核苷酸重复序列的环状DNA结构在复制和/或修复过程中被加工,从而产生缺失或扩增。大多数体内数据与一种模型一致,即扩增和缺失通过不同机制发生。在哺乳动物中,微卫星不稳定性很复杂,似乎受遗传、表观遗传和发育因素的影响。

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