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三核苷酸重复扩展由人类无细胞提取物催化。

Trinucleotide repeat expansions catalyzed by human cell-free extracts.

机构信息

Centre for Chromosome Biology, School of Natural Sciences, National University of Ireland Galway, Distillery Road, Galway, Ireland.

出版信息

Cell Res. 2013 Apr;23(4):565-72. doi: 10.1038/cr.2013.12. Epub 2013 Jan 22.

DOI:10.1038/cr.2013.12
PMID:23337586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3616437/
Abstract

Trinucleotide repeat expansions cause 17 heritable human neurological disorders. In some diseases, somatic expansions occur in non-proliferating tissues such as brain where DNA replication is limited. This finding stimulated significant interest in replication-independent expansion mechanisms. Aberrant DNA repair is a likely source, based in part on mouse studies showing that somatic expansions are provoked by the DNA repair protein MutSβ (Msh2-Msh3 complex). Biochemical studies to date used cell-free extracts or purified DNA repair proteins to yield partial reactions at triplet repeats. The findings included expansions on one strand but not the other, or processing of DNA hairpin structures thought to be important intermediates in the expansion process. However, it has been difficult to recapitulate complete expansions in vitro, and the biochemical role of MutSβ remains controversial. Here, we use a novel in vitro assay to show that human cell-free extracts catalyze expansions and contractions of trinucleotide repeats without the requirement for DNA replication. The extract promotes a size range of expansions that is similar to certain diseases, and triplet repeat length and sequence govern expansions in vitro as in vivo. MutSβ stimulates expansions in the extract, consistent with aberrant repair of endogenous DNA damage as a source of expansions. Overall, this biochemical system retains the key characteristics of somatic expansions in humans and mice, suggesting that this important mutagenic process can be restored in the test tube.

摘要

三核苷酸重复扩展导致 17 种可遗传的人类神经疾病。在某些疾病中,体细胞扩展发生在非增殖组织中,如大脑,其中 DNA 复制受到限制。这一发现激发了人们对非复制依赖性扩展机制的极大兴趣。异常的 DNA 修复可能是一个来源,部分基于小鼠研究表明,体细胞扩展是由 DNA 修复蛋白 MutSβ(Msh2-Msh3 复合物)引发的。迄今为止的生化研究使用无细胞提取物或纯化的 DNA 修复蛋白在三核苷酸重复序列中产生部分反应。这些发现包括一条链上的扩展,但另一条链上没有,或者处理 DNA 发夹结构,这些结构被认为是扩展过程中的重要中间体。然而,很难在体外重现完整的扩展,MutSβ 的生化作用仍然存在争议。在这里,我们使用一种新的体外测定法表明,人类无细胞提取物在不需要 DNA 复制的情况下催化三核苷酸重复的扩展和收缩。该提取物促进了类似于某些疾病的三核苷酸重复扩展范围,并且三核苷酸重复长度和序列在体外和体内控制扩展。MutSβ 刺激提取物中的扩展,与内源性 DNA 损伤的异常修复作为扩展的来源一致。总的来说,这个生化系统保留了人类和小鼠体细胞扩展的关键特征,表明这种重要的诱变过程可以在试管中恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/1d9b2101e998/cr201312f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/f619154f0cad/cr201312f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/bd34a7310756/cr201312f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/bf148876a981/cr201312f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/9f49c976a4dc/cr201312f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/1d9b2101e998/cr201312f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/f619154f0cad/cr201312f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/bd34a7310756/cr201312f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/bf148876a981/cr201312f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/9f49c976a4dc/cr201312f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f39/3616437/1d9b2101e998/cr201312f5.jpg

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本文引用的文献

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