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酵母线粒体蛋白MSH1的纯化与特性分析,该蛋白可与DNA错配结合。

Purification and characterization of MSH1, a yeast mitochondrial protein that binds to DNA mismatches.

作者信息

Chi N W, Kolodner R D

机构信息

Division of Cellular and Molecular Biology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115.

出版信息

J Biol Chem. 1994 Nov 25;269(47):29984-92.

PMID:7961998
Abstract

MSH1 is a homologue of the Escherichia coli MutS gene that is proposed to play an important role in the repair and maintenance of mitochondrial DNA in Saccharomyces cerevisiae (Reenan, R.A., and Kolodner, R. D. (1992) Genetics 132, 985-1985). In this study, we demonstrate that msh1/MSH1 strains accumulate point mutations in mitochondria seven times faster than the wild-type. We also show that the MSH1 protein is targeted to the mitochondria where its mitochondrial-targeting sequence is removed. Purified MSH1 hydrolyzes ATP and recognizes DNA substrates containing nucleotide mismatches and unpaired nucleotides. The hierarchy of binding affinity of MSH1 among various mismatches is similar to that of MutS, suggesting that both proteins share a highly conserved scheme for recognizing mismatches. The specific binding of MSH1 to mismatches is more resistant to NaCl inhibition and has a slower dissociation rate as compared to the nonspecific binding to complementary DNA sequences. Our data support the idea that MSH1 plays a role in eliminating biosynthetic errors and homeologous recombination in mitochondrial genome by recognizing premutagenic DNA mismatches.

摘要

MSH1是大肠杆菌MutS基因的同源物,据推测它在酿酒酵母线粒体DNA的修复和维持中起重要作用(Reenan, R.A., and Kolodner, R. D. (1992) Genetics 132, 985 - 1985)。在本研究中,我们证明msh1/MSH1菌株线粒体中积累点突变的速度比野生型快七倍。我们还表明,MSH1蛋白定位于线粒体,其线粒体靶向序列在那里被去除。纯化的MSH1水解ATP,并识别含有核苷酸错配和未配对核苷酸的DNA底物。MSH1在各种错配之间的结合亲和力层次与MutS相似,这表明两种蛋白质在识别错配方面具有高度保守的机制。与对互补DNA序列的非特异性结合相比,MSH1对错配的特异性结合对NaCl抑制更具抗性,并且解离速率更慢。我们的数据支持这样的观点,即MSH1通过识别诱变前的DNA错配,在消除线粒体基因组中的生物合成错误和同源重组中发挥作用。

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