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酿酒酵母MSH2是一种错配碱基识别蛋白,它也能识别DNA中的霍利迪连接体。

Saccharomyces cerevisiae MSH2, a mispaired base recognition protein, also recognizes Holliday junctions in DNA.

作者信息

Alani E, Lee S, Kane M F, Griffith J, Kolodner R D

机构信息

Section of Genetics and Development, Cornell University, Ithaca, NY 14853-2703, USA.

出版信息

J Mol Biol. 1997 Jan 24;265(3):289-301. doi: 10.1006/jmbi.1996.0743.

Abstract

Genetic and biochemical studies have suggested that mismatch repair proteins interact with recombination intermediates to prevent recombination, or to limit the extent of formation of heteroduplex DNA during recombination between divergent DNA sequences. To test the idea that mismatch repair proteins regulate recombination by interacting with recombination intermediates, we investigated whether the Saccharomyces cerevisiae MutS homolog MSH2 could interact with Holliday junctions. Both filter-binding and electron-microscopic analysis showed that MSH2 bound to duplex DNA molecules containing Holliday junctions with a higher affinity than to control duplex DNA, single-stranded DNA or a control duplex DNA containing a mispaired base. The MSH2-Holliday junction complexes were also more stable than MSH2-duplex DNA complexes. This observation suggests that MSH2 protein could directly coordinate the interaction between mismatch repair and genetic recombination observed in genetic studies.

摘要

遗传和生化研究表明,错配修复蛋白与重组中间体相互作用,以防止重组,或在不同DNA序列之间的重组过程中限制异源双链DNA的形成程度。为了验证错配修复蛋白通过与重组中间体相互作用来调节重组这一观点,我们研究了酿酒酵母MutS同源物MSH2是否能与霍利迪连接体相互作用。滤膜结合分析和电子显微镜分析均表明,MSH2与含有霍利迪连接体的双链DNA分子结合的亲和力高于对照双链DNA、单链DNA或含有错配碱基的对照双链DNA。MSH2-霍利迪连接体复合物也比MSH2-双链DNA复合物更稳定。这一观察结果表明,MSH2蛋白可能直接协调遗传研究中观察到的错配修复与基因重组之间的相互作用。

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