Enomoto Rima, Kinebuchi Takashi, Sato Makoto, Yagi Hideshi, Kurumizaka Hitoshi, Yokoyama Shigeyuki
RIKEN Genomic Sciences Center, 1-7-22 Suehiro-cho, Tsurumi, Yokohama 230-0045, Japan.
J Biol Chem. 2006 Mar 3;281(9):5575-81. doi: 10.1074/jbc.M506506200. Epub 2006 Jan 9.
In Saccharomyces cerevisiae, the Hop2 protein forms a complex with the Mnd1 protein and is required for the alignment of homologous chromosomes during meiosis, probably through extensive homology matching between them. The Rad51 and Dmc1 proteins, the eukaryotic RecA orthologs, promote strand exchange and may function in the extensive matching of homology within paired DNA molecules. In the present study, we purified the human TBPIP/Hop2-Mnd1 complex and found that it significantly stimulates the Dmc1- and Rad51-mediated strand exchange. The human Hop2-Mnd1 complex preferentially binds to a three-stranded DNA branch, which mimics the strand-exchange intermediate. These findings are consistent with genetic data, which showed that the Hop2 and Mnd1 proteins are required for homology matching between homologous chromosomes. Therefore, the human TBPIP/Hop2-Mnd1 complex may ensure proper pairing between homologous chromosomes through its stimulation of strand exchange during meiosis.
在酿酒酵母中,Hop2蛋白与Mnd1蛋白形成复合物,在减数分裂过程中同源染色体的配对中发挥作用,可能是通过它们之间广泛的同源性匹配来实现。Rad51和Dmc1蛋白是真核生物RecA的直系同源物,促进链交换,并可能在配对DNA分子内的同源性广泛匹配中发挥作用。在本研究中,我们纯化了人TBPIP/Hop2-Mnd1复合物,发现它能显著刺激Dmc1和Rad51介导的链交换。人Hop2-Mnd1复合物优先结合三链DNA分支,该分支模拟链交换中间体。这些发现与遗传数据一致,遗传数据表明Hop2和Mnd1蛋白是同源染色体之间同源性匹配所必需的。因此,人TBPIP/Hop2-Mnd1复合物可能通过在减数分裂过程中刺激链交换来确保同源染色体之间的正确配对。