Sigurdsson S, Trujillo K, Song B, Stratton S, Sung P
Department of Molecular Medicine and Institute of Biotechnology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78245-3207, USA.
J Biol Chem. 2001 Mar 23;276(12):8798-806. doi: 10.1074/jbc.M010011200. Epub 2000 Dec 20.
Human Rad51 (hRad51), a member of a conserved family of general recombinases, is shown here to have an avid capability to make DNA joints between homologous DNA molecules and promote highly efficient DNA strand exchange of the paired molecules over at least 5.4 kilobase pairs. Furthermore, maximal efficiency of homologous DNA pairing and strand exchange is strongly dependent on the heterotrimeric single-stranded DNA binding factor hRPA and requires conditions that lessen interactions of the homologous duplex with the hRad51-single-stranded DNA nucleoprotein filament. The homologous DNA pairing and strand exchange system described should be valuable for dissecting the action mechanism of hRad51 and for deciphering its functional interactions with other recombination factors.
人源Rad51(hRad51)是保守的通用重组酶家族成员之一,本文显示其具有在同源DNA分子间形成DNA连接的强烈能力,并能促进配对分子间高效的DNA链交换,交换长度至少达5.4千碱基对。此外,同源DNA配对和链交换的最大效率强烈依赖于异源三聚体单链DNA结合因子hRPA,且需要减少同源双链与hRad51-单链DNA核蛋白丝相互作用的条件。所描述的同源DNA配对和链交换系统对于剖析hRad51的作用机制以及解读其与其他重组因子的功能相互作用应具有重要价值。