Fishel R, Derbyshire M K, Moore S P, Young C S
Laboratory of Chromosome Biology, NCI-Frederick Cancer Research and Development Center, Maryland 21702.
Biochimie. 1991 Feb-Mar;73(2-3):257-67. doi: 10.1016/0300-9084(91)90211-i.
Purified and partially purified protein fractions from human cells have been developed that promote homologous and nonhomologous recombination reactions in vitro. Homologous pairing of model DNA substrates is catalyzed by the homologous pairing protein HPP-1 in a magnesium-dependent, ATP-independent reaction that requires stoichiometric amounts of the protein. Addition of the human single-strand binding (SSB) holoprotein complex hRP-A reduces the requirement of HPP-1 in the reaction up to 20-fold. Although the combination of homologous pairing and SSB activities is similar to the bacterial strand-exchange process, the numbers, size, and requirements of the human reaction appear to preclude any detailed comparisons. We have used Z-DNA affinity chromatography as a major step in isolation of human recombination proteins and found that the activities appear to elute as a complex form in approximate multiples of 500 kDa. Associated with the homologous recombination complex is a potent blunt-end ligation activity that appears to mimic the nonhomologous joining functions that are frequently seen following transfection of DNA into mammalian cells. A simple scheme for the association of homologous and nonhomologous recombination functions in mammalian cells is discussed.
已开发出从人类细胞中纯化和部分纯化的蛋白质组分,它们可在体外促进同源和非同源重组反应。模型DNA底物的同源配对由同源配对蛋白HPP-1催化,该反应依赖镁离子、不依赖ATP,且需要化学计量的该蛋白。添加人类单链结合(SSB)全蛋白复合物hRP-A可将反应中对HPP-1的需求降低多达20倍。尽管同源配对和SSB活性的组合类似于细菌的链交换过程,但人类反应的数量、大小和需求似乎排除了任何详细的比较。我们已将Z-DNA亲和色谱法作为分离人类重组蛋白的主要步骤,发现这些活性似乎以约500 kDa倍数的复合形式洗脱。与同源重组复合物相关的是一种强大的平端连接活性,它似乎模拟了将DNA转染到哺乳动物细胞后常见的非同源连接功能。文中讨论了哺乳动物细胞中同源和非同源重组功能关联的简单模式。