Gupta R C, Bazemore L R, Golub E I, Radding C M
Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, USA.
Proc Natl Acad Sci U S A. 1997 Jan 21;94(2):463-8. doi: 10.1073/pnas.94.2.463.
Homologous pairing and strand exchange, which are catalyzed by Escherichia coli RecA protein, are central to homologous recombination. Homologs of this protein are found in eukaryotes; however, little has been reported on the recombinase activities of the mammalian homologs, including the human protein, denoted HsRad51. For the studies described here, we purified HsRad51 form E. coli. Although the activities of HsRad51 and RecA were qualitatively similar in the presence of ATP, there were also striking differences. The stoichiometry of binding to DNA and the rate of renaturation of complementary strands were similar for the two proteins, but rates of ATP hydrolysis, homologous pairing, and subsequent strand exchange promoted by HsRad51 were less than 1/10 those of RecA. In addition, HsRad51 bound gamma-thio-ATP and formed stable presynaptic complexes that promoted renaturation as rapidly as RecA, but the recombinant human protein catalyzed neither strand exchange nor homologous pairing of a single strand with duplex DNA in the presence of the ATP analog. By contrast, RecA promoted both of the latter reactions in control experiments. These observations suggest that among RecA-like proteins, HsRad51 may be a variant in which homologous pairing and strand exchange are more closely linked to the hydrolysis of ATP.
由大肠杆菌RecA蛋白催化的同源配对和链交换是同源重组的核心。在真核生物中发现了该蛋白的同源物;然而,关于包括人类蛋白HsRad51在内的哺乳动物同源物的重组酶活性,报道甚少。对于此处所述的研究,我们从大肠杆菌中纯化了HsRad51。尽管在ATP存在的情况下,HsRad51和RecA的活性在性质上相似,但也存在显著差异。两种蛋白质与DNA结合的化学计量以及互补链复性的速率相似,但HsRad51促进的ATP水解、同源配对和随后的链交换速率不到RecA的1/10。此外,HsRad51结合γ-硫代-ATP并形成稳定的突触前复合物,其促进复性的速度与RecA一样快,但在ATP类似物存在的情况下,重组人类蛋白既不催化链交换,也不催化单链与双链DNA的同源配对。相比之下,在对照实验中,RecA促进了后两种反应。这些观察结果表明,在RecA样蛋白中,HsRad51可能是一种变体,其中同源配对和链交换与ATP水解的联系更为紧密。