Sung P, Prakash L, Matson S W, Prakash S
Department of Biology, University of Rochester, NY 14627.
Proc Natl Acad Sci U S A. 1987 Dec;84(24):8951-5. doi: 10.1073/pnas.84.24.8951.
The Saccharomyces cerevisiae RAD3 gene, which is required for cell viability and excision repair of damaged DNA, encodes an 89-kDa protein that has a single-stranded DNA-dependent ATPase activity. We now show that the RAD3 protein also possesses a helicase activity that unwinds duplex regions in DNA substrates constructed by annealing DNA fragments of 71-851 nucleotides to circular, single-stranded M13 DNA. The DNA helicase activity is dependent on the hydrolysis of ATP, has a pH optimum of approximately 5.6, and is inhibited by antibodies raised against a truncated RAD3 protein produced in Escherichia coli. The RAD3 helicase translocates along single-stranded DNA in the 5'----3' direction. The direction of RAD3 helicase movement is consistent with the possibility that it unwinds DNA duplexes in advance of the replication fork during DNA replication.
酿酒酵母RAD3基因对细胞活力和受损DNA的切除修复是必需的,它编码一种89 kDa的蛋白质,该蛋白质具有单链DNA依赖性ATPase活性。我们现在表明,RAD3蛋白还具有解旋酶活性,可解开通过将71 - 851个核苷酸的DNA片段与环状单链M13 DNA退火构建的DNA底物中的双链区域。DNA解旋酶活性依赖于ATP的水解,最适pH约为5.6,并受到针对大肠杆菌中产生的截短RAD3蛋白产生的抗体的抑制。RAD3解旋酶沿单链DNA在5'----3'方向上移位。RAD3解旋酶的移动方向与它在DNA复制过程中在复制叉之前解开DNA双链的可能性一致。