Alleva J L, Doetsch P W
Department of Biochemistry, Graduate Program in Genetics and Molecular Biology and Division of Cancer Biology, Department of Radiation Oncology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Nucleic Acids Res. 2000 Aug 1;28(15):2893-901. doi: 10.1093/nar/28.15.2893.
The nuclease activity of FEN-1 is essential for both DNA replication and repair. Intermediate DNA products formed during these processes possess a variety of structures and termini. We have previously demonstrated that the 5'-->3' exonuclease activity of the Schizosaccharomyces pombe FEN-1 protein Rad2p requires a 5'-phosphoryl moiety to efficiently degrade a nick-containing substrate in a reconstituted alternative excision repair system. Here we report the effect of different 5'-terminal moieties of a variety of DNA substrates on Rad2p activity. We also show that Rad2p possesses a 5'-->3' single-stranded exonuclease activity, similar to Saccharomyces cerevisiae Rad27p and phage T5 5'-->3' exonuclease (also a FEN-1 homolog). FEN-1 nucleases have been associated with the base excision repair pathway, specifically processing cleaved abasic sites. Because several enzymes cleave abasic sites through different mechanisms resulting in different 5'-termini, we investigated the ability of Rad2p to process several different types of cleaved abasic sites. With varying efficiency, Rad2p degrades the products of an abasic site cleaved by Escherichia coli endonuclease III and endonuclease IV (prototype AP endonucleases) and S.POMBE: Uve1p. These results provide important insights into the roles of Rad2p in DNA repair processes in S.POMBE:
FEN-1的核酸酶活性对于DNA复制和修复均至关重要。在这些过程中形成的中间DNA产物具有多种结构和末端。我们之前已经证明,裂殖酵母FEN-1蛋白Rad2p的5'→3'核酸外切酶活性需要一个5'-磷酸基团,才能在重组的替代切除修复系统中有效降解含切口的底物。在此我们报告了多种DNA底物的不同5'-末端基团对Rad2p活性的影响。我们还表明,Rad2p具有5'→3'单链核酸外切酶活性,类似于酿酒酵母Rad27p和噬菌体T5 5'→3'核酸外切酶(也是一种FEN-1同源物)。FEN-1核酸酶与碱基切除修复途径相关,特别是处理切割后的无碱基位点。由于几种酶通过不同机制切割无碱基位点,产生不同的5'-末端,我们研究了Rad2p处理几种不同类型切割后无碱基位点的能力。Rad2p以不同效率降解由大肠杆菌核酸内切酶III和核酸内切酶IV(典型的AP核酸内切酶)以及粟酒裂殖酵母Uve1p切割产生的无碱基位点产物。这些结果为Rad2p在粟酒裂殖酵母DNA修复过程中的作用提供了重要见解。