SPECIFICITY OF BINDING TO 4-WAY JUNCTIONS IN DNA BY BACTERIOPHAGE-T7 ENDONUCLEASE-I

被引:40
作者
PARSONS, CA [1 ]
WEST, SC [1 ]
机构
[1] IMPERIAL CANC RES FUND, CLARE HALL LABS, S MIMMS EN6 3LD, HERTS, ENGLAND
关键词
D O I
10.1093/nar/18.15.4377
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
T7 endonuclease I binds specifically to four-way junctions in duplex DNA and promotes their resolution into linear duplexes. Under conditions in which the nuclease activity is blocked by the absence of divalent cations, the enzyme forms a distinct protein-DNA complex with the junction, as detected by gel retardation and filter binding assays. The formation of this complex is structure-specific and contrasts with the short-lived binding complexes formed on linear duplex DNA. The binding complex between T7 endonuclease I and a synthetic Holliday junction analog has been probed with hydroxyl radicals. The results indicate that the nuclease binds all four strands about the junction point. © 1990 Oxford University Press.
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页码:4377 / 4384
页数:8
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