Site-specific cleavage of DNA-RNA hybrids by zinc finger FokI cleavage domain fusions

被引:62
作者
Kim, YG
Shi, YG
Berg, JM
Chandrasegaran, S
机构
[1] Johns Hopkins Univ, Sch Hyg & Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Biophys & Biophys Chem, Baltimore, MD 21205 USA
关键词
Flavorbacterium okeanokoites; chimeric restriction endonuclease; protein engineering; recognition and cleavage domains;
D O I
10.1016/S0378-1119(97)00489-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Zinc-finger proteins of the Cys(2)His(2) type bind DNA-RNA hybrids with affinities comparable to those for DNA duplexes. Such zinc-finger proteins were converted into site-specific cleaving enzymes by fusing them to the FokI cleavage domain. The fusion proteins are active and under optimal conditions cleave DNA duplexes in a sequence-specific manner. These fusions also exhibit site-specific cleavage of the DNA strand within DNA-RNA hybrids albeit at a lower efficiency (similar or equal to 50-fold) compared to the cleavage of the DNA duplexes. These engineered endonucleases represent the first of their kind in terms of their DNA-RNA cleavage properties, and they may have important biological applications. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:43 / 49
页数:7
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