Mutations altering the cleavage specificity of a homing endonuclease

被引:84
作者
Seligman, LM
Chevalier, BS
Chadsey, MS
Edwards, ST
Savage, JH
Veillet, AL
机构
[1] Pomona Coll, Dept Biol, Claremont, CA 91711 USA
[2] Pomona Coll, Program Mol Biol, Claremont, CA 91711 USA
[3] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[4] Univ Washington, Grad Program Mol & Cell Biol, Seattle, WA 98109 USA
[5] Univ Washington, Dept Pathol & Genome Sci, Seattle, WA 98195 USA
关键词
D O I
10.1093/nar/gkf495
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
The homing endonuclease I-CreI recognizes and cleaves a particular 22 bp DNA sequence. The crystal structure of I-CreI bound to homing site DNA has previously been determined, leading to a number of predictions about specific protein-DNA contacts. We test these predictions by analyzing a set of endonuclease mutants and a complementary set of homing site mutants. We find evidence that all structurally predicted I-CreI/DNA contacts contribute to DNA recognition and show that these contacts differ greatly in terms of their relative importance. We also describe the isolation of a collection of altered specificity I-CreI derivatives. The in vitro DNA-binding and cleavage properties of two such endonucleases demonstrate that our genetic approach is effective in identifying homing endonucleases that recognize and cleave novel target sequences.
引用
收藏
页码:3870 / 3879
页数:10
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