Effect of deletion mutation on the recombination activity of Cre recombinase.
Author(s) -
Rongrong Liu,
Lixia Wang,
Zhongping Lin
Publication year - 2005
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2005_3470
Subject(s) - recombinase , mutant , recombination , cre recombinase , flp frt recombination , escherichia coli , genetics , biology , site specific recombination , bacteriophage , dna , mutation , microbiology and biotechnology , cre lox recombination , tn3 transposon , genetic recombination , gene , transgene , transposable element , genetically modified mouse
Cre recombinase from bacteriophage P1 is widely used in both in vitro and in vivo DNA manipulations. Based on a structural and functional analysis, three deleted cre mutants were constructed and expressed in Escherichia coli. Mutated recombinases were purified and their recombination activities were determined in vitro. Our results revealed that the mutant with amino-terminal deletion retains the recombination activity as high as wild type Cre; however, the carboxy-terminal deletion and the middle region deletion both lead to a complete loss of the recombinase function.
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