Conserved sequence preference in DNA binding among recombination proteins: an effect of ssDNA secondary structure

被引:73
作者
Biet, E
Sun, JS
Dutreix, M
机构
[1] Inst Curie, Sect Rech, CNRS, UMR 144, F-75248 Paris 05, France
[2] Museum Natl Hist Nat, Biophys Lab, CNRS, URA481,INSERM,U201, F-75231 Paris, France
关键词
D O I
10.1093/nar/27.2.596
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
Repetitive sequences have been proposed to be recombinogenic elements in eukaryotic chromosomes, We tested whether dinucleotide repeats sequences are preferential sites for recombination because of their high affinity for recombination enzymes. We compared the kinetics of the binding of the scRad51, hsRad51 and ecRecA proteins to oligonucleotides with repeats of dinucleotides GT, CA, CT, GA, GC or AT, Since secondary structures in single-stranded DNA (ssDNA) act as a barrier to complete binding we measured whether these oligonucleotides are able to form stable secondary structures. We show that the preferential binding of recombination proteins is conserved among the three proteins and is influenced mainly by secondary structures in ssDNA.
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页码:596 / 600
页数:5
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