FUNCTIONAL DOMAINS WITHIN FEN-1 AND RAD2 DEFINE A FAMILY OF STRUCTURE-SPECIFIC ENDONUCLEASES - IMPLICATIONS FOR NUCLEOTIDE EXCISION-REPAIR

被引:277
作者
HARRINGTON, JJ [1 ]
LIEBER, MR [1 ]
机构
[1] STANFORD UNIV,SCH MED,DEPT PATHOL,EXPTL ONCOL LAB,STANFORD,CA 94305
关键词
FEN-1; RAD2; YKL510; NUCLEASE; NUCLEOTIDE EXCISION REPAIR; STRUCTURE SPECIFIC;
D O I
10.1101/gad.8.11.1344
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Structure-specific nucleases catalyze critical reactions in DNA replication, recombination, and repair. Recently, a structure-specific endonuclease, FEN-1, has been purified and shown to cleave DNA flap structures. Here, we describe the cloning of the murine FEN-1 gene. The nucleotide sequence of FEN-1 is highly homologous to the Saccharomyces cerevisiae genes YKL510 and RAD2. We show that YKLS10 and a truncated RAD2 protein are also structure-specific endonucleases. The substrate specificity of the truncated RAD2 protein implicates branched DNA structures as important intermediates in nucleotide excision repair. The polarity of these branched DNA structures allows us to predict the placement of DNA scissions by RAD2 and RAD1/RAD10 in this reaction.
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页码:1344 / 1355
页数:12
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