BIOCHEMICAL INTERACTION OF THE ESCHERICHIA-COLI RECF, RECO, AND RECR PROTEINS WITH RECA PROTEIN AND SINGLE-STRANDED-DNA BINDING-PROTEIN

被引:221
作者
UMEZU, K
CHI, NW
KOLODNER, RD
机构
[1] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV CELL & MOLEC BIOL,44 BINNEY ST,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,DEPT BIOL CHEM & MOLEC PHARMACOL,BOSTON,MA 02115
关键词
GENETIC RECOMBINATION; RECF PATHWAY; STRAND TRANSFER; DNA REPAIR;
D O I
10.1073/pnas.90.9.3875
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Escherichia coli RecF, RecO, and RecR proteins were analyzed for their effect on RecA-mediated pairing of single-stranded circular DNA and homologous linear duplex DNA substrates. As shown by other workers, joint molecule formation by RecA was inhibited by E. coli single-stranded DNA binding protein (SSB) when it was added to single-stranded DNA before RecA. This inhibitory effect was overcome by the addition of RecO and RecR or RecF, RecO, and RecR. Both the rate and extent of joint molecule formation were restored to the maximal level observed when SSB was added after RecA. RecF, RecO, and RecR proteins had no effect on the conversion of joint molecules to final products and only appeared to stimulate an early step in the pairing reaction. The stimulatory effect of RecF, RecO, and RecR was not seen without SSB or when SSB was added after RecA. RecF protein by itself inhibited reactions in mixtures containing RecA and SSB, and this inhibition was overcome by the addition of RecO and RecR. These data suggest that RecO and RecR, and possibly RecF, help RecA overcome inhibition by SSB and utilize SSB-single-stranded-DNA complexes as substrates.
引用
收藏
页码:3875 / 3879
页数:5
相关论文
共 36 条
[1]  
AKEEL AM, 1989, MOL GEN GENET, V216, P503
[2]  
BROSIUS J, 1984, P NATL ACAD SCI USA, V81, P6292
[3]   REC GENES AND HOMOLOGOUS RECOMBINATION PROTEINS IN ESCHERICHIA-COLI [J].
CLARK, AJ .
BIOCHIMIE, 1991, 73 (04) :523-532
[4]   RESOLUTION OF HOLLIDAY JUNCTIONS INVITRO REQUIRES THE ESCHERICHIA-COLI RUVC GENE-PRODUCT [J].
CONNOLLY, B ;
PARSONS, CA ;
BENSON, FE ;
DUNDERDALE, HJ ;
SHARPLES, GJ ;
LLOYD, RG ;
WEST, SC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (14) :6063-6067
[5]  
COX MM, 1982, J BIOL CHEM, V257, P8523
[6]   ENZYMES OF GENERAL RECOMBINATION [J].
COX, MM ;
LEHMAN, IR .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :229-262
[7]  
GRIFFIN TJ, 1990, J BACTERIOL, V172, P6921
[8]   RECA PROTEIN RAPIDLY CRYSTALLIZES IN THE PRESENCE OF SPERMIDINE - A VALUABLE STEP IN ITS PURIFICATION AND PHYSICAL CHARACTERIZATION [J].
GRIFFITH, J ;
SHORES, CG .
BIOCHEMISTRY, 1985, 24 (01) :158-162
[9]   GENETIC ANALYSIS OF RECF PATHWAY TO GENETIC RECOMBINATION IN ESCHERICHIA-COLI K12 - ISOLATION AND CHARACTERIZATION OF MUTANTS [J].
HORII, ZI ;
CLARK, AJ .
JOURNAL OF MOLECULAR BIOLOGY, 1973, 80 (02) :327-&
[10]   ESCHERICHIA-COLI RUVC PROTEIN IS AN ENDONUCLEASE THAT RESOLVES THE HOLLIDAY STRUCTURE [J].
IWASAKI, H ;
TAKAHAGI, M ;
SHIBA, T ;
NAKATA, A ;
SHINAGAWA, H .
EMBO JOURNAL, 1991, 10 (13) :4381-4389