Direct interaction of aminopeptidase A with recombination site DNA in Xer site-specific recombination

被引:61
作者
Alen, C [1 ]
Sherratt, DJ [1 ]
Colloms, SD [1 ]
机构
[1] UNIV OXFORD,DEPT BIOCHEM,MICROBIOL UNIT,OXFORD OX1 3QU,ENGLAND
基金
英国惠康基金;
关键词
ArgR; cer; PepA; site-specific recombination; Xer;
D O I
10.1093/emboj/16.17.5188
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
Xer site-specific recombination at ColE1 cer converts plasmid multimers into monomers, thus ensuring the heritable stability of ColE1, Two related recombinase proteins, XerC and XerD, catalyse the strand exchange reaction at a 30 bp recombination core site, In addition, two accessory proteins, PepA and ArgR, are required for recombination at cer. These two accessory proteins are thought to act at 180 bp of accessory sequences adjacent to the cer recombination core to ensure that recombination only occurs between directly repeated sites on the same molecule, Here, we demonstrate that PepA and ArgR interact directly with cer, forming a complex in which the accessory sequences of two cer sites are interwrapped approximately three times in a right-handed fashion, We present a model for this synaptic complex, and propose that strand exchange can only occur after the formation of this complex.
引用
收藏
页码:5188 / 5197
页数:10
相关论文
共 26 条
[1]   LEUCINE AMINOPEPTIDASE FROM ARABIDOPSIS-THALIANA - MOLECULAR EVIDENCE FOR A PHYLOGENETICALLY CONSERVED ENZYME OF PROTEIN-TURNOVER IN HIGHER-PLANTS [J].
BARTLING, D ;
WEILER, EW .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 205 (01) :425-431
[2]   2 RELATED RECOMBINASES ARE REQUIRED FOR SITE-SPECIFIC RECOMBINATION AT DIF AND CER IN ESCHERICHIA-COLI K12 [J].
BLAKELY, G ;
MAY, G ;
MCCULLOCH, R ;
ARCISZEWSKA, LK ;
BURKE, M ;
LOVETT, ST ;
SHERRATT, DJ .
CELL, 1993, 75 (02) :351-361
[3]   MUTANT ESCHERICHIA-COLI ARGININE REPRESSOR PROTEINS THAT FAIL TO BIND L-ARGININE, YET RETAIN THE ABILITY TO BIND THEIR NORMAL DNA-BINDING SITES [J].
BURKE, M ;
MERICAN, AF ;
SHERRATT, DJ .
MOLECULAR MICROBIOLOGY, 1994, 13 (04) :609-618
[4]   STRUCTURE DETERMINATION AND REFINEMENT OF BOVINE LENS LEUCINE AMINOPEPTIDASE AND ITS COMPLEX WITH BESTATIN [J].
BURLEY, SK ;
DAVID, PR ;
SWEET, RM ;
TAYLOR, A ;
LIPSCOMB, WN .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 224 (01) :113-140
[5]   CARP, INVOLVED IN PYRIMIDINE REGULATION OF THE ESCHERICHIA-COLI CARBAMOYLPHOSPHATE SYNTHETASE OPERON ENCODES A SEQUENCE-SPECIFIC DNA-BINDING PROTEIN IDENTICAL TO XERB AND PEPA, ALSO REQUIRED FOR RESOLUTION OF COLEI MULTIMERS [J].
CHARLIER, D ;
HASSANZADEH, G ;
KHOLTI, A ;
GIGOT, D ;
PIERARD, A ;
GLANSDORFF, N .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 250 (04) :392-406
[6]   Topological selectivity in Xer site-specific recombination [J].
Colloms, SD ;
Bath, J ;
Sherratt, DJ .
CELL, 1997, 88 (06) :855-864
[7]   RECOMBINATION AT COLE1 CER REQUIRES THE ESCHERICHIA-COLI XERC GENE-PRODUCT, A MEMBER OF THE LAMBDA-INTEGRASE FAMILY OF SITE-SPECIFIC RECOMBINASES [J].
COLLOMS, SD ;
SYKORA, P ;
SZATMARI, G ;
SHERRATT, DJ .
JOURNAL OF BACTERIOLOGY, 1990, 172 (12) :6973-6980
[8]  
COLLOMS SD, 1996, EMBO J, V15, P1171
[9]   PROCESSIVE RECOMBINATION BY WILD-TYPE GIN AND AN ENHANCER-INDEPENDENT MUTANT - INSIGHT INTO THE MECHANISMS OF RECOMBINATION SELECTIVITY AND STRAND EXCHANGE [J].
CRISONA, NJ ;
KANAAR, R ;
GONZALEZ, TN ;
ZECHIEDRICH, EL ;
KLIPPEL, A ;
COZZARELLI, NR .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 243 (03) :437-457
[10]  
CUYPERS HT, 1982, J BIOL CHEM, V257, P7077