Species specificity in the activation of Xer recombination at dif by FtsK

被引:41
作者
Yates, J
Aroyo, M
Sherratt, DJ
Barre, FX
机构
[1] Univ Oxford, Dept Biochem, Div Mol Genet, Oxford OX1 3QU, England
[2] CNRS, Lab Microbiol & Genet Mol, UMR 5100, F-31062 Toulouse, France
关键词
D O I
10.1046/j.1365-2958.2003.03574.x
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
In Escherichia coli , chromosome dimers are resolved to monomers by the addition of a single cross-over at a specific locus on the chromosome, dif . Recombination is performed by two tyrosine recombinases, XerC and XerD, and requires the action of an additional protein, FtsK. We show that Haemophilus influenzae FtsK activates recombination by H. influenzae XerCD at H. influenzae dif . However, it cannot activate recombination by E. coli XerCD. Reciprocally, E. coli FtsK cannot activate recombination by the H. influenzae recombinases at H. influenzae dif . We took advantage of this species specificity to gain further insight into the mechanism of activation of Xer recombination at dif by FtsK. We mapped the region of FtsK implicated in species specificity to the extreme 140-amino-acid C-terminal residues of the protein. Our results suggest that FtsK interacts directly with XerCD in order to activate recombination at dif .
引用
收藏
页码:241 / 249
页数:9
相关论文
共 39 条
[1]   Coordinated control of XerC and XerD catalytic activities during Holliday junction resolution [J].
Arciszewska, LK ;
Baker, RA ;
Hallet, B ;
Sherratt, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 299 (02) :391-403
[2]   XER SITE-SPECIFIC RECOMBINATION IN-VITRO [J].
ARCISZEWSKA, LK ;
SHERRATT, DJ .
EMBO JOURNAL, 1995, 14 (09) :2112-2120
[3]   FtsK is a DNA motor protein that activates chromosome dimer resolution by switching the catalytic state of the XerC and XerD recombinases [J].
Aussel, L ;
Barre, FX ;
Aroyo, M ;
Stasiak, A ;
Stasiak, AZ ;
Sherratt, D .
CELL, 2002, 108 (02) :195-205
[4]  
Barre F.X., 2002, MOBILE DNA-UK, P149
[5]   FtsK functions in the processing of a Holliday junction intermediate during bacterial chromosome segregation [J].
Barre, FX ;
Aroyo, M ;
Colloms, SD ;
Helfrich, A ;
Cornet, F ;
Sherratt, DJ .
GENES & DEVELOPMENT, 2000, 14 (23) :2976-2988
[6]   Circles: The replication-recombination-chromosome segregation connection [J].
Barre, FX ;
Soballe, B ;
Michel, B ;
Aroyo, M ;
Robertson, M ;
Sherratt, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8189-8195
[7]  
BLAKELY G, 1991, NEW BIOL, V3, P789
[8]   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
[9]   A dual role for the FtsK protein in Escherichia coli chromosome segregation [J].
Capiaux, H ;
Lesterlin, C ;
Pérals, K ;
Louarn, JM ;
Cornet, F .
EMBO REPORTS, 2002, 3 (06) :532-536
[10]   FtsQ, FtsL and FtsI require FtsK, but not FtsN, for co-localization with FtsZ during Escherichia coli cell division [J].
Chen, JC ;
Beckwith, J .
MOLECULAR MICROBIOLOGY, 2001, 42 (02) :395-413