KOPS:: DNA motifs that control E-coli chromosome segregation by orienting the FtsK translocase

被引:154
作者
Bigot, S
Saleh, OA
Lesterlin, C
Pages, C
El Karoui, M
Dennis, C
Grigoriev, M
Allemand, JF
Barre, FX
Cornet, F
机构
[1] CNRS, LMGM, Toulouse, France
[2] ENS, LPS, F-75230 Paris, France
[3] INRA, URLGA, Jouy En Josas, France
[4] CNRS, LBME, Toulouse, France
[5] Dept Chim, Lab Pasteur, Paris, France
关键词
chromosome segregation; FtsK translocase; replichores;
D O I
10.1038/sj.emboj.7600835
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
Bacterial chromosomes are organized in replichores of opposite sequence polarity. This conserved feature suggests a role in chromosome dynamics. Indeed, sequence polarity controls resolution of chromosome dimers in Escherichia coli. Chromosome dimers form by homologous recombination between sister chromosomes. They are resolved by the combined action of two tyrosine recombinases, XerC and XerD, acting at a specific chromosomal site, dif, and a DNA translocase, FtsK, which is anchored at the division septum and sorts chromosomal DNA to daughter cells. Evidences suggest that DNA motifs oriented from the replication origin towards dif provide FtsK with the necessary information to faithfully distribute chromosomal DNA to either side of the septum, thereby bringing the dif sites together at the end of this process. However, the nature of the DNA motifs acting as FtsK orienting polar sequences (KOPS) was unknown. Using genetics, bioinformatics and biochemistry, we have identified a family of DNA motifs in the E. coli chromosome with KOPS activity.
引用
收藏
页码:3770 / 3780
页数:11
相关论文
共 39 条
[1]   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
[2]   FtsK activities in Xer recombination, DNA mobilization and cell division involve overlapping and separate domains of the protein [J].
Bigot, S ;
Corre, J ;
Louarn, JM ;
Cornet, F ;
Barre, FX .
MOLECULAR MICROBIOLOGY, 2004, 54 (04) :876-886
[3]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[4]   Estimating the persistence length of a worm-like chain molecule from force-extension measurements [J].
Bouchiat, C ;
Wang, MD ;
Allemand, JF ;
Strick, T ;
Block, SM ;
Croquette, V .
BIOPHYSICAL JOURNAL, 1999, 76 (01) :409-413
[5]   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
[6]   Restriction of the activity recombination site dif to a small zone of the Escherichia coli chromosome [J].
Cornet, F ;
Louarn, J ;
Patte, J ;
Louarn, JM .
GENES & DEVELOPMENT, 1996, 10 (09) :1152-1161
[7]   PLASMID PSC101 HARBORS A RECOMBINATION SITE, PSI, WHICH IS ABLE TO RESOLVE PLASMID MULTIMERS AND TO SUBSTITUTE FOR THE ANALOGOUS CHROMOSOMAL ESCHERICHIA-COLI SITE DIF [J].
CORNET, F ;
MORTIER, I ;
PATTE, J ;
LOUARN, JM .
JOURNAL OF BACTERIOLOGY, 1994, 176 (11) :3188-3195
[8]   Evidence from terminal recombination gradients that FtsK uses replichore polarity to control chromosome terminus positioning at division in Escherichia coli [J].
Corre, J ;
Louarn, JM .
JOURNAL OF BACTERIOLOGY, 2002, 184 (14) :3801-3807
[9]  
Corre J, 2000, GENETICS, V154, P39
[10]   ROLE OF THE ESCHERICHIA-COLI RECOMBINATION HOTSPOT, CHI, IN RECABCD-DEPENDENT HOMOLOGOUS PAIRING [J].
DIXON, DA ;
KOWALCZYKOWSKI, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (27) :16360-16370