The Initiator Protein DnaA Contributes to Keeping New Origins Inactivated by Promoting the Presence of Hemimethylated DNA

被引:14
作者
Bach, Trond Morigen [1 ]
Skarstad, Kirsten [1 ]
机构
[1] Univ Oslo, Rigshosp, Norwegian Radium Hosp, Inst Canc Res,Dept Cell Biol, N-0310 Oslo, Norway
关键词
sequestration; hemimethylation; DnaA; SeqA; oriC;
D O I
10.1016/j.jmb.2008.09.042
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
The Escherichia coli replication origin oriC and other regions with high numbers of GATC sites remain hemimethylated after replication much longer than regions with average numbers of GATC sites. The prolonged period of hemimethylation has been attributed to the presence of bound SeqA protein. Here, it was found that a GATC cluster inserted at the datA site, which binds large amounts of DnaA in vivo, did not become remethylated at all, unless the availability of the DnaA protein was severely reduced. Sequestration of oriC was also found to be affected by the availability of DnaA. The period of origin hemimethylation was reduced by similar to 30% upon a reduction in the availability of DnaA. The result shows that not only SeqA binding but also DnaA binding to newly replicated origins contributes to keeping them hemimethylated. It was also found that the number of SeqA foci increased in cells with a combination of DnaA-mediated protection and sequestration at the GATC: :datA cluster. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1076 / 1085
页数:10
相关论文
共 51 条
[1]   An oriC-like distribution of GATC sites mediates full sequestration of non-origin sequences in Escherichia coli [J].
Bach, T ;
Skarstad, K .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 350 (01) :7-11
[2]   Re-replication from non-sequesterable origins generates three-nucleoid cells which divide asymmetrically [J].
Bach, T ;
Skarstad, K .
MOLECULAR MICROBIOLOGY, 2004, 51 (06) :1589-1600
[3]   Excess SeqA prolongs sequestration of oriC and delays nucleoid segregation and cell division [J].
Bach, T ;
Krekling, MA ;
Skarstad, K .
EMBO JOURNAL, 2003, 22 (02) :315-323
[4]  
BOYE E, 1992, REGULATION DNA REPLI
[5]   A case for sliding SeqA tracts at anchored replication forks during Escherichia coli chromosome replication and segregation [J].
Brendler, T ;
Sawitzke, J ;
Sergueev, K ;
Austin, S .
EMBO JOURNAL, 2000, 19 (22) :6249-6258
[6]   ESCHERICHIA-COLI ORIC AND THE DNAA GENE PROMOTER ARE SEQUESTERED FROM DAM METHYLTRANSFERASE FOLLOWING THE PASSAGE OF THE CHROMOSOMAL REPLICATION FORK [J].
CAMPBELL, JL ;
KLECKNER, N .
CELL, 1990, 62 (05) :967-979
[7]   CELL CYCLE-SPECIFIC CHANGES IN NUCLEOPROTEIN COMPLEXES AT A CHROMOSOMAL REPLICATION ORIGIN [J].
CASSLER, MR ;
GRIMWADE, JE ;
LEONARD, AC .
EMBO JOURNAL, 1995, 14 (23) :5833-5841
[8]   CONSTRUCTION AND CHARACTERIZATION OF AMPLIFIABLE MULTICOPY DNA CLONING VEHICLES DERIVED FROM P15A CRYPTIC MINIPLASMID [J].
CHANG, ACY ;
COHEN, SN .
JOURNAL OF BACTERIOLOGY, 1978, 134 (03) :1141-1156
[9]   Escherichia coli DnaA interacts with HU in initiation at the E-coli replication origin [J].
Chodavarapu, Sundarl ;
Felczak, Magdalena M. ;
Rouviere-Yaniv, Josette ;
Kaguni, Jon M. .
MOLECULAR MICROBIOLOGY, 2008, 67 (04) :781-792
[10]   DNA REPLICATION AND DIVISION CYCLE IN ESCHERICHIA COLI [J].
CLARK, DJ ;
MAALOE, O .
JOURNAL OF MOLECULAR BIOLOGY, 1967, 23 (01) :99-&