Literature DB >> 10469666

Escherichia coli SeqA protein affects DNA topology and inhibits open complex formation at oriC.

N K Torheim1, K Skarstad.   

Abstract

Chromosome replication in Escherichia coli is initiated by the DnaA protein. Binding of DnaA to the origin, oriC, followed by formation of an open complex are the first steps in the initiation process. Based on in vivo studies the SeqA protein has been suggested to function negatively in the initiation of replication, possibly by inhibiting open complex formation. In vitro studies have shown that SeqA inhibits oriC-dependent replication. Here we show by KMnO(4) probing that SeqA inhibits open complex formation. The inhibition was not caused by prevention of DnaA binding to the oriC plasmids, indicating that SeqA prevented strand separation in oriC either directly, by interacting with the AT-rich region, or indirectly, by changing the topology of the oriC plasmids. SeqA was found to restrain the negative supercoils of the oriC plasmid. In comparison with the effect of HU on plasmid topology, SeqA seemed to act more cooperatively. It is likely that the inhibition of open complex formation is caused by the effect of SeqA on the topology of the plasmids. SeqA also restrained the negative supercoils of unmethylated oriC plasmids, which do not bind SeqA specifically, suggesting that the effect on topology is not dependent on binding of SeqA to a specific sequence in oriC.

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Year:  1999        PMID: 10469666      PMCID: PMC1171560          DOI: 10.1093/emboj/18.17.4882

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  23 in total

1.  The eclipse period of Escherichia coli.

Authors:  U von Freiesleben; M A Krekling; F G Hansen; A Løbner-Olesen
Journal:  EMBO J       Date:  2000-11-15       Impact factor: 11.598

2.  Supercoiling, knotting and replication fork reversal in partially replicated plasmids.

Authors:  L Olavarrieta; M L Martínez-Robles; J M Sogo; A Stasiak; P Hernández; D B Krimer; J B Schvartzman
Journal:  Nucleic Acids Res       Date:  2002-02-01       Impact factor: 16.971

3.  Degradation of mutant initiator protein DnaA204 by proteases ClpP, ClpQ and Lon is prevented when DNA is SeqA-free.

Authors:  Monika Slominska; Anne Wahl; Grzegorz Wegrzyn; Kirsten Skarstad
Journal:  Biochem J       Date:  2003-03-15       Impact factor: 3.857

4.  Structural and biochemical analyses of hemimethylated DNA binding by the SeqA protein.

Authors:  Norie Fujikawa; Hitoshi Kurumizaka; Osamu Nureki; Yoshinori Tanaka; Mitsuyoshi Yamazoe; Sota Hiraga; Shigeyuki Yokoyama
Journal:  Nucleic Acids Res       Date:  2004-01-02       Impact factor: 16.971

5.  Excess SeqA prolongs sequestration of oriC and delays nucleoid segregation and cell division.

Authors:  Trond Bach; Martin A Krekling; Kirsten Skarstad
Journal:  EMBO J       Date:  2003-01-15       Impact factor: 11.598

6.  Crystal structure of a SeqA-N filament: implications for DNA replication and chromosome organization.

Authors:  Alba Guarné; Therese Brendler; Qinghai Zhao; Rodolfo Ghirlando; Stuart Austin; Wei Yang
Journal:  EMBO J       Date:  2005-03-31       Impact factor: 11.598

7.  SeqA blocking of DnaA-oriC interactions ensures staged assembly of the E. coli pre-RC.

Authors:  Christian Nievera; Julien J-C Torgue; Julia E Grimwade; Alan C Leonard
Journal:  Mol Cell       Date:  2006-11-17       Impact factor: 17.970

Review 8.  Where does DNA replication start in archaea?

Authors:  A Vas; J Leatherwood
Journal:  Genome Biol       Date:  2000       Impact factor: 13.583

Review 9.  Regulating DNA replication in bacteria.

Authors:  Kirsten Skarstad; Tsutomu Katayama
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-04-01       Impact factor: 10.005

10.  Excess SeqA leads to replication arrest and a cell division defect in Vibrio cholerae.

Authors:  Djenann Saint-Dic; Jason Kehrl; Brian Frushour; Lyn Sue Kahng
Journal:  J Bacteriol       Date:  2008-07-11       Impact factor: 3.490

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