Literature DB >> 7929435

Tus prevents overreplication of oriC plasmid DNA.

H Hiasa1, K J Marians.   

Abstract

Minichromosome plasmid DNA templates containing oriC and two Ter sites, oriented as they are on the Escherichia coli chromosome, have been used to study the role of Tus in termination of bidirectional replication. In replication reactions reconstituted with purified proteins where it could be demonstrated that each active template was replicating bidirectionally, Tus was required to prevent extensive overreplication. In the presence of Tus, both replication forks terminated DNA synthesis at one or the other Ter site in an apparent stepwise manner. First, the progress of one replication fork was arrested by a properly oriented Tus-Ter complex. Then, either because of steric hindrance resulting from the stalled replication machinery of the first fork or because of the formation of a branched DNA structure, the progression of the second opposing fork was halted at the same site on the DNA template. In the absence of Tus, overreplication required DNA ligase and arose via a template strand-switching mechanism. Thus, the role of Tus in E. coli is more likely to prevent overreplication rather than to ensure accurate termination.

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Year:  1994        PMID: 7929435

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  32 in total

1.  RecG protein and single-strand DNA exonucleases avoid cell lethality associated with PriA helicase activity in Escherichia coli.

Authors:  Christian J Rudolph; Akeel A Mahdi; Amy L Upton; Robert G Lloyd
Journal:  Genetics       Date:  2010-07-20       Impact factor: 4.562

Review 2.  Replication termination in Escherichia coli: structure and antihelicase activity of the Tus-Ter complex.

Authors:  Cameron Neylon; Andrew V Kralicek; Thomas M Hill; Nicholas E Dixon
Journal:  Microbiol Mol Biol Rev       Date:  2005-09       Impact factor: 11.056

Review 3.  Replication fork stalling at natural impediments.

Authors:  Ekaterina V Mirkin; Sergei M Mirkin
Journal:  Microbiol Mol Biol Rev       Date:  2007-03       Impact factor: 11.056

4.  Resolution of converging replication forks by RecQ and topoisomerase III.

Authors:  Catherine Suski; Kenneth J Marians
Journal:  Mol Cell       Date:  2008-06-20       Impact factor: 17.970

Review 5.  RecBCD is required to complete chromosomal replication: Implications for double-strand break frequencies and repair mechanisms.

Authors:  Justin Courcelle; Brian M Wendel; Dena D Livingstone; Charmain T Courcelle
Journal:  DNA Repair (Amst)       Date:  2015-05-02

6.  Two mechanisms coordinate replication termination by the Escherichia coli Tus-Ter complex.

Authors:  Manjula Pandey; Mohamed M Elshenawy; Slobodan Jergic; Masateru Takahashi; Nicholas E Dixon; Samir M Hamdan; Smita S Patel
Journal:  Nucleic Acids Res       Date:  2015-05-24       Impact factor: 16.971

7.  Completion of DNA replication in Escherichia coli.

Authors:  Brian M Wendel; Charmain T Courcelle; Justin Courcelle
Journal:  Proc Natl Acad Sci U S A       Date:  2014-11-03       Impact factor: 11.205

8.  Experimental identification and characterization of 97 novel npcRNA candidates in Salmonella enterica serovar Typhi.

Authors:  Suresh V Chinni; Carsten A Raabe; Robaiza Zakaria; Gerrit Randau; Chee Hock Hoe; Anja Zemann; Juergen Brosius; Thean-Hock Tang; Timofey S Rozhdestvensky
Journal:  Nucleic Acids Res       Date:  2010-05-11       Impact factor: 16.971

9.  Pathological replication in cells lacking RecG DNA translocase.

Authors:  Christian J Rudolph; Amy L Upton; Lynda Harris; Robert G Lloyd
Journal:  Mol Microbiol       Date:  2009-06-16       Impact factor: 3.501

10.  Replication fork collisions cause pathological chromosomal amplification in cells lacking RecG DNA translocase.

Authors:  Christian J Rudolph; Amy L Upton; Robert G Lloyd
Journal:  Mol Microbiol       Date:  2009-10-08       Impact factor: 3.501

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