Literature DB >> 8808623

Replisome assembly reveals the basis for asymmetric function in leading and lagging strand replication.

A Yuzhakov1, J Turner, M O'Donnell.   

Abstract

The E. coli replicase, DNA polymerase III holoenzyme, contains two polymerases for replication of duplex DNA. The DNA strands are antiparallel requiring different modes of replicating the two strands: one is continuous (leading) while the other is discontinuous (lagging). The two polymerases within holoenzyme are generally thought to have asymmetric functions for replication of these two strands. This report finds that the two polymerases have equal properties, both are capable of replicating the more difficult lagging strand. Asymmetric action is, however, imposed by the helicase that encircles the lagging strand. The helicase contact defines the leading polymerase constraining it to a subset of actions, while leaving the other to cycle on the lagging strand. The symmetric actions of the two polymerases free holoenzyme to assemble into the replisome in either orientation without concern for a correct match to one or the other strand.

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Year:  1996        PMID: 8808623     DOI: 10.1016/s0092-8674(00)80163-4

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  48 in total

Review 1.  Role of PriA in replication fork reactivation in Escherichia coli.

Authors:  S J Sandler; K J Marians
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

2.  Escherichia coli DNA polymerase III tau- and gamma-subunit conserved residues required for activity in vivo and in vitro.

Authors:  J R Walker; C Hervas; J D Ross; A Blinkova; M J Walbridge; E J Pumarega; M O Park; H R Neely
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

3.  Mechanism of termination of DNA replication of Escherichia coli involves helicase-contrahelicase interaction.

Authors:  S Mulugu; A Potnis; J Taylor; K Alexander; D Bastia
Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-07       Impact factor: 11.205

4.  The DnaC helicase loader is a dual ATP/ADP switch protein.

Authors:  Megan J Davey; Linhua Fang; Peter McInerney; Roxana E Georgescu; Mike O'Donnell
Journal:  EMBO J       Date:  2002-06-17       Impact factor: 11.598

5.  A peptide switch regulates DNA polymerase processivity.

Authors:  Francisco J López de Saro; Roxana E Georgescu; Mike O'Donnell
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-20       Impact factor: 11.205

6.  Protein trafficking on sliding clamps.

Authors:  Francisco López de Saro; Roxana E Georgescu; Frank Leu; Mike O'Donnell
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2004-01-29       Impact factor: 6.237

Review 7.  Mechanisms of replication fork restart in Escherichia coli.

Authors:  Kenneth J Marians
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2004-01-29       Impact factor: 6.237

8.  DnaB helicase activity is modulated by DNA geometry and force.

Authors:  Noah Ribeck; Daniel L Kaplan; Irina Bruck; Omar A Saleh
Journal:  Biophys J       Date:  2010-10-06       Impact factor: 4.033

9.  Conservation of the Escherichia coli dnaX programmed ribosomal frameshift signal in Salmonella typhimurium.

Authors:  A Blinkova; M F Burkart; T D Owens; J R Walker
Journal:  J Bacteriol       Date:  1997-07       Impact factor: 3.490

10.  Mrc1 and Tof1 regulate DNA replication forks in different ways during normal S phase.

Authors:  Ben Hodgson; Arturo Calzada; Karim Labib
Journal:  Mol Biol Cell       Date:  2007-07-25       Impact factor: 4.138

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