Literature DB >> 2525129

Ordered assembly of nucleoprotein structures at the bacteriophage lambda replication origin during the initiation of DNA replication.

C Alfano1, R McMacken.   

Abstract

Replication of the chromosome of bacteriophage lambda depends on the cooperative action of two phage-coded proteins and seven replication and heat shock proteins from its Escherichia coli host. As previously described, the first stage in this process is the binding of multiple copies of the lambda O initiator to the lambda replication origin (ori lambda) to form the nucleosomelike O-some. The O-some serves to localize subsequent protein-protein and protein-DNA interactions involved in the initiation of lambda DNA replication to ori lambda. To study these interactions, we have developed a sensitive immunoblotting protocol that permits the protein constituents of complex nucleoprotein structures to be identified. Using this approach, we have defined a series of sequential protein assembly and protein disassembly events that occur at ori lambda during the initiation of lambda DNA replication. A second-stage ori lambda.O (lambda O protein).P (lambda P protein).DnaB nucleoprotein structure is formed when O, P, and E. coli DnaB helicase are incubated with ori lambda DNA. In a third-stage reaction the E. coli DnaJ heat shock protein specifically binds to the second-stage structure to form an ori lambda.O.P.DnaB.DnaJ complex. Each of the nucleoprotein structures formed in the first three stages was isolated and shown to be a physiological intermediate in the initiation of lambda DNA replication. The E. coli DnaK heat shock protein can bind to any of these early stage nucleoprotein structures, and in a fourth-stage reaction a complete ori lambda.O.P.DnaB.DnaJ.DnaK initiation complex is assembled. Addition of ATP to the reaction enables the DnaK and DnaJ heat shock proteins to mediate a partial disassembly of the fourth-stage complex. These protein disassembly reactions activate the intrinsic helicase activity of DnaB and result in localized unwinding of the ori lambda template. The protein disassembly reactions are described in the accompanying articles.

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Year:  1989        PMID: 2525129

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


  51 in total

1.  Partial loss of function mutations in DnaK, the Escherichia coli homologue of the 70-kDa heat shock proteins, affect highly conserved amino acids implicated in ATP binding and hydrolysis.

Authors:  J Wild; A Kamath-Loeb; E Ziegelhoffer; M Lonetto; Y Kawasaki; C A Gross
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-01       Impact factor: 11.205

Review 2.  Two heads are better than one: regulation of DNA replication by hexameric helicases.

Authors:  Robert A Sclafani; Ryan J Fletcher; Xiaojiang S Chen
Journal:  Genes Dev       Date:  2004-09-01       Impact factor: 11.361

3.  Crystallization and preliminary crystallographic characterization of the origin-binding domain of the bacteriophage lambda O replication initiator.

Authors:  E B Struble; A G Gittis; M A Bianchet; R McMacken
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2007-05-31

Review 4.  Cell cycle regulation of DNA replication.

Authors:  R A Sclafani; T M Holzen
Journal:  Annu Rev Genet       Date:  2007       Impact factor: 16.830

5.  Formation of the preprimosome protects lambda O from RNA transcription-dependent proteolysis by ClpP/ClpX.

Authors:  M Zylicz; K Liberek; A Wawrzynow; C Georgopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

6.  ClpX protein of Escherichia coli activates bacteriophage Mu transposase in the strand transfer complex for initiation of Mu DNA synthesis.

Authors:  R Kruklitis; D J Welty; H Nakai
Journal:  EMBO J       Date:  1996-02-15       Impact factor: 11.598

7.  Cryptic single-stranded-DNA binding activities of the phage lambda P and Escherichia coli DnaC replication initiation proteins facilitate the transfer of E. coli DnaB helicase onto DNA.

Authors:  B A Learn; S J Um; L Huang; R McMacken
Journal:  Proc Natl Acad Sci U S A       Date:  1997-02-18       Impact factor: 11.205

8.  Involvement of the DnaK-DnaJ-GrpE chaperone team in protein secretion in Escherichia coli.

Authors:  J Wild; P Rossmeissl; W A Walter; C A Gross
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

9.  Genetic interactions between KAR2 and SEC63, encoding eukaryotic homologues of DnaK and DnaJ in the endoplasmic reticulum.

Authors:  M A Scidmore; H H Okamura; M D Rose
Journal:  Mol Biol Cell       Date:  1993-11       Impact factor: 4.138

10.  DnaK mutants defective in ATPase activity are defective in negative regulation of the heat shock response: expression of mutant DnaK proteins results in filamentation.

Authors:  J S McCarty; G C Walker
Journal:  J Bacteriol       Date:  1994-02       Impact factor: 3.490

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