Literature DB >> 7806533

Purification and characterization of bacteriophage T4 gene 59 protein. A DNA helicase assembly protein involved in DNA replication.

J Barry1, B Alberts.   

Abstract

The T4 bacteriophage gene 59 protein is required for normal T4 DNA replication. We have purified this protein to homogeneity in two steps and show that it binds both to single-stranded DNA and to the T4 gene 32 protein, a DNA single strand binding protein. In in vitro assays, covering DNA with 32 protein makes this DNA inaccessible to the 41 protein, the highly processive DNA helicase, that associates with the T4 DNA primase (gene 61 protein) to form an active primosome. However, the 59 protein brings about the rapid assembly of 41 protein onto single-stranded DNA, even if this DNA is covered with 32 protein. The 59 protein is therefore a DNA helicase assembly protein. The observed requirements for the 59 protein in the vivo T4 DNA replication are explained by there being two alternative pathways for loading the 41 protein onto a replication fork at early times of T4 DNA synthesis, with only a 59 protein-mediated pathway remaining operative for the recombination-mediated replication that dominates later in infection (Barry, J., and Alberts, B. M. (1994) J. Biol. Chem. 269, 33063-33068).

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7806533

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


  25 in total

Review 1.  Mediator proteins orchestrate enzyme-ssDNA assembly during T4 recombination-dependent DNA replication and repair.

Authors:  J S Bleuit; H Xu; Y Ma; T Wang; J Liu; S W Morrical
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

Review 2.  Bacteriophage T4 gene 41 helicase and gene 59 helicase-loading protein: a versatile couple with roles in replication and recombination.

Authors:  C E Jones; T C Mueser; K C Dudas; K N Kreuzer; N G Nossal
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

3.  Characterization of DNA synthesis catalyzed by bacteriophage T4 replication complexes reconstituted on synthetic circular substrates.

Authors:  Farid A Kadyrov; John W Drake
Journal:  Nucleic Acids Res       Date:  2002-10-15       Impact factor: 16.971

4.  Mutational analysis of the T4 gp59 helicase loader reveals its sites for interaction with helicase, single-stranded binding protein, and DNA.

Authors:  Darin Dolezal; Charles E Jones; Xiaoqin Lai; J Rodney Brister; Timothy C Mueser; Nancy G Nossal; Deborah M Hinton
Journal:  J Biol Chem       Date:  2012-03-15       Impact factor: 5.157

5.  Single-molecule visualization of RecQ helicase reveals DNA melting, nucleation, and assembly are required for processive DNA unwinding.

Authors:  Behzad Rad; Anthony L Forget; Ronald J Baskin; Stephen C Kowalczykowski
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-04       Impact factor: 11.205

6.  Control of helicase loading in the coupled DNA replication and recombination systems of bacteriophage T4.

Authors:  Amy M Branagan; Jenny A Klein; Christian S Jordan; Scott W Morrical
Journal:  J Biol Chem       Date:  2013-12-14       Impact factor: 5.157

Review 7.  Break-induced DNA replication.

Authors:  Ranjith P Anand; Susan T Lovett; James E Haber
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-12-01       Impact factor: 10.005

8.  RNA primer handoff in bacteriophage T4 DNA replication: the role of single-stranded DNA-binding protein and polymerase accessory proteins.

Authors:  Scott W Nelson; Ravindra Kumar; Stephen J Benkovic
Journal:  J Biol Chem       Date:  2008-05-28       Impact factor: 5.157

9.  Repair of double-strand breaks in bacteriophage T4 by a mechanism that involves extensive DNA replication.

Authors:  J W George; K N Kreuzer
Journal:  Genetics       Date:  1996-08       Impact factor: 4.562

10.  Recombination-dependent DNA replication stimulated by double-strand breaks in bacteriophage T4.

Authors:  K N Kreuzer; M Saunders; L J Weislo; H W Kreuzer
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.