Literature DB >> 3403531

Deletion analysis of bacteriophage T4 tertiary origins. A promoter sequence is required for a rifampicin-resistant replication origin.

A E Menkens1, K N Kreuzer.   

Abstract

The DNA sequence requirements of two T4 tertiary replication origins have been characterized by a deletion analysis of origin-containing plasmids. Maximal replication of each origin-containing plasmid required both an intact gpmotA-dependent middle-mode promoter sequence and approximately 50 base pairs of the downstream region. In contrast, gpmotA-dependent transcription from the origin promoter was found to be independent of the downstream region. The requirement for a promoter element within the tertiary origins is striking, particularly since the replication of tertiary origin-containing plasmids is resistant to the RNA polymerase inhibitor rifampicin.

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Year:  1988        PMID: 3403531

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


  22 in total

1.  An antitumor drug-induced topoisomerase cleavage complex blocks a bacteriophage T4 replication fork in vivo.

Authors:  G Hong; K N Kreuzer
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

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.  Multiple origins of replication contribute to a discontinuous pattern of DNA synthesis across the T4 genome during infection.

Authors:  J Rodney Brister; Nancy G Nossal
Journal:  J Mol Biol       Date:  2007-02-09       Impact factor: 5.469

4.  Requirement of RecBC enzyme and an elevated level of activated RecA for induced stable DNA replication in Escherichia coli.

Authors:  T R Magee; T Kogoma
Journal:  J Bacteriol       Date:  1990-04       Impact factor: 3.490

5.  DNA polymerase of bacteriophage T4 is an autogenous translational repressor.

Authors:  M Andrake; N Guild; T Hsu; L Gold; C Tuerk; J Karam
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

6.  Two types of recombination hotspots in bacteriophage T4: one requires DNA damage and a replication origin and the other does not.

Authors:  P L Doan; K G Belanger; K N Kreuzer
Journal:  Genetics       Date:  2001-03       Impact factor: 4.562

7.  Substitutions in bacteriophage T4 AsiA and Escherichia coli sigma(70) that suppress T4 motA activation mutations.

Authors:  M P Cicero; M M Sharp; C A Gross; K N Kreuzer
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

8.  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

9.  The specificity of topoisomerase-mediated DNA cleavage defines acridine-induced frameshift specificity within a hotspot in bacteriophage T4.

Authors:  M Masurekar; K N Kreuzer; L S Ripley
Journal:  Genetics       Date:  1991-03       Impact factor: 4.562

Review 10.  Transcriptional control in the prereplicative phase of T4 development.

Authors:  Deborah M Hinton
Journal:  Virol J       Date:  2010-10-28       Impact factor: 4.099

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