Literature DB >> 6757658

Suppressor mutations (rin) that specifically suppress the recA+ dependence of stable DNA replication in Escherichia coliK-12.

T A Torrey, T Kogoma.   

Abstract

The sdrA102 mutation confers upon cells the ability to replicate DNA in the absence of protein synthesis. This mutation was combined with the recA200 mutation, which renders the recA protein thermolabile, and had little effect on normal replication. However, the sdrA102 recA200 double mutant exhibited temperature-sensitive stable DNA replication: it replicated DNA continuously in the presence of chloramphenicol at 30 degrees C, whereas at 42 degrees C DNA replication ceased after the DNA content increased only 40-45%. Suppressor mutants (rin; recA-independent) capable of stable DNA replication at 42 degrees C were isolated from the double mutant. The suppressor mutant retained all other recA- characteristics, i.e., deficient general recombination, severe UV-sensitivity, and incapability of prophage induction in lysogens. This indicates that the rin mutation specifically suppresses the recA+ dependency of stable DNA replication. It is suggested that the recA+ protein stabilizes a specific structure, similar to an intermediate in recombination, which may function in the initiation of stable DNA replication.

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Year:  1982        PMID: 6757658     DOI: 10.1007/bf00331121

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  31 in total

1.  Characterization of the replication of Escherichia coli DNA in the absence of protein synthesis: stable DNA replication.

Authors:  T Kogoma; K G Lark
Journal:  J Mol Biol       Date:  1975-05-15       Impact factor: 5.469

2.  Characteristics of purified recA protein and the regulation of its synthesis in vivo.

Authors:  T Ogawa; H Wabiko; T Tsurimoto; T Horii; H Masukata; H Ogawa
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1979

3.  Genetic Map of Bacteriophage phiX174.

Authors:  R M Benbow; C A Hutchison; J D Fabricant; R L Sinsheimer
Journal:  J Virol       Date:  1971-05       Impact factor: 5.103

4.  Plasmids carrying oriC can integrate at or near the chromosome origin of Escherichia coli in the absence of a functional recA product.

Authors:  M Masters; V Andresdottir; H Wolf-Watz
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1979

5.  Characteristics of some multiply recombination-deficient strains of Escherichia coli.

Authors:  N S Willetts; A J Clark
Journal:  J Bacteriol       Date:  1969-10       Impact factor: 3.490

Review 6.  Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli.

Authors:  E M Witkin
Journal:  Bacteriol Rev       Date:  1976-12

7.  Site-specific integration of an F' lac pro factor in the region of the replication origin (oriC) of E. coli.

Authors:  L S LaVerne; D S Ray
Journal:  Mol Gen Genet       Date:  1980

8.  Construction of an Hfr strain useful for transferring recA mutations between Escherichia coli strains.

Authors:  L N Csonka; A J Clark
Journal:  J Bacteriol       Date:  1980-07       Impact factor: 3.490

9.  Cleavage of the Escherichia coli lexA protein by the recA protease.

Authors:  J W Little; S H Edmiston; L Z Pacelli; D W Mount
Journal:  Proc Natl Acad Sci U S A       Date:  1980-06       Impact factor: 11.205

10.  Expression of the E. coli uvrA gene is inducible.

Authors:  C J Kenyon; G C Walker
Journal:  Nature       Date:  1981-02-26       Impact factor: 49.962

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  23 in total

1.  A combination of RNase H (rnh) and recBCD or sbcB mutations in Escherichia coli K12 adversely affects growth.

Authors:  M Itaya; R J Crouch
Journal:  Mol Gen Genet       Date:  1991-07

2.  Correlation of activity with phenotypes of Escherichia coli partial function mutants of rnh, the gene encoding RNase H.

Authors:  M Itaya; R J Crouch
Journal:  Mol Gen Genet       Date:  1991-07

3.  Initiation of chromosomal DNA replication which is stimulated without oversupply of DnaA protein in Escherichia coli.

Authors:  T Katayama; T Nagata
Journal:  Mol Gen Genet       Date:  1991-05

4.  Mode of initiation of constitutive stable DNA replication in RNase H-defective mutants of Escherichia coli K-12.

Authors:  K von Meyenburg; E Boye; K Skarstad; L Koppes; T Kogoma
Journal:  J Bacteriol       Date:  1987-06       Impact factor: 3.490

5.  Genetic analysis of constitutive stable DNA replication in rnh mutants of Escherichia coli K12.

Authors:  T A Torrey; T Kogoma
Journal:  Mol Gen Genet       Date:  1987-07

6.  Function of ribonuclease H in initiation of DNA replication in Escherichia coli K-12.

Authors:  T Kogoma; N L Subia; K von Meyenburg
Journal:  Mol Gen Genet       Date:  1985

7.  RecA protein acts at the initiation of stable DNA replication in rnh mutants of Escherichia coli K-12.

Authors:  T Kogoma; K Skarstad; E Boye; K von Meyenburg; H B Steen
Journal:  J Bacteriol       Date:  1985-08       Impact factor: 3.490

8.  RNase H is not involved in the induction of stable DNA replication in Escherichia coli.

Authors:  H Bialy; T Kogoma
Journal:  J Bacteriol       Date:  1986-01       Impact factor: 3.490

Review 9.  RNase H-defective mutants of Escherichia coli.

Authors:  T Kogoma
Journal:  J Bacteriol       Date:  1986-05       Impact factor: 3.490

Review 10.  Stable DNA replication: interplay between DNA replication, homologous recombination, and transcription.

Authors:  T Kogoma
Journal:  Microbiol Mol Biol Rev       Date:  1997-06       Impact factor: 11.056

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