Literature DB >> 7037745

Powerful mutator activity of the polA1 mutation within the histidine region of Escherichia coli K-12.

D J Savić, S P Romac.   

Abstract

We examined 122 spontaneous histidine auxotrophs accumulated in overnight cultures of polA1 strains of Escherichia coli K-12 at approximate frequencies of 10(-3). One hundred and thirteen appeared to be minus frameshifts, and nine appeared to be deletions. Of the frameshift mutations, 109 affected the hisC gene, and 4 affected genes hisD, hisH, hisA, and hisI. The lack of base substitutions supported the idea that polymerase-defective polA is a minus frameshift- and deletion-type mutator. Contrary to a previous report, we did not observe superior growth of PolA auxotrophs over their prototrophic progenitors (15 auxotrophs tested). We conclude that the polA1 mutation exerts a powerful mutator activity in this specific genetic context.

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Year:  1982        PMID: 7037745      PMCID: PMC216483          DOI: 10.1128/jb.149.3.955-960.1982

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  19 in total

1.  Evidence for the control by exrA and polA genes of two branches of the uvr gene-dependent excision repair pathway in Escherichia coli K-12.

Authors:  D A Youngs; K C Smith
Journal:  J Bacteriol       Date:  1973-10       Impact factor: 3.490

2.  Frameshift suppressors. 3. Effects of suppressor mutations on transfer RNA.

Authors:  D L Riddle; J R Roth
Journal:  J Mol Biol       Date:  1972-05-28       Impact factor: 5.469

3.  Chemical carcinogens as frameshift mutagens: Salmonella DNA sequence sensitive to mutagenesis by polycyclic carcinogens.

Authors:  K Isono; J Yourno
Journal:  Proc Natl Acad Sci U S A       Date:  1974-05       Impact factor: 11.205

4.  Auxotroph accumulation in deoxyribonucleic acid polymeraseless strains of Escherichia coli K-12.

Authors:  C M Berg
Journal:  J Bacteriol       Date:  1971-06       Impact factor: 3.490

5.  Increased frequency of deletions in DNA polymerase mutants of Escherichia coli.

Authors:  M B Coukell; C Yanofsky
Journal:  Nature       Date:  1970-11-14       Impact factor: 49.962

6.  Formation of merodiploids in matings with a class of Rec- recipient strains of Escherichia coli K12.

Authors:  B Low
Journal:  Proc Natl Acad Sci U S A       Date:  1968-05       Impact factor: 11.205

7.  Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday.

Authors:  G Streisinger; Y Okada; J Emrich; J Newton; A Tsugita; E Terzaghi; M Inouye
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1966

Review 8.  Classification and mapping of spontaneous and induced mutations in the histidine operon of Salmonella.

Authors:  P E Hartman; Z Hartman; R C Stahl
Journal:  Adv Genet       Date:  1971       Impact factor: 1.944

9.  Genetic map position of the gluconate-6-phosphate dehydrogenase gene in Salmonella typhimurium.

Authors:  M L Murray; T Klopotowski
Journal:  J Bacteriol       Date:  1968-04       Impact factor: 3.490

10.  ICR-induced frameshift mutations in the histidine operon of Salmonella.

Authors:  N S Oeschger; P E Hartman
Journal:  J Bacteriol       Date:  1970-02       Impact factor: 3.490

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  4 in total

1.  The roles of Klenow processing and flap processing activities of DNA polymerase I in chromosome instability in Escherichia coli K12 strains.

Authors:  Yuki Nagata; Kazumi Mashimo; Masakado Kawata; Kazuo Yamamoto
Journal:  Genetics       Date:  2002-01       Impact factor: 4.562

2.  DNA sequence analysis of spontaneous histidine mutations in a polA1 strain of Escherichia coli K12 suggests a specific role of the GTGG sequence.

Authors:  M Jankovic; T Kostic; D J Savic
Journal:  Mol Gen Genet       Date:  1990-09

3.  DNA sequence analysis of spontaneous mutation in a PolA1 strain of Escherichia coli indicates sequence-specific effects.

Authors:  D F Fix; P A Burns; B W Glickman
Journal:  Mol Gen Genet       Date:  1987-05

4.  A new mutation in Escherichia coli K12, isfA, which is responsible for inhibition of SOS functions.

Authors:  A Bebenek; I Pietrzykowska
Journal:  Mol Gen Genet       Date:  1995-07-22
  4 in total

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