Literature DB >> 12270822

Adaptive, or stationary-phase, mutagenesis, a component of bacterial differentiation in Bacillus subtilis.

Huang-Mo Sung1, Ronald E Yasbin.   

Abstract

Adaptive (stationary-phase) mutagenesis occurs in the gram-positive bacterium Bacillus subtilis. Furthermore, taking advantage of B. subtilis as a paradigm for the study of prokaryotic differentiation and development, we have shown that this type of mutagenesis is subject to regulation involving at least two of the genes that are involved in the regulation of post-exponential phase prokaryotic differentiation, i.e., comA and comK. On the other hand, a functional RecA protein was not required for this type of mutagenesis. The results seem to suggest that a small subpopulation(s) of the culture is involved in adaptive mutagenesis and that this subpopulation(s) is hypermutable. The existence of such a hypermutable subpopulation(s) raises important considerations with respect to evolution, the development of specific mutations, the nature of bacterial populations, and the level of communication among bacteria in an ecological niche.

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Year:  2002        PMID: 12270822      PMCID: PMC139596          DOI: 10.1128/JB.184.20.5641-5653.2002

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


  77 in total

Review 1.  Mechanisms of genome-wide hypermutation in stationary phase.

Authors:  M J Lombardo; J Torkelson; H J Bull; G J McKenzie; S M Rosenberg
Journal:  Ann N Y Acad Sci       Date:  1999-05-18       Impact factor: 5.691

2.  The SOS response regulates adaptive mutation.

Authors:  G J McKenzie; R S Harris; P L Lee; S M Rosenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

3.  Adaptive amplification: an inducible chromosomal instability mechanism.

Authors:  P J Hastings; H J Bull; J R Klump; S M Rosenberg
Journal:  Cell       Date:  2000-11-22       Impact factor: 41.582

4.  The contribution of bacterial hypermutators to mutation in stationary phase.

Authors:  J Cairns
Journal:  Genetics       Date:  2000-10       Impact factor: 4.562

5.  Whole-genome analysis of genes regulated by the Bacillus subtilis competence transcription factor ComK.

Authors:  Mitsuo Ogura; Hirotake Yamaguchi; Kazuo Kobayashi; Naotake Ogasawara; Yasutaro Fujita; Teruo Tanaka
Journal:  J Bacteriol       Date:  2002-05       Impact factor: 3.490

6.  General stress transcription factor sigmaB and sporulation transcription factor sigmaH each contribute to survival of Bacillus subtilis under extreme growth conditions.

Authors:  T A Gaidenko; C W Price
Journal:  J Bacteriol       Date:  1998-07       Impact factor: 3.490

7.  Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs.

Authors:  P L Foster; J M Trimarchi
Journal:  Science       Date:  1994-07-15       Impact factor: 47.728

8.  Adaptive mutation and slow-growing revertants of an Escherichia coli lacZ amber mutant.

Authors:  M J Prival; T A Cebula
Journal:  Genetics       Date:  1996-12       Impact factor: 4.562

9.  Cloning and characterization of DNA damage-inducible promoter regions from Bacillus subtilis.

Authors:  D L Cheo; K W Bayles; R E Yasbin
Journal:  J Bacteriol       Date:  1991-03       Impact factor: 3.490

Review 10.  Genetic competence in Bacillus subtilis.

Authors:  D Dubnau
Journal:  Microbiol Rev       Date:  1991-09
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  56 in total

1.  Stochastic processes influence stationary-phase decisions in Bacillus subtilis.

Authors:  Heather Maughan; Wayne L Nicholson
Journal:  J Bacteriol       Date:  2004-04       Impact factor: 3.490

2.  Transcriptional de-repression and Mfd are mutagenic in stressed Bacillus subtilis cells.

Authors:  Holly Anne Martin; Mario Pedraza-Reyes; Ronald E Yasbin; Eduardo A Robleto
Journal:  J Mol Microbiol Biotechnol       Date:  2012-01-13

3.  A high-frequency mutation in Bacillus subtilis: requirements for the decryptification of the gudB glutamate dehydrogenase gene.

Authors:  Katrin Gunka; Stefan Tholen; Jan Gerwig; Christina Herzberg; Jörg Stülke; Fabian M Commichau
Journal:  J Bacteriol       Date:  2011-12-16       Impact factor: 3.490

4.  Transcription-associated mutation in Bacillus subtilis cells under stress.

Authors:  Christine Pybus; Mario Pedraza-Reyes; Christian A Ross; Holly Martin; Katherine Ona; Ronald E Yasbin; Eduardo Robleto
Journal:  J Bacteriol       Date:  2010-04-30       Impact factor: 3.490

5.  Nutritional control of elongation of DNA replication by (p)ppGpp.

Authors:  Jue D Wang; Glenn M Sanders; Alan D Grossman
Journal:  Cell       Date:  2007-03-09       Impact factor: 41.582

6.  Stress-Induced Mutagenesis: Implications in Cancer and Drug Resistance.

Authors:  Devon M Fitzgerald; P J Hastings; Susan M Rosenberg
Journal:  Annu Rev Cancer Biol       Date:  2017-03

7.  Roles of YqjH and YqjW, homologs of the Escherichia coli UmuC/DinB or Y superfamily of DNA polymerases, in stationary-phase mutagenesis and UV-induced mutagenesis of Bacillus subtilis.

Authors:  Huang-Mo Sung; Gabriel Yeamans; Christian A Ross; Ronald E Yasbin
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

8.  Emergence of antibiotic resistance from multinucleated bacterial filaments.

Authors:  Julia Bos; Qiucen Zhang; Saurabh Vyawahare; Elizabeth Rogers; Susan M Rosenberg; Robert H Austin
Journal:  Proc Natl Acad Sci U S A       Date:  2014-12-09       Impact factor: 11.205

9.  Extent of genetic lesions of the arginine and pyrimidine biosynthetic pathways in Lactobacillus plantarum, L. paraplantarum, L. pentosus, and L. casei: prevalence of CO(2)-dependent auxotrophs and characterization of deficient arg genes in L. plantarum.

Authors:  Françoise Bringel; Jean-Claude Hubert
Journal:  Appl Environ Microbiol       Date:  2003-05       Impact factor: 4.792

10.  Role of the Nfo and ExoA apurinic/apyrimidinic endonucleases in repair of DNA damage during outgrowth of Bacillus subtilis spores.

Authors:  Juan R Ibarra; Alma D Orozco; Juan A Rojas; Karina López; Peter Setlow; Ronald E Yasbin; Mario Pedraza-Reyes
Journal:  J Bacteriol       Date:  2008-01-18       Impact factor: 3.490

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