Literature DB >> 8156995

A developmental checkpoint couples the initiation of sporulation to DNA replication in Bacillus subtilis.

K Ireton1, A D Grossman.   

Abstract

Spore formation in Bacillus subtilis requires the generation of two distinct cell types, each with an active chromosome that becomes committed to a defined program of gene expression. Here we show that a developmental checkpoint couples the initiation of sporulation, and the subsequent formation of these two cell types, to DNA replication early during development. Inhibiting the initiation of chromosomal replication prevents the onset of sporulation and inhibits expression of several genes that are normally induced early during development. This defect in gene expression is due to inhibition of the multi-component phosphorylation pathway needed to activate the developmental transcription factor encoded by spo0A. The target affected by inhibiting the initiation of replication is neither Spo0A nor the major kinase, KinA, needed for production of Spo0A approximately P. Rather, the target appears to be one of the proteins that transfers phosphate from the kinase to the Spo0A transcription factor. The signal that couples activity of the phosphorelay to the initiation of DNA replication is different from the previously described DNA damage signal that inhibits the phosphorelay during SOS induction in a recA-dependent response. Thus, DNA replication as well as DNA damage signals control production of Spo0A approximately P and initiation of sporulation.

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Year:  1994        PMID: 8156995      PMCID: PMC394986          DOI: 10.1002/j.1460-2075.1994.tb06419.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  59 in total

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Journal:  Bacteriol Rev       Date:  1976-12

2.  The p53 tumor suppressor protein: meeting review.

Authors:  C Prives; J J Manfredi
Journal:  Genes Dev       Date:  1993-04       Impact factor: 11.361

3.  Enzyme changes during Bacillus subtilis sporulation caused by deprivation of guanine nucleotides.

Authors:  N Vasantha; E Freese
Journal:  J Bacteriol       Date:  1980-12       Impact factor: 3.490

4.  Induction of sporulation in Bacillus subtilis by decoyinine or hadacidin.

Authors:  T Mitani; J E Heinze; E Freese
Journal:  Biochem Biophys Res Commun       Date:  1977-08-08       Impact factor: 3.575

5.  Premature of chromosome condensation in a ts DNA- mutant of BHK cells.

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Journal:  Cell       Date:  1978-10       Impact factor: 41.582

6.  Fate of transforming DNA following uptake by competent Bacillus subtilis. I. Formation and properties of the donor-recipient complex.

Authors:  D Dubnau; R Davidoff-Abelson
Journal:  J Mol Biol       Date:  1971-03-14       Impact factor: 5.469

7.  Sporulation of Bacillus subtilis in continuous culture.

Authors:  I W Dawes; J Mandelstam
Journal:  J Bacteriol       Date:  1970-09       Impact factor: 3.490

8.  Sporulation in Bacillus subtilis. Effect of medium on the form of chromosome replication and on initiation to sporulation in Bacillus subtilis.

Authors:  J Mandelstam; J M Sterlini; D Kay
Journal:  Biochem J       Date:  1971-11       Impact factor: 3.857

9.  DNA-membrane association is necessary for initiation of chromosomal and plasmid replication in Bacillus subtilis.

Authors:  S Winston; N Sueoka
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

10.  Induction of sporulation during synchronized chromosome replication in Bacillus subtilis.

Authors:  J Mandelstam; S A Higgs
Journal:  J Bacteriol       Date:  1974-10       Impact factor: 3.490

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  22 in total

1.  Control of initiation of sporulation by replication initiation genes in Bacillus subtilis.

Authors:  K P Lemon; I Kurtser; J Wu; A D Grossman
Journal:  J Bacteriol       Date:  2000-05       Impact factor: 3.490

2.  Membrane topology of the Bacillus subtilis pro-sigma(K) processing complex.

Authors:  D H Green; S M Cutting
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

3.  Postexponential regulation of sin operon expression in Bacillus subtilis.

Authors:  Sasha H Shafikhani; Ines Mandic-Mulec; Mark A Strauch; Issar Smith; Terrance Leighton
Journal:  J Bacteriol       Date:  2002-01       Impact factor: 3.490

4.  CtrA mediates a DNA replication checkpoint that prevents cell division in Caulobacter crescentus.

Authors:  M Wortinger; M J Sackett; Y V Brun
Journal:  EMBO J       Date:  2000-09-01       Impact factor: 11.598

Review 5.  Compartmentalization of gene expression during Bacillus subtilis spore formation.

Authors:  David W Hilbert; Patrick J Piggot
Journal:  Microbiol Mol Biol Rev       Date:  2004-06       Impact factor: 11.056

6.  A transcriptional response to replication status mediated by the conserved bacterial replication protein DnaA.

Authors:  Alexi I Goranov; Luba Katz; Adam M Breier; Christopher B Burge; Alan D Grossman
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-24       Impact factor: 11.205

Review 7.  Controlling cell cycle and cell fate: common strategies in prokaryotes and eukaryotes.

Authors:  A Amon
Journal:  Proc Natl Acad Sci U S A       Date:  1998-01-06       Impact factor: 11.205

8.  Identification of a membrane protein involved in activation of the KinB pathway to sporulation in Bacillus subtilis.

Authors:  V Dartois; T Djavakhishvili; J A Hoch
Journal:  J Bacteriol       Date:  1996-02       Impact factor: 3.490

9.  Different roles for KinA, KinB, and KinC in the initiation of sporulation in Bacillus subtilis.

Authors:  J R LeDeaux; N Yu; A D Grossman
Journal:  J Bacteriol       Date:  1995-02       Impact factor: 3.490

10.  Krebs cycle function is required for activation of the Spo0A transcription factor in Bacillus subtilis.

Authors:  K Ireton; S Jin; A D Grossman; A L Sonenshein
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

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