Literature DB >> 8021191

The dacF-spoIIA operon of Bacillus subtilis, encoding sigma F, is autoregulated.

R Schuch1, P J Piggot.   

Abstract

The spoIIA operon of Bacillus subtilis encodes sigma F and two proteins that may regulate sigma factor activity. High level induction of the tricistronic spoIIA operon occurs early during spore formation. At later times, the locus is cotranscribed with the upstream gene dacF, which encodes a putative DD-carboxypeptidase. In this study, the regulation of dacF-spoIIA transcription has been analyzed. Expression of a dacF-lacZ transcriptional fusion during sporulation required sigma F but not the later-expressed sporulation-associated sigma factors. Induction of sigma F synthesis during vegetative growth caused expression of dacF-lacZ fusions. The dacF-spoIIA promoter sequence is similar to sequences of previously identified sigma F promoters. It is concluded that dacF-spoIIA is transcribed by E sigma F. We present evidence that dacF-spoIIA is also transcribed by E sigma G, as is the case for the three other promoters known to be transcribed by E sigma F.

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Year:  1994        PMID: 8021191      PMCID: PMC205609          DOI: 10.1128/jb.176.13.4104-4110.1994

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


  45 in total

1.  Identification of different sites of expression for spo loci by transformation of Bacillus subtilis.

Authors:  H de Lencastre; P J Piggot
Journal:  J Gen Microbiol       Date:  1979-10

Review 2.  Genetic aspects of bacterial endospore formation.

Authors:  P J Piggot; J G Coote
Journal:  Bacteriol Rev       Date:  1976-12

3.  Effect of chromosome location of Bacillus subtilis forespore genes on their spo gene dependence and transcription by E sigma F: identification of features of good E sigma F-dependent promoters.

Authors:  D Sun; P Fajardo-Cavazos; M D Sussman; F Tovar-Rojo; R M Cabrera-Martinez; P Setlow
Journal:  J Bacteriol       Date:  1991-12       Impact factor: 3.490

4.  Mapping of asporogenous mutations of Bacillus subtilis: a minimum estimate of the number of sporeulation operons.

Authors:  P J Piggot
Journal:  J Bacteriol       Date:  1973-06       Impact factor: 3.490

5.  Nucleotide sequence of sporulation locus spoIIA in Bacillus subtilis.

Authors:  P Fort; P J Piggot
Journal:  J Gen Microbiol       Date:  1984-08

6.  Statistical estimate of the total number of operons specific for Bacillus subtilis sporulation.

Authors:  D Hranueli; P J Piggot; J Mandelstam
Journal:  J Bacteriol       Date:  1974-09       Impact factor: 3.490

7.  Symposium on bacterial spores: II. Genetics of sporulation in Bacillus subtilis Marburg.

Authors:  H Ionesco; J Michel; B Cami; P Schaeffer
Journal:  J Appl Bacteriol       Date:  1970-03

8.  Use of the Escherichia coli lac repressor and operator to control gene expression in Bacillus subtilis.

Authors:  D G Yansura; D J Henner
Journal:  Proc Natl Acad Sci U S A       Date:  1984-01       Impact factor: 11.205

9.  Use of integrational plasmid vectors to demonstrate the polycistronic nature of a transcriptional unit (spoIIA) required for sporulation of Bacillus subtilis.

Authors:  P J Piggot; C A Curtis; H de Lencastre
Journal:  J Gen Microbiol       Date:  1984-08

10.  Isolation and characterization of a recombinant plasmid carrying a functional part of the Bacillus subtilis spoIIA locus.

Authors:  H M Liu; K F Chak; P J Piggot
Journal:  J Gen Microbiol       Date:  1982-11
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  23 in total

1.  The "pro" sequence of the sporulation-specific sigma transcription factor sigma(E) directs it to the mother cell side of the sporulation septum.

Authors:  J Ju; W G Haldenwang
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

2.  Identification and characterization of a new prespore-specific regulatory gene, rsfA, of Bacillus subtilis.

Authors:  L J Wu; J Errington
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

3.  The chromosomal location of the Bacillus subtilis sporulation gene spoIIR is important for its function.

Authors:  A Khvorova; V K Chary; D W Hilbert; P J Piggot
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

4.  Inactivation of σE and σG in Clostridium acetobutylicum illuminates their roles in clostridial-cell-form biogenesis, granulose synthesis, solventogenesis, and spore morphogenesis.

Authors:  Bryan P Tracy; Shawn W Jones; Eleftherios T Papoutsakis
Journal:  J Bacteriol       Date:  2011-01-07       Impact factor: 3.490

5.  Blocking chromosome translocation during sporulation of Bacillus subtilis can result in prespore-specific activation of sigmaG that is independent of sigmaE and of engulfment.

Authors:  Vasant K Chary; Panagiotis Xenopoulos; Patrick J Piggot
Journal:  J Bacteriol       Date:  2006-10       Impact factor: 3.490

6.  Distinctive topologies of partner-switching signaling networks correlate with their physiological roles.

Authors:  Oleg A Igoshin; Margaret S Brody; Chester W Price; Michael A Savageau
Journal:  J Mol Biol       Date:  2007-04-14       Impact factor: 5.469

7.  Roles of low-molecular-weight penicillin-binding proteins in Bacillus subtilis spore peptidoglycan synthesis and spore properties.

Authors:  D L Popham; M E Gilmore; P Setlow
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

8.  Development of a two-part transcription probe to determine the completeness of temporal and spatial compartmentalization of gene expression during bacterial development.

Authors:  Z Li; P J Piggot
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-16       Impact factor: 11.205

9.  The cytochrome bc complex (menaquinone:cytochrome c reductase) in Bacillus subtilis has a nontraditional subunit organization.

Authors:  J Yu; L Hederstedt; P J Piggot
Journal:  J Bacteriol       Date:  1995-12       Impact factor: 3.490

Review 10.  The sigma factors of Bacillus subtilis.

Authors:  W G Haldenwang
Journal:  Microbiol Rev       Date:  1995-03
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