Literature DB >> 2553669

Molecular cloning and characterization of comC, a late competence gene of Bacillus subtilis.

S Mohan1, J Aghion, N Guillen, D Dubnau.   

Abstract

comC is a Bacillus subtilis gene required for the development of genetic competence. We have cloned a fragment from the B. subtilis chromosome that carries comC and contains all the information required to complement a Tn917lac insertion in comC. Genetic tests further localized comC to a 2.0-kilobase HindIII fragment. Northern (RNA) blotting experiments revealed that an 800-base-pair comC-specific transcript appeared at the time of transition from exponential to stationary phase during growth through the competence regimen. The DNA sequence of the comC region revealed two open reading frames (ORFs), transcribed in the same direction. The upstream ORF encoded a protein with apparent sequence similarity to the folC gene of Escherichia coli. Insertion of a chloramphenicol resistance determinant into this ORF and integration of the disrupted construct into the bacterial chromosome by replacement did not result in competence deficiency. The downstream ORF, which contained the Tn917lac insertion that resulted in a lack of competence, is therefore the comC gene. The predicted protein product of comC consisted of 248 amino acid residues and was quite hydrophobic. The comC gene product was not required for the expression of any other com genes tested, and this fact, together with the marked hydrophobicity of ComC, suggests that it may be a component of the DNA-processing apparatus of competent cells.

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Year:  1989        PMID: 2553669      PMCID: PMC210470          DOI: 10.1128/jb.171.11.6043-6051.1989

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


  27 in total

1.  REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS.

Authors:  C Anagnostopoulos; J Spizizen
Journal:  J Bacteriol       Date:  1961-05       Impact factor: 3.490

2.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

3.  Isolation and characterization of Tn917lac-generated competence mutants of Bacillus subtilis.

Authors:  J Hahn; M Albano; D Dubnau
Journal:  J Bacteriol       Date:  1987-07       Impact factor: 3.490

4.  Transformation and transduction in Bacillus subtilis: evidence for separate modes of recombinant formation.

Authors:  D Dubnau; R Davidoff-Abelson; I Smith
Journal:  J Mol Biol       Date:  1969-10-28       Impact factor: 5.469

5.  Sequence and transcription mapping of Bacillus subtilis competence genes comB and comA, one of which is related to a family of bacterial regulatory determinants.

Authors:  Y Weinrauch; N Guillen; D A Dubnau
Journal:  J Bacteriol       Date:  1989-10       Impact factor: 3.490

6.  Evolutionary relationships of the Bacillus licheniformis macrolide-lincosamide-streptogramin B resistance elements.

Authors:  M Israeli-Reches; Y Weinrauch; D Dubnau
Journal:  Mol Gen Genet       Date:  1984

7.  A novel method for the rapid cloning in Escherichia coli of Bacillus subtilis chromosomal DNA adjacent to Tn917 insertions.

Authors:  P Youngman; J B Perkins; R Losick
Journal:  Mol Gen Genet       Date:  1984

8.  Replication and incompatibility properties of plasmid pE194 in Bacillus subtilis.

Authors:  T J Gryczan; J Hahn; S Contente; D Dubnau
Journal:  J Bacteriol       Date:  1982-11       Impact factor: 3.490

9.  A rapid single-stranded cloning strategy for producing a sequential series of overlapping clones for use in DNA sequencing: application to sequencing the corn mitochondrial 18 S rDNA.

Authors:  R M Dale; B A McClure; J P Houchins
Journal:  Plasmid       Date:  1985-01       Impact factor: 3.466

10.  Complete nucleotide sequence of macrolide-lincosamide-streptogramin B-resistance transposon Tn917 in Streptococcus faecalis.

Authors:  J H Shaw; D B Clewell
Journal:  J Bacteriol       Date:  1985-11       Impact factor: 3.490

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  29 in total

1.  Twelve pil genes are required for biogenesis of the R64 thin pilus.

Authors:  T Yoshida; S R Kim; T Komano
Journal:  J Bacteriol       Date:  1999-04       Impact factor: 3.490

2.  Biogenesis of a putative channel protein, ComEC, required for DNA uptake: membrane topology, oligomerization and formation of disulphide bonds.

Authors:  Irena Draskovic; David Dubnau
Journal:  Mol Microbiol       Date:  2005-02       Impact factor: 3.501

3.  Sequence and transcriptional regulation of com101A, a locus required for genetic transformation in Haemophilus influenzae.

Authors:  T G Larson; S H Goodgal
Journal:  J Bacteriol       Date:  1991-08       Impact factor: 3.490

4.  All seven comG open reading frames are required for DNA binding during transformation of competent Bacillus subtilis.

Authors:  Y S Chung; D Dubnau
Journal:  J Bacteriol       Date:  1998-01       Impact factor: 3.490

5.  Molecular analyses of the natural transformation machinery and identification of pilus structures in the extremely thermophilic bacterium Thermus thermophilus strain HB27.

Authors:  Alexandra Friedrich; Christina Prust; Thomas Hartsch; Anke Henne; Beate Averhoff
Journal:  Appl Environ Microbiol       Date:  2002-02       Impact factor: 4.792

6.  Type IV pilus genes pilA and pilC of Pseudomonas stutzeri are required for natural genetic transformation, and pilA can be replaced by corresponding genes from nontransformable species.

Authors:  S Graupner; V Frey; R Hashemi; M G Lorenz; G Brandes; W Wackernagel
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

7.  Sporulation gene spoIIB from Bacillus subtilis.

Authors:  P S Margolis; A Driks; R Losick
Journal:  J Bacteriol       Date:  1993-01       Impact factor: 3.490

8.  Identification of the hopG gene, a component of Escherichia coli K-12 type II export system, and its conservation among different pathogenic Escherichia coli and Shigella isolates.

Authors:  I Stojiljkovic; R Schönherr; J G Kusters
Journal:  J Bacteriol       Date:  1995-04       Impact factor: 3.490

9.  Production of Neisseria gonorrhoeae pili (fimbriae) in Pseudomonas aeruginosa.

Authors:  P A Hoyne; R Haas; T F Meyer; J K Davies; T C Elleman
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

10.  Product of the Pseudomonas aeruginosa gene pilD is a prepilin leader peptidase.

Authors:  D N Nunn; S Lory
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-15       Impact factor: 11.205

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