Literature DB >> 6328425

Methylation dependent expression of the mom gene of bacteriophage Mu: deletions downstream from the methylation sites affect expression.

C C Adley, A I Bukhari.   

Abstract

The expression of the DNA modification gene (mom) of bacteriophage Mu requires the cellular deoxyadenosine methylase (dam) and a transactivation factor from the phage. By hypothesis, the transcription of mom is activated by methylation of three GATC sequences upstream from the mom gene. We have introduced small deletions at a fourth GATC site located about 140 base pairs downstream from the primary methylation region. Some of the deletions severely affect the mom gene expression. We propose from this analysis that (1) some important elements, possibly the promoter, concerned with the expression of mom are located between nucleotides 840 and 880 from the right end of Mu and (2) the mom protein starts with the codon GTG located at position 810. We favor the hypothesis that methylation turns off transcription upstream, thereby allowing the main mom promoter to function.

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Year:  1984        PMID: 6328425      PMCID: PMC318767          DOI: 10.1093/nar/12.8.3535

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  22 in total

1.  Analysis of bacteriophage mu and lambda-mu hybrid DNAs by specific endonucleases.

Authors:  B Allet; A I Bukhari
Journal:  J Mol Biol       Date:  1975-03-15       Impact factor: 5.469

2.  Genetic mapping of prophage Mu.

Authors:  A I Bukhari; M Metlay
Journal:  Virology       Date:  1973-07       Impact factor: 3.616

3.  Supercoiled circular DNA-protein complex in Escherichia coli: purification and induced conversion to an opern circular DNA form.

Authors:  D B Clewell; D R Helinski
Journal:  Proc Natl Acad Sci U S A       Date:  1969-04       Impact factor: 11.205

4.  Promoter occlusion: transcription through a promoter may inhibit its activity.

Authors:  S Adhya; M Gottesman
Journal:  Cell       Date:  1982-07       Impact factor: 41.582

5.  In vitro and in vivo manipulations of bacteriophage Mu DNA: cloning of Mu ends and construction of mini-Mu's carrying selectable markers.

Authors:  G Chaconas; F J de Bruijn; M J Casadaban; J R Lupski; T J Kwoh; R M Harshey; M S DuBow; A I Bukhari
Journal:  Gene       Date:  1981 Jan-Feb       Impact factor: 3.688

6.  Regulation of the DNA-modification function of bacteriophage Mu.

Authors:  S Hattman; M Goradia; C Monaghan; A I Bukhari
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1983

7.  Identification of the gin protein of bacteriophage mu.

Authors:  D Y Kwoh; D Zipser
Journal:  Virology       Date:  1981-10-15       Impact factor: 3.616

Review 8.  Eukaryotic DNA methylation.

Authors:  D N Cooper
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  The 3'-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites.

Authors:  J Shine; L Dalgarno
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205

10.  Transcription initiation of Mu mom depends on methylation of the promoter region and a phage-coded transactivator.

Authors:  R H Plasterk; H Vrieling; P Van de Putte
Journal:  Nature       Date:  1983-01-27       Impact factor: 49.962

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  2 in total

1.  The major phase-variable outer membrane protein of Escherichia coli structurally resembles the immunoglobulin A1 protease class of exported protein and is regulated by a novel mechanism involving Dam and oxyR.

Authors:  I R Henderson; P Owen
Journal:  J Bacteriol       Date:  1999-04       Impact factor: 3.490

2.  Effect of dam methylation on the activity of the E. coli replication origin, oriC.

Authors:  W Messer; U Bellekes; H Lother
Journal:  EMBO J       Date:  1985-05       Impact factor: 11.598

  2 in total

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