Literature DB >> 8415741

A single-base-pair mutation changes the specificities of both a transcription activation protein and its binding site.

D M Retallack1, L L Johnson, S F Ziegler, M A Strauch, D I Friedman.   

Abstract

The C1 protein of bacteriophage P22 binds to a unique site in the -35 region of the PRE promoter and activates transcription of the phage c2 repressor gene. This -35 target has an approximate direct repeat that overlaps the 5' end of the c1 coding region. We have isolated a single-base-pair mutation in this region that changes the PRE -35 target as well as the amino-terminal region of the C1 protein. Although the mutant C1 protein activates the mutant PRE promoter, it fails to activate the wild-type PRE promoter. This suggests that a single-base-pair mutation changes the specificities of both a protein and its target site. These studies also indicate that C1 binding to DNA is influenced by contacts made through residues near the amino terminus.

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Year:  1993        PMID: 8415741      PMCID: PMC47609          DOI: 10.1073/pnas.90.20.9562

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  25 in total

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Authors:  M LEVINE
Journal:  Virology       Date:  1957-02       Impact factor: 3.616

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Authors:  S Adhya; W Miller
Journal:  Nature       Date:  1979-06-07       Impact factor: 49.962

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Authors:  S Hilliker; D Botstein
Journal:  J Mol Biol       Date:  1976-09-25       Impact factor: 5.469

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Authors:  D Botstein; I Herskowitz
Journal:  Nature       Date:  1974-10-18       Impact factor: 49.962

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Authors:  C O Pabo; R T Sauer
Journal:  Annu Rev Biochem       Date:  1984       Impact factor: 23.643

6.  Differential effects of mutations on discrete steps in transcription initiation at the lambda PRE promoter.

Authors:  M C Shih; G N Gussin
Journal:  Cell       Date:  1983-10       Impact factor: 41.582

7.  Homology among DNA-binding proteins suggests use of a conserved super-secondary structure.

Authors:  R T Sauer; R R Yocum; R F Doolittle; M Lewis; C O Pabo
Journal:  Nature       Date:  1982-07-29       Impact factor: 49.962

8.  Sequence analysis of a region from the early right operon in phage P22 including the replication genes 18 and 12.

Authors:  H Backhaus; J B Petri
Journal:  Gene       Date:  1984-12       Impact factor: 3.688

9.  Bacteriophage lambda protein cII binds promoters on the opposite face of the DNA helix from RNA polymerase.

Authors:  Y S Ho; D L Wulff; M Rosenberg
Journal:  Nature       Date:  1983 Aug 25-31       Impact factor: 49.962

10.  Formation of hybrids between coliphage lambda and Salmonella phage P22 with a Salmonella typhimurium hybrid sensitive to these phages.

Authors:  P Gemski; L S Baron; N Yamamoto
Journal:  Proc Natl Acad Sci U S A       Date:  1972-11       Impact factor: 11.205

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  4 in total

1.  Structure of lambda CII: implications for recognition of direct-repeat DNA by an unusual tetrameric organization.

Authors:  Ajit B Datta; Santosh Panjikar; Manfred S Weiss; Pinak Chakrabarti; Pradeep Parrack
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-01       Impact factor: 11.205

2.  Phage HK022 Roi protein inhibits phage lytic growth in Escherichia coli integration host factor mutants.

Authors:  M Clerget; F Boccard
Journal:  J Bacteriol       Date:  1996-07       Impact factor: 3.490

3.  Role for 10Sa RNA in the growth of lambda-P22 hybrid phage.

Authors:  D M Retallack; L L Johnson; D I Friedman
Journal:  J Bacteriol       Date:  1994-04       Impact factor: 3.490

4.  Crystallization and X-ray analysis of the transcription-activator protein C1 of bacteriophage P22 in complex with the PRE promoter element.

Authors:  Avisek Mondal; Rajagopal Chattopadhyaya; Ajit Bikram Datta; Pradeep Parrack
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2015-09-23       Impact factor: 1.056

  4 in total

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