Literature DB >> 1731202

DNA twisting and the effects of non-contacted bases on affinity of 434 operator for 434 repressor.

G B Koudelka1, P Carlson.   

Abstract

The bacteriophage 434 repressor regulates gene expression by binding with differing affinities to the six operator sites on the phage chromosome. The symmetrically arrayed outer eight base pairs (four in each half-site) of these 14-base-pair operators are highly conserved but the middle four bases are divergent. Although these four base pairs are not in contact with repressor, operators with A.T or T.A base pairs at these positions bind repressor more strongly than those bearing C.G or G.C, suggesting that these bases are important for the repressor's ability to discriminate between operators. There is evidence that the central base pairs influence operator function by constraining the twisting and/or bending of DNA. Here we show that there is a relationship between the intrinsic twist of an operator, as determined by the sequence of its central bases, and its affinity for repressor; an operator with a lower affinity is undertwisted relative to an operator with higher affinity. In complex with repressor, the twist of both high- and low-affinity operators is the same. These results indicate that the intrinsic twist of DNA and its twisting flexibility both affect the affinity of 434 operator for repressor.

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Year:  1992        PMID: 1731202     DOI: 10.1038/355089a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  25 in total

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Authors:  M Ouhammouch; E P Geiduschek
Journal:  EMBO J       Date:  2001-01-15       Impact factor: 11.598

2.  Predicting indirect readout effects in protein-DNA interactions.

Authors:  Yongli Zhang; Zhiqun Xi; Rashmi S Hegde; Zippora Shakked; Donald M Crothers
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-17       Impact factor: 11.205

Review 3.  Origins of specificity in protein-DNA recognition.

Authors:  Remo Rohs; Xiangshu Jin; Sean M West; Rohit Joshi; Barry Honig; Richard S Mann
Journal:  Annu Rev Biochem       Date:  2010       Impact factor: 23.643

4.  Indirect readout of DNA sequence at the primary-kink site in the CAP-DNA complex: recognition of pyrimidine-purine and purine-purine steps.

Authors:  Andrew A Napoli; Catherine L Lawson; Richard H Ebright; Helen M Berman
Journal:  J Mol Biol       Date:  2006-01-03       Impact factor: 5.469

5.  Effect of salt shock on stability of lambdaimm434 lysogens.

Authors:  Paul Shkilnyj; Gerald B Koudelka
Journal:  J Bacteriol       Date:  2007-02-16       Impact factor: 3.490

6.  Targeted chemical wedges reveal the role of allosteric DNA modulation in protein-DNA assembly.

Authors:  Rocco Moretti; Leslie J Donato; Mary L Brezinski; Ryan L Stafford; Helena Hoff; Jon S Thorson; Peter B Dervan; Aseem Z Ansari
Journal:  ACS Chem Biol       Date:  2008-04-18       Impact factor: 5.100

7.  Recognition of DNA structure by 434 repressor.

Authors:  G B Koudelka
Journal:  Nucleic Acids Res       Date:  1998-01-15       Impact factor: 16.971

8.  Dimerization specificity of P22 and 434 repressors is determined by multiple polypeptide segments.

Authors:  A L Donner; P A Carlson; G B Koudelka
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

9.  Recognition of DNA by single-chain derivatives of the phage 434 repressor: high affinity binding depends on both the contacted and non-contacted base pairs.

Authors:  J Chen; S Pongor; A Simoncsits
Journal:  Nucleic Acids Res       Date:  1997-06-01       Impact factor: 16.971

10.  Structure of the LexA-DNA complex and implications for SOS box measurement.

Authors:  Adrianna P P Zhang; Ying Z Pigli; Phoebe A Rice
Journal:  Nature       Date:  2010-08-12       Impact factor: 49.962

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