Literature DB >> 8846224

Dramatic changes in DNA-binding specificity caused by single residue substitutions in an Arc/Mnt hybrid repressor.

B E Raumann1, K L Knight, R T Sauer.   

Abstract

Arc and Mnt are homologous repressors which recognize operator sequences that differ at 8-10 important positions. Nevertheless, single residue changes in an Arc/Mnt hybrid protein can switch DNA-binding specificity between the two operators and even allow one particular hybrid to bind strongly to both operators. The ability of single residue changes to radically alter binding specificity involves: 'master' residues that mediate some base contacts directly and some base contacts indirectly through residue-residue hydrogen bonds; identical residues which can make alternative sets of DNA contacts in the two operators; and amplification of the effect of each mutation because the proteins bind operator DNA as tetramers.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8846224     DOI: 10.1038/nsb1295-1115

Source DB:  PubMed          Journal:  Nat Struct Biol        ISSN: 1072-8368


  11 in total

1.  Non-independence of Mnt repressor-operator interaction determined by a new quantitative multiple fluorescence relative affinity (QuMFRA) assay.

Authors:  T K Man; G D Stormo
Journal:  Nucleic Acids Res       Date:  2001-06-15       Impact factor: 16.971

2.  Physical constraints and functional characteristics of transcription factor-DNA interaction.

Authors:  Ulrich Gerland; J David Moroz; Terence Hwa
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-06       Impact factor: 11.205

3.  Swapping single-stranded DNA sequence specificities of relaxases from conjugative plasmids F and R100.

Authors:  Matthew J Harley; Joel F Schildbach
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-22       Impact factor: 11.205

4.  Quantitative modeling of DNA-protein interactions: effects of amino acid substitutions on binding specificity of the Mnt repressor.

Authors:  Tsz-Kwong Man; Joshua SungWoo Yang; Gary D Stormo
Journal:  Nucleic Acids Res       Date:  2004-08-02       Impact factor: 16.971

5.  Percolation of the phd repressor-operator interface.

Authors:  Xueyan Zhao; Roy David Magnuson
Journal:  J Bacteriol       Date:  2005-03       Impact factor: 3.490

6.  Mutagenic dissection of the sequence determinants of protein folding, recognition, and machine function.

Authors:  Robert T Sauer
Journal:  Protein Sci       Date:  2013-09-18       Impact factor: 6.725

7.  Hybrid incompatibility arises in a sequence-based bioenergetic model of transcription factor binding.

Authors:  Alexander Y Tulchinsky; Norman A Johnson; Ward B Watt; Adam H Porter
Journal:  Genetics       Date:  2014-08-29       Impact factor: 4.562

8.  Quantitative analysis of EGR proteins binding to DNA: assessing additivity in both the binding site and the protein.

Authors:  Jiajian Liu; Gary D Stormo
Journal:  BMC Bioinformatics       Date:  2005-07-13       Impact factor: 3.169

9.  Specificity of Mnt 'master residue' obtained from in vivo and in vitro selections.

Authors:  Fauzi S Silbaq; Steven E Ruttenberg; Gary D Stormo
Journal:  Nucleic Acids Res       Date:  2002-12-15       Impact factor: 16.971

10.  Combinatorial targeting of ribbon-helix-helix artificial transcription factors to chimeric recognition sites.

Authors:  Massimiliano Zampini; Finbarr Hayes
Journal:  Nucleic Acids Res       Date:  2012-04-09       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.