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PMID: 11438530 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Altering the DNA-binding specificity of the yeast Matalpha 2 homeodomain protein.

The Journal of biological chemistry ·Vol. 276 ·No. 35 ·2001-08-31 ·Pages 32696-703

Mathias JR, Zhong H, Jin Y, Vershon AK

Abstract

Homeodomain proteins are a highly conserved class of DNA-binding proteins that are found in virtually every eukaryotic organism. The conserved mechanism that these proteins use to bind DNA suggests that there may be at least a partial DNA recognition code for this class of proteins. To test this idea, we have investigated the sequence-specific requirements for DNA binding and repression by the yeast alpha2 homeodomain protein in association with its cofactors, Mcm1 and Mata1. We have determined the contribution for each residue in the alpha2 homeodomain that contacts the DNA in the co-crystal structures of the protein. We have also engineered mutants in the alpha2 homeodomain to alter the DNA-binding specificity of the protein. Although we were unable to change the specificity of alpha2 by making substitutions at residues 47, 54, and 55, we were able to alter the DNA-binding specificity by making substitutions at residue 50 in the homeodomain. Since other homeodomain proteins show similar changes in specificity with substitutions at residue 50, this suggests that there is at least a partial DNA recognition code at this position.

MeSH Terms
Amino Acid Substitution Binding Sites Crystallography, X-Ray DNA Probes DNA, Fungal/chemistry,metabolism DNA-Binding Proteins/chemistry,metabolism Fungal Proteins/chemistry,genetics,metabolism Homeodomain Proteins/chemistry,genetics,metabolism Minichromosome Maintenance 1 Protein Mutagenesis, Site-Directed Nucleic Acid Conformation Protein Conformation Protein Structure, Secondary Recombinant Fusion Proteins/metabolism Recombinant Proteins/chemistry,metabolism Repressor Proteins/chemistry,genetics,metabolism Saccharomyces cerevisiae/genetics,metabolism Saccharomyces cerevisiae Proteins Serine Transcription Factors/chemistry,metabolism beta-Galactosidase/genetics,metabolism
Chemicals
DNA Probes DNA, Fungal DNA-Binding Proteins Fungal Proteins Homeodomain Proteins MATA1 protein, S cerevisiae MATA2 protein, S cerevisiae Minichromosome Maintenance 1 Protein Recombinant Fusion Proteins Recombinant Proteins Repressor Proteins Saccharomyces cerevisiae Proteins Transcription Factors Serine beta-Galactosidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Mathias J R
Waksman Institute and the Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, New Jersey 08854-8020, USA.
Zhong H
Jin Y
Vershon A K
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2001-08-31
Epub
2001-00-03
Pages
32696-703
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM49265 · United States
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