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PMID: 8632009 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

DNA binding specificity of the CCAAT/enhancer-binding protein transcription factor family.

The Journal of biological chemistry ·Vol. 271 ·No. 7 ·1996-02-16 ·Pages 3891-6

Osada S, Yamamoto H, Nishihara T, Imagawa M

Abstract

CCAAT/enhancer-binding protein (C/EBP) transcription factor family members are related by a high degree of amino acid sequence identity to the basic leucine zipper DNA-binding domain and show distinct but overlapping patterns of tissue- and stage-restricted expression. Although C/EBPalpha and C/EBPbeta have been shown to recognize a consensus sequence derived from regulatory elements in virus and acute-phase response genes, the potential for more subtle differences in the binding preference of the C/EBP family has not been previously addressed. The consensus sequence of C/EBPdelta has not been reported. By using the method of polymerase chain reaction-mediated random site selection to assess the DNA binding specificity of the C/EBP family in an unbiased manner, we demonstrated the sequence preferences for C/EBP family members. With small variations, these C/EBP family members showed similar sequence preferences, and the consensus sequence was identified as RTTGCGYAAY (R = A or G, and Y = C or T). The phosphorylation of C/EBPdelta by casein kinase II increased the binding activity, but did not affect the binding specificity, whereas it was reported that the phosphorylation of C/EBPalpha and C/EBPbeta decreased the binding affinity. The specificity of action of C/EBP family members may be derived from the characteristics of each factor, including the expression profiles, the DNA binding affinities, the cofactors, and so on, in addition to the DNA binding specificities.

MeSH Terms
Animals Base Sequence Binding Sites Binding, Competitive CCAAT-Enhancer-Binding Proteins Cloning, Molecular Consensus Sequence DNA/metabolism DNA Primers DNA-Binding Proteins/isolation & purification,metabolism Escherichia coli Kinetics Molecular Sequence Data Nuclear Proteins/isolation & purification,metabolism Polymerase Chain Reaction Recombinant Fusion Proteins/isolation & purification,metabolism Substrate Specificity Transcription Factors/isolation & purification,metabolism
Chemicals
CCAAT-Enhancer-Binding Proteins DNA Primers DNA-Binding Proteins Nuclear Proteins Recombinant Fusion Proteins Transcription Factors DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Osada S
Department of Environmental Biochemistry, Faculty of Pharmaceutical Sciences, Osaka University, 1-6 Yamada-Oka, Suita, Osaka 565, Japan.
Yamamoto H
Nishihara T
Imagawa M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1996-02-16
Pages
3891-6
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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