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PMID: 1317057 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Acquisition of myogenic specificity by replacement of three amino acid residues from MyoD into E12.

Science (New York, N.Y.) ·Vol. 256 ·No. 5059 ·1992-05-15 ·Pages 1027-30

Davis RL, Weintraub H

Abstract

The basic helix-loop-helix (bHLH) protein MyoD is a transcription factor that is important for the induction of the myogenic phenotype. The DNA binding basic region (13 amino acids) is necessary for recognition of the consensus MyoD binding site, for transcriptional activation, and for conversion of fibroblasts to muscle. In contrast, the non-tissue-specific bHLH protein E12 can bind to the MyoD binding site but does not induce myogenesis. Here, it is shown that only two amino acids in the MyoD basic region and a single amino acid from the junction, which separates the basic region and helix 1, are sufficient for myogenic specificity when substituted into the corresponding region of E12. These findings suggest that the recognition of particular determinants in the basic region is required for conversion of fibroblasts to muscle.

MeSH Terms
Amino Acid Sequence Base Sequence Binding Sites Cell Differentiation Cell Line DNA/metabolism DNA Probes DNA-Binding Proteins/chemistry,metabolism,pharmacology Fibroblasts/cytology Fluorescent Antibody Technique Molecular Sequence Data Muscle Proteins/chemistry,genetics,physiology Muscles/cytology MyoD Protein Protein Conformation Structure-Activity Relationship Transcription Factors/chemistry,metabolism,pharmacology Transfection
Chemicals
DNA Probes DNA-Binding Proteins Muscle Proteins MyoD Protein Transcription Factors DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Davis R L
Howard Hughes Medical Institute Laboratory, Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
Weintraub H
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1992-05-15
Pages
1027-30
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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