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PMID: 9545312 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Enhancement of serum-response factor-dependent transcription and DNA binding by the architectural transcription factor HMG-I(Y).

The Journal of biological chemistry ·Vol. 273 ·No. 16 ·1998-04-17 ·Pages 9755-60

Chin MT, Pellacani A, Wang H, Lin SS, Jain MK, Perrella MA, Lee ME

Abstract

The mechanisms by which HMG-I proteins regulate cell growth are unknown, and their effects on gene expression have only been partially elucidated. We explored the potential interaction between HMG-I proteins and serum-response factor (SRF), a member of the MADS-box family of transcription factors. In cotransfection experiments, HMG-I(Y) potentiated SRF-dependent activation (by more than 5-fold) of two distinct SRF-responsive promoters, c-fos and the smooth muscle-specific gene SM22alpha. This effect was also observed with a heterologous promoter containing multiple copies of the CC(A/T)6GG (CArG) box. HMG-I proteins bound specifically to the CArG boxes of c-fos and SM22alpha in gel mobility shift analysis and enhanced binding of SRF to these CArG boxes. By chelating peptide-immobilized metal affinity chromatography, we mapped the domain of HMG-I(Y) that interacts with SRF to amino acids 50-81, a region that does not bind specifically to DNA in electrophoretic mobility shift assays even though it includes the third AT-hook DNA-binding domain. Surprisingly, HMG-I(Y) mutants that failed to bind DNA still enhanced SRF binding to DNA and SRF-dependent transcription. In contrast, deletion of the HMG-I(Y) 50-81 domain that bound SRF prevented enhancement of transcription. To our knowledge, this is the first report of an HMG-I protein interacting with a MADS-box transcription factor. Our observations suggest that members of the HMG-I family play an important role in SRF-dependent transcription and that their effect is mediated primarily by a protein-protein interaction.

MeSH Terms
Animals Base Sequence Binding Sites Cell Line DNA-Binding Proteins/metabolism Drosophila Genes, fos HMGA1a Protein High Mobility Group Proteins/metabolism Kinetics Microfilament Proteins Molecular Sequence Data Muscle Proteins/biosynthesis Muscle, Smooth/metabolism Nuclear Proteins/metabolism Oligodeoxyribonucleotides Promoter Regions, Genetic Proto-Oncogene Proteins c-fos/biosynthesis Rats Recombinant Proteins/biosynthesis,metabolism Serum Response Factor Transcription Factors/metabolism Transfection
Chemicals
DNA-Binding Proteins High Mobility Group Proteins Microfilament Proteins Muscle Proteins Nuclear Proteins Oligodeoxyribonucleotides Proto-Oncogene Proteins c-fos Recombinant Proteins Serum Response Factor Tagln protein, mouse Transcription Factors transgelin HMGA1a Protein
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Chin M T
Cardiovascular Biology Laboratory, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
Pellacani A
Wang H
Lin S S
Jain M K
Perrella M A
Lee M E
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1998-04-17
Pages
9755-60
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM53249 · United States
NHLBI NIH HHS · HL03194 · United States
NHLBI NIH HHS · HL03745 · United States
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