Contribution of serum response factor and myocardin to transcriptional regulation of smoothelins

Cardiovasc Res. 2006 Apr 1;70(1):136-45. doi: 10.1016/j.cardiores.2005.12.018. Epub 2006 Jan 31.

Abstract

Objective: Smoothelin-A and -B isoforms are highly restricted to contractile smooth muscle cells (SMCs). Serum response factor (SRF) and myocardin are essential for contractile SMC differentiation. We evaluated the contribution of SRF/myocardin to transcriptional regulation of smoothelins.

Methods: Rat vascular SMCs were transfected with smoothelin-A and smoothelin-B promoter reporter constructs and promoter activity was analyzed. The effects of mutations in the smoothelin-A promoter CArG-boxes and co-transfections with a myocardin expression plasmid were assessed. Electrophoretic mobility shift assays and chromatin immunoprecipitations were performed to investigate SRF-binding to the smoothelin-A CArG-boxes.

Results: Smoothelin promoter activity was detected in vascular SMCs. Comparative sequence analysis revealed two conserved CArG elements in the smoothelin-A promoter that bind SRF as shown by chromatin immunoprecipitation. The proximal CArG-near bound SRF stronger than CArG-far in gel shift assays. Mutagenesis studies also indicated that CArG-near is more important than CArG-far in regulating smoothelin-A promoter activity. Myocardin augmented smoothelin-A promoter activity 2.5-fold in a CArG-near-dependent manner. In contrast, myocardin had little effect on the smoothelin-B promoter.

Conclusion: Smoothelin-A expression is controlled by an intragenic promoter whose activity is, in part, dependent on two CArG boxes that bind SRF. Our data show a role for SRF/myocardin in regulating smoothelin-A whereas the higher smoothelin-B expression appears to be SRF/myocardin-independent.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cells, Cultured
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism*
  • Electrophoretic Mobility Shift Assay / methods
  • Gene Expression
  • Gene Expression Regulation*
  • Humans
  • Immunoprecipitation / methods
  • Mice
  • Molecular Sequence Data
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Myocytes, Smooth Muscle / metabolism*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic*
  • Protein Binding
  • RNA, Messenger / analysis
  • Rats
  • Sequence Analysis, DNA
  • Serum Response Factor / genetics
  • Serum Response Factor / immunology
  • Serum Response Factor / metabolism*
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcription, Genetic

Substances

  • Cytoskeletal Proteins
  • Muscle Proteins
  • Nuclear Proteins
  • RNA, Messenger
  • Serum Response Factor
  • Smtn protein, rat
  • Trans-Activators
  • myocardin