Binding of Serum Response Factor to CArG Box Sequences Is Necessary but Not Sufficient to Restrict Gene Expression to Arterial Smooth Muscle Cells

• Published in: The Journal of biological chemistry 2001-05, Vol.276 (19), p.16418-16424
• Main Authors: Strobeck, Mark, Kim, Steven, Zhang, Janet C.L., Clendenin, Cynthia, Du, Kevin L., Parmacek, Michael S.
• Format: Article
• Language: English
• Subjects: 3' Untranslated Regions - genetics; 3T3 Cells; 5' Untranslated Regions - genetics; Animals; Aorta; Arteries - embryology; Base Sequence; beta-Galactosidase - genetics; Binding Sites; Cell Line; Cells, Cultured; DNA-Binding Proteins - metabolism; Gene Expression Regulation; Genes, fos; Heart - embryology; HeLa Cells; Humans; Mice; Mice, Transgenic; Microfilament Proteins - genetics; Molecular Sequence Data; Muscle Proteins - genetics; Muscle, Smooth, Vascular - cytology; Muscle, Smooth, Vascular - physiology; Nuclear Proteins - metabolism; Promoter Regions, Genetic; Rats; Sequence Deletion; Serum Response Factor; Transcription Factors - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M100631200

Serum response factor (SRF) plays an important role in regulating smooth muscle cell (SMC) development and differentiation. To understand the molecular mechanisms underlying the activity of SRF in SMCs, the two CArG box-containing elements in the arterial SMC-specific SM22α promoter, SME-1 and SME-4, were functionally and biochemically characterized. Mutations that abolish binding of SRF to the SM22α promoter totally abolish promoter activity in transgenic mice. Moreover, a multimerized copy of either SME-1 or SME-4 subcloned 5′ of the minimal SM22α promoter (base pairs −90 to +41) is necessary and sufficient to restrict transgene expression to arterial SMCs in transgenic mice. In contrast, a multimerized copy of the c-fos SRE is totally inactive in arterial SMCs and substitution of the c-fos SRE for the CArG motifs within the SM22α promoter inactivates the 441-base pair SM22α promoter in transgenic mice. Deletion analysis revealed that the SME-4 CArG box alone is insufficient to activate transcription in SMCs and additional 5′-flanking nucleotides are required. Nuclear protein binding assays revealed that SME-4 binds SRF, YY1, and four additional SMC nuclear proteins. Taken together, these data demonstrate that binding of SRF to specific CArG boxes is necessary, but not sufficient, to restrict transgene expression to SMCs in vivo.