Abstract

The GATA-4/5/6 family of transcription factors is important for the development of the cardiovascular system and the visceral endoderm. GATA-6 is the only family member expressed in vascular smooth muscle cells and has been shown to be important for controlling the phenotype of these cells following vascular injury. To clarify further the role of GATA-6 in regulating vascular smooth muscle differentiation, we directly examined its ability to regulate the promoters of smooth muscle-specific genes. This analysis revealed that GATA-6 strongly repressed telokin promoter activity. In contrast, GATA-6 activated the smooth muscle myosin heavy chain and smooth muscle alpha-actin promoters and had no significant effect on the SM22alpha promoter. Gel mobility shift assays demonstrate that GATA-6 binds to a consensus site adjacent to the CArG box in the telokin promoter. GATA-6 did not interfere with the serum-response factor-stimulated promoter activity but blocked myocardin-induced activation of the telokin promoter. In contrast, GATA-6 and myocardin resulted in synergistic activation of the smooth muscle myosin heavy chain promoter. Consistent with these findings, overexpression of GATA-6 in smooth muscle cells selectively inhibited expression of endogenous telokin, while simultaneously increasing expression of other smooth muscle proteins. These data suggest that GATA-6 selectively inhibits telokin expression by triggering the displacement of myocardin from the serum-response factor. As GATA-6 is expressed at high levels in vascular smooth muscle, this finding may explain the relatively low levels of telokin expression in the vascular system. These data also reveal a novel transcription regulatory mechanism by which GATA-6 can modulate the activity of the myocardin-serum-response factor complexes.

Highlights

  • Smooth muscle cells arise from diverse populations of precursor cells during embryonic development

  • GATA-6 Selectively Represses the Activity of the Telokin Promoter, While Activating the SM ␣-Actin and smooth muscle myosin heavy chain (Sm-MHC) Promoters—To examine the effect of GATA-6 on smooth muscle-specific promoter activity, GATA-6 expression plasmids were cotransfected into A10 cells together with various reporter plasmids consisting of a firefly luciferase gene driven by SM ␣-actin, Sm-MHC, SM22␣, or telokin promoters

  • We found that GATA-6 selectively repressed telokin promoter activity while activating the Sm-MHC promoter

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Summary

The abbreviations used are

Sm-MHC, smooth muscle myosin heavy chain; SRF, serum response factor; SM, smooth muscle; VSMC, vascular smooth muscle cells; MLCK, myosin light chain kinase. Adenovirus-mediated GATA-6 gene transfer to the vessel wall after balloon injury partially inhibited lesion formation and reversed the down-regulation of Sm-MHC, smooth muscle ␣-actin (SM ␣-actin), calponin, vinculin, and metavinculin expression that is normally associated with injury-induced VSMC phenotypic modulation [32]. These data suggest that GATA-6 plays a critical role in the maintenance of the differentiated phenotype in VSMCs. In the current study, we further investigated the roles of GATA-6 in regulating smooth muscle-specific gene transcription. Together our data reveal a novel transcription regulatory mechanism by which GATA-6 can modulate the activity of myocardin-SRF complexes

EXPERIMENTAL PROCEDURES
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DISCUSSION
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