Division of Cardiology, Department of Medicine, University of Washington, Seattle, WA 98109, United States.
Biochem Biophys Res Commun. 2011 Dec 2;415(4):662-8. doi: 10.1016/j.bbrc.2011.10.132. Epub 2011 Nov 3.
The cardiovascular restricted bHLH transcription factor CHF1/Hey2 has been reported to play an important role in regulation of vascular smooth muscle phenotype and gene expression, but the downstream target genes that mediate these effects have not been completely elucidated. We have previously found that loss of CHF1/Hey2 in vascular smooth muscle cells leads to dysregulated expression of the matrix metalloproteinase gene MMP10 after treatment with PDGF. Here we report that loss or knockdown of CHF1/Hey2 in vascular smooth muscle cells leads to increased expression and activity of MMP10 at baseline, suggesting a direct effect of CHF1/Hey2 on MMP10 promoter regulation. To test this hypothesis, we assessed the effects of CHF1/Hey2 on a 2.5 kb MMP10 promoter region upstream of the transcriptional start site. We found that this region contains multiple elements including 12 E-boxes that mediate constitutive activity and repression by CHF1/Hey2 in 293T cells and A7r5 smooth muscle cells. Surprisingly, mutation of these E-boxes not only abolished CHF1/Hey2 repression, but also diminished constitutive expression. In addition, we observed that some of these mutations unmasked an activator function for CHF1/Hey2, which has not been previously described. These findings support the hypothesis that CHF1/Hey2 is an important regulator of MMP10 expression.
心血管受限 bHLH 转录因子 CHF1/Hey2 已被报道在调节血管平滑肌表型和基因表达中发挥重要作用,但介导这些作用的下游靶基因尚未完全阐明。我们之前发现,血管平滑肌细胞中 CHF1/Hey2 的缺失导致 PDGF 处理后基质金属蛋白酶基因 MMP10 的表达失调。在这里,我们报告说,血管平滑肌细胞中 CHF1/Hey2 的缺失或敲低导致 MMP10 的基础表达和活性增加,表明 CHF1/Hey2 对 MMP10 启动子调控有直接影响。为了验证这一假设,我们评估了 CHF1/Hey2 对转录起始位点上游 MMP10 启动子 2.5 kb 区域的影响。我们发现,该区域包含多个元件,包括 12 个 E 盒,在 293T 细胞和 A7r5 平滑肌细胞中介导组成性活性和 CHF1/Hey2 的抑制。令人惊讶的是,这些 E 盒的突变不仅消除了 CHF1/Hey2 的抑制作用,而且还降低了组成性表达。此外,我们观察到这些突变中的一些揭示了 CHF1/Hey2 的激活功能,这以前尚未描述过。这些发现支持了 CHF1/Hey2 是 MMP10 表达的重要调节剂的假说。