Shirvani Shervin M, Mookanamparambil Linette, Ramoni Marco F, Chin Michael T
Vascular Medicine Research, Cardiovascular Division, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Physiol Genomics. 2007 Jun 19;30(1):61-8. doi: 10.1152/physiolgenomics.00277.2006. Epub 2007 Feb 27.
The cardiovascular restricted transcription factor CHF1/Hey2 has been previously shown to regulate the smooth muscle response to growth factors. To determine how CHF1/Hey2 affects the smooth muscle response to growth factors, we performed a genomic screen for transcripts that are differentially expressed in wild-type and knockout smooth muscle cells after stimulation with platelet-derived growth factor. We screened 45,101 probes representing >39,000 transcripts derived from at least 34,000 genes, at eight different time points. We analyzed the expression data utilizing an algorithm based on Bayesian statistics to derive the best polynomial clustering model to fit the expression data. We found that in a total of 9,827 transcripts the normalized ratio of knockout to wild-type expression diverged more than threefold from baseline in at least one time point, and these transcripts separated into 17 distinct clusters. Further analysis of each cluster revealed distinct alterations in gene expression patterns for immediate early genes, transcription factors, matrix metalloproteinases, signaling molecules, and other molecules important in vascular biology. Our findings demonstrate that CHF1/Hey2 profoundly affects vascular smooth muscle phenotype by altering both the absolute expression level of a variety of genes and the kinetics of growth factor-induced gene expression.
心血管限制性转录因子CHF1/Hey2先前已被证明可调节平滑肌对生长因子的反应。为了确定CHF1/Hey2如何影响平滑肌对生长因子的反应,我们进行了一项基因组筛选,以寻找在血小板衍生生长因子刺激后野生型和基因敲除平滑肌细胞中差异表达的转录本。我们在八个不同时间点筛选了代表至少34,000个基因的>39,000个转录本的45,101个探针。我们利用基于贝叶斯统计的算法分析表达数据,以得出最适合表达数据的最佳多项式聚类模型。我们发现,在总共9,827个转录本中,基因敲除与野生型表达的标准化比率在至少一个时间点与基线的差异超过三倍,并且这些转录本分为17个不同的簇。对每个簇的进一步分析揭示了立即早期基因、转录因子、基质金属蛋白酶、信号分子和血管生物学中其他重要分子的基因表达模式的明显改变。我们的研究结果表明,CHF1/Hey2通过改变多种基因的绝对表达水平和生长因子诱导的基因表达动力学,深刻影响血管平滑肌表型。