Laboratory of Genetics and Physiology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Nucleic Acids Res. 2012 May;40(10):4461-72. doi: 10.1093/nar/gks056. Epub 2012 Feb 8.
Signal Transducers and Activators of Transcription (STAT) 5A/B regulate cytokine-inducible genes upon binding to GAS motifs. It is not known what percentage of genes with GAS motifs bind to and are regulated by STAT5. Moreover, it is not clear whether genome-wide STAT5 binding is modulated by its concentration. To clarify these issues we established genome-wide STAT5 binding upon growth hormone (GH) stimulation of wild-type (WT) mouse embryonic fibroblasts (MEFs) and MEFs overexpressing STAT5A more than 20-fold. Upon GH stimulation, 23 827 and 111 939 STAT5A binding sites were detected in WT and STAT5A overexpressing MEFs, respectively. 13 278 and 71 561 peaks contained at least one GAS motif. 1586 and 8613 binding sites were located within 2.5 kb of promoter sequences, respectively. Stringent filtering revealed 78 genes in which the promoter/upstream region (-10 kb to +0.5 kb) was recognized by STAT5 both in WT and STAT5 overexpressing MEFs and 347 genes that bound STAT5 only in overexpressing cells. Genome-wide expression analyses identified that the majority of STAT5-bound genes was not under GH control. Up to 40% of STAT5-bound genes were not expressed. For the first time we demonstrate the magnitude of opportunistic genomic STAT5 binding that does not translate into transcriptional activation of neighboring genes.
信号转导子和转录激活子(STAT)5A/B 在与 GAS 基序结合后调节细胞因子诱导的基因。目前尚不清楚有多少具有 GAS 基序的基因与 STAT5 结合并受其调节。此外,尚不清楚基因组范围内 STAT5 结合是否受其浓度的调节。为了阐明这些问题,我们建立了生长激素(GH)刺激野生型(WT)小鼠胚胎成纤维细胞(MEF)和 STAT5A 过表达超过 20 倍的 MEF 时的全基因组 STAT5 结合。在 GH 刺激后,WT 和 STAT5A 过表达 MEF 中分别检测到 23827 和 111939 个 STAT5A 结合位点。13278 和 71561 个峰包含至少一个 GAS 基序。分别有 1586 和 8613 个结合位点位于启动子序列的 2.5kb 以内。严格筛选显示,在 WT 和 STAT5A 过表达 MEF 中,有 78 个基因的启动子/上游区域(-10kb 到+0.5kb)被 STAT5 识别,而在过表达细胞中只有 347 个基因结合 STAT5。全基因组表达分析表明,大多数 STAT5 结合基因不受 GH 控制。多达 40%的 STAT5 结合基因不表达。我们首次证明了基因组范围内机会性 STAT5 结合的程度,这种结合不会转化为邻近基因的转录激活。