Lymphocyte Cell Biology Section, Molecular Immunology and Inflammation Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892-1930, USA.
Cell. 2012 Nov 21;151(5):981-93. doi: 10.1016/j.cell.2012.09.044.
Signaling pathways are intimately involved in cellular differentiation, allowing cells to respond to their environment by regulating gene expression. Although enhancers are recognized as key elements that regulate selective gene expression, the interplay between signaling pathways and actively used enhancer elements is not clear. Here, we use CD4(+) T cells as a model of differentiation, mapping the activity of cell-type-specific enhancer elements in T helper 1 (Th1) and Th2 cells. Our data establish that STAT proteins have a major impact on the activation of lineage-specific enhancers and the suppression of enhancers associated with alternative cell fates. Transcriptome analysis further supports a functional role for enhancers regulated by STATs. Importantly, expression of lineage-defining master regulators in STAT-deficient cells fails to fully recover the chromatin signature of STAT-dependent enhancers. Thus, these findings point to a critical role of STATs as environmental sensors in dynamically molding the specialized enhancer architecture of differentiating cells.
信号通路与细胞分化密切相关,使细胞能够通过调节基因表达来响应其环境。尽管增强子被认为是调节选择性基因表达的关键元件,但信号通路与活跃使用的增强子元件之间的相互作用尚不清楚。在这里,我们以 CD4(+)T 细胞作为分化模型,绘制了 T 辅助 1(Th1)和 Th2 细胞中细胞类型特异性增强子元件的活性。我们的数据表明,STAT 蛋白对谱系特异性增强子的激活和对与替代细胞命运相关的增强子的抑制有重大影响。转录组分析进一步支持了由 STAT 调节的增强子的功能作用。重要的是,STAT 缺陷细胞中谱系定义的主调控因子的表达未能完全恢复 STAT 依赖性增强子的染色质特征。因此,这些发现表明 STAT 作为环境传感器在动态塑造分化细胞的特化增强子结构方面起着关键作用。