Molecular Biology Institute, UCLA, Los Angeles, United States.
Department of Microbiology, UCLA, Los Angeles, United States.
Elife. 2021 Mar 11;10:e63512. doi: 10.7554/eLife.63512.
Regulation of RNA polymerase II (Pol2) elongation in the promoter-proximal region is an important and ubiquitous control point for gene expression in metazoans. We report that transcription of the adenovirus 5 E4 region is regulated during the release of paused Pol2 into productive elongation by recruitment of the super-elongation complex, dependent on promoter H3K18/27 acetylation by CBP/p300. We also establish that this is a general transcriptional regulatory mechanism that applies to ~7% of expressed protein-coding genes in primary human airway epithelial cells. We observed that a homeostatic mechanism maintains promoter, but not enhancer, H3K18/27ac in response to extensive inhibition of CBP/p300 acetyl transferase activity by the highly specific small molecule inhibitor A-485. Further, our results suggest a function for BRD4 association at enhancers in regulating paused Pol2 release at nearby promoters. Taken together, our results uncover the processes regulating transcriptional elongation by promoter region histone H3 acetylation and homeostatic maintenance of promoter, but not enhancer, H3K18/27ac in response to inhibition of CBP/p300 acetyl transferase activity.
RNA 聚合酶 II(Pol2)在启动子近端区域的延伸调控是真核生物基因表达的一个重要且普遍的调控点。我们报告说,通过募集超延伸复合物,依赖于 CBP/p300 对启动子 H3K18/27 乙酰化的作用,腺病毒 5 E4 区域的转录在暂停的 Pol2 进入生产性延伸时受到调控。我们还确定,这是一种普遍的转录调控机制,适用于原代人呼吸道上皮细胞中约 7%的表达蛋白编码基因。我们观察到,一种动态平衡机制维持启动子,但不维持增强子的 H3K18/27ac,以响应 CBP/p300 乙酰转移酶活性的高度特异性小分子抑制剂 A-485 的广泛抑制。此外,我们的结果表明,BRD4 与增强子的关联在调节附近启动子上暂停的 Pol2 释放方面具有功能。总之,我们的结果揭示了通过启动子区域组蛋白 H3 乙酰化来调节转录延伸的过程,以及在 CBP/p300 乙酰转移酶活性受到抑制时,维持启动子但不维持增强子 H3K18/27ac 的动态平衡机制。