RNA Biology Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD, 21702, USA.
Genome Analysis Unit, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Nat Commun. 2021 Feb 10;12(1):906. doi: 10.1038/s41467-021-21150-2.
Promoter-proximal pausing regulates eukaryotic gene expression and serves as checkpoints to assemble elongation/splicing machinery. Little is known how broadly this type of pausing regulates transcription in bacteria. We apply nascent elongating transcript sequencing combined with RNase I footprinting for genome-wide analysis of σ-dependent transcription pauses in Escherichia coli. Retention of σ induces strong backtracked pauses at a 10-20-bp distance from many promoters. The pauses in the 10-15-bp register of the promoter are dictated by the canonical -10 element, 6-7 nt spacer and "YRY" motif centered at the transcription start site. The promoters for the pauses in the 16-20-bp register contain an additional -10-like sequence recognized by σ. Our in vitro analysis reveals that DNA scrunching is involved in these pauses relieved by Gre cleavage factors. The genes coding for transcription factors are enriched in these pauses, suggesting that σ and Gre proteins regulate transcription in response to changing environmental cues.
启动子近端暂停调节真核基因表达,并作为组装延伸/剪接机制的检查点。目前尚不清楚这种类型的暂停在细菌中是如何广泛调节转录的。我们应用新生延伸转录测序结合 RNase I 足迹法,对大肠杆菌中依赖 σ 的转录暂停进行全基因组分析。σ 的保留会在许多启动子附近 10-20bp 的距离处诱导强烈的回溯暂停。启动子中 10-15bp 寄存器中的暂停由规范的-10 元件、6-7nt 间隔和以转录起始位点为中心的“YRY”基序决定。暂停在 16-20bp 寄存器中的启动子包含 σ 识别的额外的-10 样序列。我们的体外分析表明,DNA 卷曲参与了由 Gre 切割因子缓解的这些暂停。编码转录因子的基因在这些暂停中富集,表明 σ 和 Gre 蛋白根据环境变化调节转录。