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The landscape of RNA polymerase II transcription initiation in C. elegans reveals promoter and enhancer architectures

机译:秀丽隐杆线虫RNA聚合酶II转录起始的格局揭示了启动子和增强子的体系结构

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摘要

RNA polymerase transcription initiation sites are largely unknown in Caenorhabditis elegans. The initial 5′ end of most protein-coding transcripts is removed by trans-splicing, and noncoding initiation sites have not been investigated. We characterized the landscape of RNA Pol II transcription initiation, identifying 73,500 distinct clusters of initiation. Bidirectional transcription is frequent, with a peak of transcriptional pairing at 120 bp. We assign transcription initiation sites to 7691 protein-coding genes and find that they display features typical of eukaryotic promoters. Strikingly, the majority of initiation events occur in regions with enhancer-like chromatin signatures. Based on the overlap of transcription initiation clusters with mapped transcription factor binding sites, we define 2361 transcribed intergenic enhancers. Remarkably, productive transcription elongation across these enhancers is predominantly in the same orientation as that of the nearest downstream gene. Directed elongation from an upstream enhancer toward a downstream gene could potentially deliver RNA polymerase II to a proximal promoter, or alternatively might function directly as a distal promoter. Our results provide a new resource to investigate transcription regulation in metazoans.
机译:在秀丽隐杆线虫中,RNA聚合酶转录起始位点很大程度上未知。大多数蛋白质编码转录本的起始5'末端通过反式剪接去除,尚未研究非编码起始位点。我们表征了RNA Pol II转录起始的格局,确定了73,500个不同的起始簇。双向转录非常频繁,转录配对的峰值为120 bp。我们将转录起始位点分配给7691蛋白编码基因,发现它们显示出典型的真核启动子特征。引人注目的是,大多数启动事件发生在具有增强子样染色质特征的区域。基于转录启动簇与映射的转录因子结合位点的重叠,我们定义了2361个转录的基因间增强子。值得注意的是,跨这些增强子的生产性转录延伸主要与最近的下游基因处于相同的方向。从上游增强子向下游基因的定向延伸可潜在地将RNA聚合酶II递送至近端启动子,或可替代地可直接充当远端启动子。我们的结果为研究后生动物的转录调控提供了新的资源。

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