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

    • 1The Gurdon Institute, and Department of Genetics, University of Cambridge, Cambridge CB3 0DH, United Kingdom;
    • 2Department of Biology, Carolina Center for Genome Sciences, and Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3280, USA;
    • 3Department of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California 95060, USA;
    • 4Department of Genetics and Genome Sequencing Center, Washington University School of Medicine, St. Louis, Missouri 63108, USA
    • 5 These authors contributed equally to this work.
    • 6 Corresponding author Email [email protected]
Published April 2, 2013. https://doi.org/10.1101/gr.153668.112
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cover of Genome Research Vol 36 Issue 6
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Abstract

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.

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