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Dual-initiation promoters with intertwined canonical and TCT/TOP transcription start sites diversify transcript processing
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DualInitiatonPromotersWithIntertwinedCanonical.pdf | Published version | 2.43 MB | Adobe PDF | View/Open |
Title: | Dual-initiation promoters with intertwined canonical and TCT/TOP transcription start sites diversify transcript processing |
Authors: | Nepal, C Hadzhiev, Y Balwierz, P Tarifeño-Saldivia, E Cardenas, R Wragg, JW Suzuki, A-M Carninci, P Peers, B Lenhard, B Andersen, JB Müller, F |
Item Type: | Journal Article |
Abstract: | Variations in transcription start site (TSS) selection reflect diversity of preinitiation complexes and can impact on post-transcriptional RNA fates. Most metazoan polymerase II-transcribed genes carry canonical initiation with pyrimidine/purine (YR) dinucleotide, while translation machinery-associated genes carry polypyrimidine initiator (5'-TOP or TCT). By addressing the developmental regulation of TSS selection in zebrafish we uncovered a class of dual-initiation promoters in thousands of genes, including snoRNA host genes. 5'-TOP/TCT initiation is intertwined with canonical initiation and used divergently in hundreds of dual-initiation promoters during maternal to zygotic transition. Dual-initiation in snoRNA host genes selectively generates host and snoRNA with often different spatio-temporal expression. Dual-initiation promoters are pervasive in human and fruit fly, reflecting evolutionary conservation. We propose that dual-initiation on shared promoters represents a composite promoter architecture, which can function both coordinately and divergently to diversify RNAs. |
Issue Date: | 10-Jan-2020 |
Date of Acceptance: | 19-Nov-2019 |
URI: | http://hdl.handle.net/10044/1/76236 |
DOI: | 10.1038/s41467-019-13687-0 |
ISSN: | 2041-1723 |
Publisher: | Nature Research (part of Springer Nature) |
Journal / Book Title: | Nature Communications |
Volume: | 11 |
Issue: | 1 |
Copyright Statement: | © Crown 2020. This article is licensed under a Creative CommonsAttribution 4.0 International License, which permits use, sharing,adaptation, distribution and reproduction in any medium or format, as long as you giveappropriate credit to the original author(s) and the source, provide a link to the CreativeCommons license, and indicate if changes were made. The images or other third partymaterial in this article are included in the article’s Creative Commons license, unlessindicated otherwise in a credit line to the material. If material is not included in thearticle’s Creative Commons license and your intended use is not permitted by statutoryregulation or exceeds the permitted use, you will need to obtain permission directly fromthe copyright holder. To view a copy of this license, visithttp://creativecommons.org/licenses/by/4.0/. |
Publication Status: | Published |
Conference Place: | England |
Article Number: | ARTN 168 |
Appears in Collections: | Institute of Clinical Sciences |