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      p38-MK2 signaling axis regulates RNA metabolism after UV-light-induced DNA damage

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          Abstract

          Ultraviolet (UV) light radiation induces the formation of bulky photoproducts in the DNA that globally affect transcription and splicing. However, the signaling pathways and mechanisms that link UV-light-induced DNA damage to changes in RNA metabolism remain poorly understood. Here we employ quantitative phosphoproteomics and protein kinase inhibition to provide a systems view on protein phosphorylation patterns induced by UV light and uncover the dependencies of phosphorylation events on the canonical DNA damage signaling by ATM/ATR and the p38 MAP kinase pathway. We identify RNA-binding proteins as primary substrates and 14-3-3 as direct readers of p38-MK2-dependent phosphorylation induced by UV light. Mechanistically, we show that MK2 phosphorylates the RNA-binding subunit of the NELF complex NELFE on Serine 115. NELFE phosphorylation promotes the recruitment of 14-3-3 and rapid dissociation of the NELF complex from chromatin, which is accompanied by RNA polymerase II elongation.

          Abstract

          UV-light-induced DNA damage affects RNA metabolism but the underlying signalling pathways are largely unexplored. Here, the authors show that UV light triggers p38-MK2-mediated phosphorylation of the NELF complex, promoting its release from chromatin and concurrent transcriptional elongation.

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          The Proteomics Identifications (PRIDE) database and associated tools: status in 2013

          The PRoteomics IDEntifications (PRIDE, http://www.ebi.ac.uk/pride) database at the European Bioinformatics Institute is one of the most prominent data repositories of mass spectrometry (MS)-based proteomics data. Here, we summarize recent developments in the PRIDE database and related tools. First, we provide up-to-date statistics in data content, splitting the figures by groups of organisms and species, including peptide and protein identifications, and post-translational modifications. We then describe the tools that are part of the PRIDE submission pipeline, especially the recently developed PRIDE Converter 2 (new submission tool) and PRIDE Inspector (visualization and analysis tool). We also give an update about the integration of PRIDE with other MS proteomics resources in the context of the ProteomeXchange consortium. Finally, we briefly review the quality control efforts that are ongoing at present and outline our future plans.
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            Promoter-proximal pausing of RNA polymerase II: emerging roles in metazoans.

            Recent years have witnessed a sea change in our understanding of transcription regulation: whereas traditional models focused solely on the events that brought RNA polymerase II (Pol II) to a gene promoter to initiate RNA synthesis, emerging evidence points to the pausing of Pol II during early elongation as a widespread regulatory mechanism in higher eukaryotes. Current data indicate that pausing is particularly enriched at genes in signal-responsive pathways. Here the evidence for pausing of Pol II from recent high-throughput studies will be discussed, as well as the potential interconnected functions of promoter-proximally paused Pol II.
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              Getting up to speed with transcription elongation by RNA polymerase II.

              Recent advances in sequencing techniques that measure nascent transcripts and that reveal the positioning of RNA polymerase II (Pol II) have shown that the pausing of Pol II in promoter-proximal regions and its release to initiate a phase of productive elongation are key steps in transcription regulation. Moreover, after the release of Pol II from the promoter-proximal region, elongation rates are highly dynamic throughout the transcription of a gene, and vary on a gene-by-gene basis. Interestingly, Pol II elongation rates affect co-transcriptional processes such as splicing, termination and genome stability. Increasing numbers of factors and regulatory mechanisms have been associated with the steps of transcription elongation by Pol II, revealing that elongation is a highly complex process. Elongation is thus now recognized as a key phase in the regulation of transcription by Pol II.
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                Author and article information

                Contributors
                p.beli@imb-mainz.de
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                9 March 2018
                9 March 2018
                2018
                : 9
                : 1017
                Affiliations
                [1 ]ISNI 0000 0004 1794 1771, GRID grid.424631.6, Institute of Molecular Biology (IMB), ; Ackermannweg 4, 55128 Mainz, Germany
                [2 ]ISNI 0000 0001 0674 042X, GRID grid.5254.6, Cellular Stress Signaling Group, Department of Cellular and Molecular Medicine, Center for Healthy Aging, , University of Copenhagen, ; Blegdamsvej 3C, 2200 Copenhagen, Denmark
                [3 ]ISNI 0000 0001 0674 042X, GRID grid.5254.6, Ubiquitin Signaling Group, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, , University of Copenhagen, ; Blegdamsvej 3B, 2200 Copenhagen, Denmark
                [4 ]ISNI 0000 0001 0674 042X, GRID grid.5254.6, Proteomics and Cell Signaling Group, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, , University of Copenhagen, ; Blegdamsvej 3B, 2200 Copenhagen, Denmark
                [5 ]ISNI 0000 0004 1936 9721, GRID grid.7839.5, Institute of Biochemistry II, Goethe University Medical School, Theodor-Stern-Kai 7, 60590 Frankfurt and Buchmann Institute for Molecular Life Sciences (BMLS), , Goethe University, ; Max-von Laue-Strasse 15, 60438 Frankfurt, Germany
                [6 ]ISNI 0000 0004 1936 9721, GRID grid.7839.5, Department of Medicine, Hematology/Oncology, , Goethe University, ; Theodor-Stern-Kai 7, 60590 Frankfurt, Germany
                [7 ]ISNI 0000 0004 0492 0584, GRID grid.7497.d, German Cancer Consortium (DKTK), ; 69120 Heidelberg, Germany
                [8 ]ISNI 0000 0004 0492 0584, GRID grid.7497.d, German Cancer Research Center (DKFZ), ; 69120 Heidelberg, Germany
                Author information
                http://orcid.org/0000-0002-6623-709X
                http://orcid.org/0000-0002-8629-6310
                http://orcid.org/0000-0001-9507-9820
                Article
                3417
                10.1038/s41467-018-03417-3
                5845016
                29523821
                2c4951e5-26c4-4e36-9d6b-f76d7c71713e
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 3 September 2017
                : 9 February 2018
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