Evidence map›Paper›PMID 29523821›Full record

ArticleNature communications2018

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

Marina E Borisova, Andrea Voigt, Maxim A X Tollenaere, Sanjeeb Kumar Sahu, Thomas Juretschke, Nastasja Kreim, Niels Mailand, Chunaram Choudhary, Simon Bekker-Jensen, Masato Akutsu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.5field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 83 citations in OpenAlex.

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  20. PAHSAs reduce cellular senescence and protect pancreatic beta cells from metabolic stress through regulation of Mdm2/p53.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Marina E BorisovaInstitute of Molecular Biology (IMB), Ackermannweg 4, 55128, Mainz, Germany.
Andrea VoigtInstitute of Molecular Biology (IMB), Ackermannweg 4, 55128, Mainz, Germany.
Maxim A X TollenaereCellular Stress Signaling Group, Department of Cellular and Molecular Medicine, Center for Healthy Aging, University of Copenhagen, Blegdamsvej 3C, 2200, Copenhagen, Denmark.
Sanjeeb Kumar SahuInstitute of Molecular Biology (IMB), Ackermannweg 4, 55128, Mainz, Germany.
Thomas JuretschkeInstitute of Molecular Biology (IMB), Ackermannweg 4, 55128, Mainz, Germany.
Nastasja KreimInstitute of Molecular Biology (IMB), Ackermannweg 4, 55128, Mainz, Germany.
Niels MailandUbiquitin Signaling Group, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-6623-709X
Chunaram ChoudharyProteomics 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.
Simon Bekker-JensenCellular Stress Signaling Group, Department of Cellular and Molecular Medicine, Center for Healthy Aging, University of Copenhagen, Blegdamsvej 3C, 2200, Copenhagen, Denmark.
Masato AkutsuInstitute 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.
Sebastian A WagnerDepartment of Medicine, Hematology/Oncology, Goethe University, Theodor-Stern-Kai 7, 60590, Frankfurt, Germany.ORCID http://orcid.org/0000-0002-8629-6310
Petra BeliInstitute of Molecular Biology (IMB), Ackermannweg 4, 55128, Mainz, Germany. p.beli@imb-mainz.de.ORCID http://orcid.org/0000-0001-9507-9820
Institute of Molecular Biology · DEUniversity of Copenhagen · DKGoethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

14-3-3 ProteinsAtaxia Telangiectasia Mutated ProteinsCell Line, TumorChromatinDNA-Binding ProteinsDNA DamageHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsMAP-Kinase-Activated Kinase 2p38 Mitogen-Activated Protein KinasesPhosphorylationProtein Serine-Threonine KinasesRNARNA-Binding ProteinsRNA Polymerase II14-3-3 ProteinsAtaxia Telangiectasia Mutated ProteinsATM protein, humanATR protein, humanChromatinDNA-Binding ProteinsIntracellular Signaling Peptides and ProteinsMAP-Kinase-Activated Kinase 2negative elongation factorp38 Mitogen-Activated Protein KinasesProtein Serine-Threonine KinasesRNARNA-Binding ProteinsRNA Polymerase IITranscription Factors

Identifiers

PMID29523821
PMCPMC5845016
OpenAlexW2787843491

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.