Evidence map›Paper›PMID 34108663›Full record

ArticleNature cell biology2021

ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylation.

Yana van der Weegen, Klaas de Lint, Diana van den Heuvel, Yuka Nakazawa, Tycho E T Mevissen, Janne J M van Schie, Marta San Martin Alonso, Daphne E C Boer, Román González-Prieto, Ishwarya V Narayanan and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

66 citing papers in PubMed, 104 citations in OpenAlex.

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6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 5 institutions in 3 countries.

Yana van der Weegen *Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Klaas de Lint *Department of Clinical Genetics, Section Oncogenetics, Cancer Center Amsterdam, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Diana van den HeuvelDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Yuka NakazawaDepartment of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Nagoya, Japan.
Tycho E T MevissenHoward Hughes Medical Institute and Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-2324-5292
Janne J M van SchieDepartment of Clinical Genetics, Section Oncogenetics, Cancer Center Amsterdam, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Marta San Martin AlonsoDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Daphne E C BoerDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Román González-PrietoDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-8997-2321
Ishwarya V NarayananDepartment of Radiation Oncology, University of Michigan, Ann Arbor, MI, USA.
Noud H M KlaassenDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Annelotte P WondergemDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Khashayar RoohollahiDepartment of Clinical Genetics, Section Oncogenetics, Cancer Center Amsterdam, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Josephine C DorsmanDepartment of Clinical Genetics, Section Oncogenetics, Cancer Center Amsterdam, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Yuichiro HaraDepartment of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Nagoya, Japan.
Alfred C O VertegaalDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, The Netherlands.
Job de LangeDepartment of Clinical Genetics, Section Oncogenetics, Cancer Center Amsterdam, Amsterdam University Medical Center, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-9002-8829
Johannes C WalterHoward Hughes Medical Institute and Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-4186-7570
Sylvie M NoordermeerDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0003-2737-9690
Mats LjungmanDepartment of Radiation Oncology, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-1553-6695
Tomoo OgiDepartment of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Nagoya, Japan.ORCID http://orcid.org/0000-0002-5492-9072
Rob M F WolthuisDepartment of Clinical Genetics, Section Oncogenetics, Cancer Center Amsterdam, Amsterdam University Medical Center, Amsterdam, The Netherlands. r.wolthuis@amsterdamumc.nl.ORCID http://orcid.org/0000-0002-3109-1588
Martijn S LuijsterburgDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands. m.luijsterburg@lumc.nl.ORCID http://orcid.org/0000-0001-5796-6541
Leiden University Medical Center · NLNagoya University · JPHoward Hughes Medical Institute · USUniversity of Michigan · USUniversity of Amsterdam · NL

Funding

The Fanconi anemia pathway: role in DNA interstrand cross-link repairR01HL098316 · NHLBI · HARVARD MEDICAL SCHOOL · PI Johannes Walter · 2010 to 2026
$6.3M
Targeting the RNA Exosome for Cancer TherapeuticsR01CA213214 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LJUNGMAN, MATS, NEAMATI, NOURI · 2019 to 2023
$2.4M
Mapping of Novel Candidate Functional Elements with Bru-Seq TechnologyUM1HG009382 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LJUNGMAN, MATS · 2017 to 2021
$2.3M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA213214NHGRI NIH HHS UM1 HG009382NHLBI NIH HHS R01 HL098316
6 · The paper itself

Abstract

Cells employ transcription-coupled repair (TCR) to eliminate transcription-blocking DNA lesions. DNA damage-induced binding of the TCR-specific repair factor CSB to RNA polymerase II (RNAPII) triggers RNAPII ubiquitylation of a single lysine (K1268) by the CRL4

Indexed as

DNA DamageDNA RepairUbiquitinationCell Line, TumorCRISPR-Cas SystemsDNA HelicasesDNA Repair EnzymesHumansPeptide Elongation Factor 1Poly-ADP-Ribose Binding ProteinsProtein BindingProtein Interaction Domains and MotifsReceptors, Interleukin-17RNA Polymerase IITranscription Elongation, GeneticTranscription FactorsDNA HelicasesDNA Repair EnzymesERCC6 protein, humanERCC8 protein, humanIL17RB protein, humanPeptide Elongation Factor 1Poly-ADP-Ribose Binding ProteinsReceptors, Interleukin-17RNA Polymerase IITranscription FactorsUbiquitin-Protein Ligases

Identifiers

PMID34108663
PMCPMC8890769
OpenAlexW3170184056

What OpenQuestion holds

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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.