Evidence map›Paper›PMID 31296950›Full record

ArticleScientific reports2019

PARP1 regulates DNA damage-induced nucleolar-nucleoplasmic shuttling of WRN and XRCC1 in a toxicant and protein-specific manner.

Sebastian Veith, Andrea Schink, Marina Engbrecht, Matthias Mack, Lisa Rank, Pascal Rossatti, Mariam Hakobyan, Denise Goly, Tanja Hefele, Marco Frensch and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 34 citations in OpenAlex.

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  20. Nuclear Organization in Response to Stress: A Special Focus on Nucleoli.Results and problems in cell differentiation · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Sebastian VeithMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Andrea SchinkMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Marina EngbrechtMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Matthias MackMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Lisa RankMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Pascal RossattiMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Mariam HakobyanMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Denise GolyMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Tanja HefeleMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Marco FrenschMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Arthur FischbachMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Alexander BürkleMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany.
Aswin MangerichMolecular Toxicology Group, Department of Biology, University of Konstanz, Konstanz, Germany. aswin.mangerich@uni-konstanz.de.ORCID http://orcid.org/0000-0001-9742-2338
University of Konstanz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prime function of nucleoli is ribogenesis, however, several other, non-canonical functions have recently been identified, including a role in genotoxic stress response. Upon DNA damage, numerous proteins shuttle dynamically between the nucleolus and the nucleoplasm, yet the underlying molecular mechanisms are incompletely understood. Here, we demonstrate that PARP1 and PARylation contribute to genotoxic stress-induced nucleolar-nucleoplasmic shuttling of key genome maintenance factors in HeLa cells. Our work revealed that the RECQ helicase, WRN, translocates from nucleoli to the nucleoplasm upon treatment with the oxidizing agent H

Indexed as

CamptothecinCell NucleolusCell NucleusDNA DamageGossypolHeLa CellsHumansHydrogen PeroxideMustard GasPoly (ADP-Ribose) Polymerase-1Protein BindingProtein TransportWerner Syndrome HelicaseX-ray Repair Cross Complementing Protein 12-chloroethyl ethyl sulfideCamptothecinGossypolHydrogen PeroxideMustard GasPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Werner Syndrome HelicaseWRN protein, humanX-ray Repair Cross Complementing Protein 1XRCC1 protein, human

Identifiers

PMID31296950
PMCPMC6624289
OpenAlexW2961196755

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.