Evidence map›Paper›PMID 31217442›Full record

ArticleScientific reports2019

Replication fork rescue in mammalian mitochondria.

Rubén Torregrosa-Muñumer, Anu Hangas, Steffi Goffart, Daniel Blei, Gábor Zsurka, Jack Griffith, Wolfram S Kunz, Jaakko L O Pohjoismäki

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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

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  14. International journal of molecular sciences · 2021
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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

8 authors at 4 institutions in 3 countries.

Rubén Torregrosa-MuñumerDepartment of Environmental and Biological Sciences, University of Eastern Finland, P.O. Box 111, 80101, Joensuu, Finland.
Anu HangasDepartment of Environmental and Biological Sciences, University of Eastern Finland, P.O. Box 111, 80101, Joensuu, Finland.
Steffi GoffartDepartment of Environmental and Biological Sciences, University of Eastern Finland, P.O. Box 111, 80101, Joensuu, Finland.
Daniel BleiDepartment of Experimental Epileptology and Cognition Research, University of Bonn, Sigmund-Freud-Str. 25, Bonn, D-53105, Germany.
Gábor ZsurkaDepartment of Experimental Epileptology and Cognition Research, University of Bonn, Sigmund-Freud-Str. 25, Bonn, D-53105, Germany.ORCID http://orcid.org/0000-0002-6379-849X
Jack GriffithLineberger Comprehensive Cancer Center, University of North Carolina at, Chapel Hill, USA.
Wolfram S KunzDepartment of Experimental Epileptology and Cognition Research, University of Bonn, Sigmund-Freud-Str. 25, Bonn, D-53105, Germany.
Jaakko L O PohjoismäkiDepartment of Environmental and Biological Sciences, University of Eastern Finland, P.O. Box 111, 80101, Joensuu, Finland. Jaakko.Pohjoismaki@uef.fi.ORCID http://orcid.org/0000-0002-1185-3610
University of Bonn · DEUniversity of Eastern Finland · FIUniversity of Helsinki · FIUniversity of North Carolina at Chapel Hill · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Replication stalling has been associated with the formation of pathological mitochondrial DNA (mtDNA) rearrangements. Yet, almost nothing is known about the fate of stalled replication intermediates in mitochondria. We show here that replication stalling in mitochondria leads to replication fork regression and mtDNA double-strand breaks. The resulting mtDNA fragments are normally degraded by a mechanism involving the mitochondrial exonuclease MGME1, and the loss of this enzyme results in accumulation of linear and recombining mtDNA species. Additionally, replication stress promotes the initiation of alternative replication origins as an apparent means of rescue by fork convergence. Besides demonstrating an interplay between two major mechanisms rescuing stalled replication forks - mtDNA degradation and homology-dependent repair - our data provide evidence that mitochondria employ similar mechanisms to cope with replication stress as known from other genetic systems.

Indexed as

DNA ReplicationAnimalsDNA Breaks, Double-StrandedDNA, MitochondrialExodeoxyribonucleasesGene DosageHEK293 CellsHumansMammalsMitochondriaStress, PhysiologicalUltraviolet RaysDNA, MitochondrialExodeoxyribonucleasesMGME1 protein, human

Identifiers

PMID31217442
PMCPMC6584726
OpenAlexW2950496620

What OpenQuestion holds

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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.