Evidence map›Paper›PMID 40324391›Full record

ArticleThe Plant cell2025

R-loop control and mitochondrial genome stability require the 5'-3' exonuclease/flap endonuclease OEX1.

Déborah Schatz, Anaïs Le Blevenec, Fabio G Moratti, Kin Pan Chung, Pierre Mercier, Rana Khalid Iqbal, Elody Vallet, André Dietrich, Ralph Bock, Frédérique Weber-Lotfi and 1 more

Abstract read
In one paragraph

Article in The Plant cell, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

11 authors.

Déborah SchatzCNRS, Institut de Biologie Moléculaire des Plantes, University of Strasbourg, Strasbourg, France.ORCID 0009-0001-7524-5921
Anaïs Le BlevenecCNRS, Institut de Biologie Moléculaire des Plantes, University of Strasbourg, Strasbourg, France.ORCID 0000-0002-7114-9393
Fabio G MorattiDepartment of Organelle Biology, Biotechnology and Molecular Ecophysiology, Max Planck Institute of Molecular Plant Physiology, D-14476 Potsdam-Golm, Germany.ORCID 0000-0002-9492-8840
Kin Pan ChungDepartment of Organelle Biology, Biotechnology and Molecular Ecophysiology, Max Planck Institute of Molecular Plant Physiology, D-14476 Potsdam-Golm, Germany.ORCID 0000-0003-2786-3095
Pierre MercierCNRS, Institut de Biologie Moléculaire des Plantes, University of Strasbourg, Strasbourg, France.
Rana Khalid IqbalCNRS, Institut de Biologie Moléculaire des Plantes, University of Strasbourg, Strasbourg, France.ORCID 0000-0002-5130-8123
Elody ValletCNRS, Institut de Biologie Moléculaire des Plantes, University of Strasbourg, Strasbourg, France.ORCID 0009-0001-7704-0348
André DietrichCNRS, Institut de Biologie Moléculaire des Plantes, University of Strasbourg, Strasbourg, France.ORCID 0009-0009-9272-7154
Ralph BockDepartment of Organelle Biology, Biotechnology and Molecular Ecophysiology, Max Planck Institute of Molecular Plant Physiology, D-14476 Potsdam-Golm, Germany.ORCID 0000-0001-7502-6940
Frédérique Weber-LotfiCNRS, Institut de Biologie Moléculaire des Plantes, University of Strasbourg, Strasbourg, France.ORCID 0000-0002-9482-550X
José M GualbertoCNRS, Institut de Biologie Moléculaire des Plantes, University of Strasbourg, Strasbourg, France.ORCID 0000-0002-7296-2618

Funding

French National Research AgencyLABEX ANR-11-LABX-0057_MITOCROSS
6 · The paper itself

Abstract

Maintenance of the plant organelle genomes involves factors mostly inherited from their symbiotic ancestors. In bacteria, DNA polymerase I (Pol I) performs multiple replication and repair functions through its 5'-3'-exonuclease/flap-endonuclease domain. Plant organelles possess 2 DNA polymerases that are evolutionarily derived from Pol I but lack this key domain. ORGANELLAR EXONUCLEASES 1 and 2 (OEX1 and OEX2) compensate for this missing function and are targeted to mitochondria and chloroplasts, respectively, in Arabidopsis (Arabidopsis thaliana). Loss of OEX1 causes developmental and fertility defects that increase with increasing differential segregation of mitochondrial DNA (mtDNA) subgenomes generated by recombination. OEX1 activity is modulated by alternative splicing, which generates 2 isoforms that variably affect mtDNA stability and repair. OEX1 has 5'-3'-exonuclease and flap endonuclease activities, with a high affinity for RNA-DNA hybrids. It rapidly degrades RNA in Okazaki-like structures and R-loops. Consistent with a role in suppressing R-loops, oex1 mutant plants accumulate RNA-DNA hybrids in highly transcribed mtDNA regions. Taken together, our results identify OEX1 as an important factor that compensates for the missing activity of plant organellar polymerases, playing multiple important roles in the processing of replication and recombination intermediates, such as replication primers and R-loops, whose accumulation can lead to genome instability.

Indexed as

ArabidopsisArabidopsis ProteinsExonucleasesFlap EndonucleasesGenome, MitochondrialGenomic InstabilityR-Loop StructuresDNA, MitochondrialDNA ReplicationMitochondriaArabidopsis ProteinsDNA, MitochondrialExonucleasesFlap Endonucleases

Identifiers

PMID40324391
PMCPMC12124402

What Socratic holds

Textmetadata
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 Socratic graph.