Evidence map›Paper›PMID 30301808›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Human mitochondrial degradosome prevents harmful mitochondrial R loops and mitochondrial genome instability.

Sonia Silva, Lola P Camino, Andrés Aguilera

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

65 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
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  3. Biallelic variants inResearch square · 2026
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  11. Mitochondrial RNA in Inflammation.International journal of biological sciences · 2025
    Review
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  13. Review
  14. [SUV3 knockdown inhibits proliferation, migration, and invasion of hepatocellular carcinoma cells and induces PD-L1 expression].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
    Article
  15. Article
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  19. Type I IFN in Glomerular Disease: Scarring beyond the STING.International journal of molecular sciences · 2024
    Review
  20. Mechanisms and regulation of human mitochondrial transcription.Nature reviews. Molecular cell biology · 2024
    Review

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

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

3 authors at 1 institution in 1 country.

Sonia SilvaCentro Andaluz de Biología Molecular y Medicina Regenerativa, Universidad de Sevilla-Consejo Superior de Investigaciones Científicas-Universidad Pablo de Olavide, 41092 Seville, Spain.
Lola P CaminoCentro Andaluz de Biología Molecular y Medicina Regenerativa, Universidad de Sevilla-Consejo Superior de Investigaciones Científicas-Universidad Pablo de Olavide, 41092 Seville, Spain.
Andrés AguileraCentro Andaluz de Biología Molecular y Medicina Regenerativa, Universidad de Sevilla-Consejo Superior de Investigaciones Científicas-Universidad Pablo de Olavide, 41092 Seville, Spain aguilo@us.es.ORCID 0000-0003-4782-1714
Consejo Superior de Investigaciones Científicas · ES

Funding

European Research Council 669898
6 · The paper itself

Abstract

R loops are nucleic acid structures comprising an DNA-RNA hybrid and a displaced single-stranded DNA. These structures may occur transiently during transcription, playing essential biological functions. However, persistent R loops may become pathological as they are important drivers of genome instability and have been associated with human diseases. The mitochondrial degradosome is a functionally conserved complex from bacteria to human mitochondria. It is composed of the ATP-dependent RNA and DNA helicase SUV3 and the PNPase ribonuclease, playing a central role in mitochondrial RNA surveillance and degradation. Here we describe a new role for the mitochondrial degradosome in preventing the accumulation of pathological R loops in the mitochondrial DNA, in addition to preventing dsRNA accumulation. Our data indicate that, similar to the molecular mechanisms acting in the nucleus, RNA surveillance mechanisms in the mitochondria are crucial to maintain its genome integrity by counteracting pathological R-loop accumulation.

Indexed as

Cell Line, TumorDEAD-box RNA HelicasesDNA, MitochondrialDNA, Single-StrandedEndoribonucleasesExosome Multienzyme Ribonuclease ComplexGenome, MitochondrialGenomic InstabilityHeLa CellsHumansMitochondriaMultienzyme ComplexesPolyribonucleotide NucleotidyltransferaseRibonucleasesRNA, Double-StrandedRNA HelicasesDEAD-box RNA HelicasesdegradosomeDNA, MitochondrialDNA, Single-StrandedEndoribonucleasesExosome Multienzyme Ribonuclease ComplexMultienzyme ComplexesPolyribonucleotide NucleotidyltransferaseRibonucleasesRNA, Double-StrandedRNA Helicasesgenome instabilitymitochondrial degradosomeR loopsRNA metabolismtranscription–replication conflicts

Identifiers

PMID30301808
PMCPMC6205488
OpenAlexW2896633263

What OpenQuestion 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 OpenQuestion graph.