Evidence map›Paper›PMID 33540226›Full record

ArticleDNA repair2021

DNA polymerase β outperforms DNA polymerase γ in key mitochondrial base excision repair activities.

Beverly A Baptiste, Stephanie L Baringer, Tomasz Kulikowicz, Joshua A Sommers, Deborah L Croteau, Robert M Brosh, Vilhelm A Bohr

Open access · greenAbstract readComparative Study
In one paragraph

Article in DNA repair, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. Article
  7. Mitochondrial DNA damage as driver of cellular outcomes.American journal of physiology. Cell physiology · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Article
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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

7 authors at 1 institution in 1 country.

Beverly A BaptisteLaboratory of Molecular Gerontology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD, 21224, USA.
Stephanie L BaringerLaboratory of Molecular Gerontology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD, 21224, USA.
Tomasz KulikowiczLaboratory of Molecular Gerontology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD, 21224, USA.
Joshua A SommersLaboratory of Molecular Gerontology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD, 21224, USA.
Deborah L CroteauLaboratory of Molecular Gerontology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD, 21224, USA.
Robert M BroshLaboratory of Molecular Gerontology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD, 21224, USA.
Vilhelm A BohrLaboratory of Molecular Gerontology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD, 21224, USA. Electronic address: vbohr@nih.gov.
National Institute on Aging · US

Funding

Mitochondrial DNA Repair Processes In Oxidative Stress And AgingZIAAG000733 · NIA · NATIONAL INSTITUTE ON AGING · PI FERRUCCI, LUIGI · 2009 to 2022
$9.2M
Oxidative DNA Damage And Its ProcessingZIAAG000727 · NIA · NATIONAL INSTITUTE ON AGING · PI FERRUCCI, LUIGI · 2009 to 2022
$8.4M
Roles Of DNA Helicases In Pathways Required For Maintenance Of Genomic StabilityZIAAG000741 · NIA · NATIONAL INSTITUTE ON AGING · PI BROSH, ROBERT · 2009 to 2025
$7.6M
Model Genetic Systems to Study DNA RepairZIAAG000752 · NIA · NATIONAL INSTITUTE ON AGING · PI BROSH, ROBERT · 2009 to 2025
$4.8M
OXIDATIVE STRESS MITOCHONDRIAZ01AG000733 · NIA · NATIONAL INSTITUTE ON AGING · PI BOHR, VILHELM A · 1996 to 2008
$1.6M
Intramural NIH HHS Z01 AG000733
6 · The paper itself

Abstract

DNA polymerase beta (POLβ), well known for its role in nuclear DNA base excision repair (BER), has been shown to be present in the mitochondria of several different cell types. Here we present a side-by-side comparison of BER activities of POLβ and POLγ, the mitochondrial replicative polymerase, previously thought to be the only mitochondrial polymerase. We find that POLβ is significantly more proficient at single-nucleotide gap filling, both in substrates with ends that require polymerase processing, and those that do not. We also show that POLβ has a helicase-independent functional interaction with the mitochondrial helicase, TWINKLE. This interaction stimulates strand-displacement synthesis, but not single-nucleotide gap filling. Importantly, we find that purified mitochondrial extracts from cells lacking POLβ are severely deficient in processing BER intermediates, suggesting that mitochondrially localized DNA POLβ may be critical for cells with high energetic demands that produce greater levels of oxidative stress and therefore depend upon efficient BER for mitochondrial health.

Indexed as

DNA RepairAnimalsDNA DamageDNA, MitochondrialDNA Polymerase betaDNA Polymerase gammaMiceMitochondriaDNA, MitochondrialDNA Polymerase betaDNA Polymerase gammaBerMitochondriaPolbPolg

Identifiers

PMID33540226
PMCPMC7887074
OpenAlexW3122895185

What OpenQuestion holds

Textmetadata
LicenceTDM
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.