Evidence map›Paper›PMID 26462070›Full record

ArticlePloS one2015

Human REV3 DNA Polymerase Zeta Localizes to Mitochondria and Protects the Mitochondrial Genome.

Bhupendra Singh, Xiurong Li, Kjerstin M Owens, Ayyasamy Vanniarajan, Ping Liang, Keshav K Singh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Mitochondrial DNA Instability in Mammalian Cells.Antioxidants & redox signaling · 2022
    Review
  7. Article
  8. Genes · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. The Mitochondrial Response to DNA Damage.Frontiers in cell and developmental biology · 2021
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Mitochondria-Modulating Porous Se@SiOInternational journal of nanomedicine · 2020
    Article
  19. Review
  20. Mitochondrial DNA: Epigenetics and environment.Environmental and molecular mutagenesis · 2019
    Review
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

6 authors at 4 institutions in 2 countries.

Bhupendra SinghDepartment of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Xiurong LiDepartment of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Kjerstin M OwensDepartment of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Ayyasamy VanniarajanDepartment of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, New York, United States of America.
Ping LiangDepartment of Biological Sciences, Brock University, St. Catharine's, Ontario, Canada.
Keshav K SinghDepartments of Genetics, Pathology, Environmental Health, Center for Free Radical Biology, Center for Aging and UAB Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, Alabama, United States of America; Birmingham Veterans Affairs Medical Center, Birmingham, Alabama, United States of America.
Roswell Park Comprehensive Cancer Center · USUniversity of Alabama at Birmingham · USBrock University · CACancer Genetics (United States) · US

Funding

BLRD VA I01 BX001716
6 · The paper itself

Abstract

To date, mitochondrial DNA polymerase γ (POLG) is the only polymerase known to be present in mammalian mitochondria. A dogma in the mitochondria field is that there is no other polymerase present in the mitochondria of mammalian cells. Here we demonstrate localization of REV3 DNA polymerase in the mammalian mitochondria. We demonstrate localization of REV3 in the mitochondria of mammalian tissue as well as cell lines. REV3 associates with POLG and mitochondrial DNA and protects the mitochondrial genome from DNA damage. Inactivation of Rev3 leads to reduced mitochondrial membrane potential, reduced OXPHOS activity, and increased glucose consumption. Conversely, inhibition of the OXPHOS increases expression of Rev3. Rev3 expression is increased in human primary breast tumors and breast cancer cell lines. Inactivation of Rev3 decreases cell migration and invasion, and localization of Rev3 in mitochondria increases survival and the invasive potential of cancer cells. Taken together, we demonstrate that REV3 functions in mammalian mitochondria and that mitochondrial REV3 is associated with the tumorigenic potential of cells.

Indexed as

Genome, MitochondrialAmino Acid SequenceAnimalsBreast NeoplasmsCarcinogenesisCell Line, TumorCytoprotectionDNA-Binding ProteinsDNA DamageDNA-Directed DNA PolymeraseDNA, MitochondrialDNA Polymerase gammaFemaleHEK293 CellsHeLa CellsHumansDNA-Binding ProteinsDNA-Directed DNA PolymeraseDNA, MitochondrialDNA Polymerase gammaREV3L protein, human

Identifiers

PMID26462070
PMCPMC4604079
OpenAlexW2338385528

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.