Evidence map›Paper›PMID 28573336›Full record

ArticleCurrent genetics2018

The influence of mitochondrial dynamics on mitochondrial genome stability.

Christopher T Prevost, Nicole Peris, Christina Seger, Deanna R Pedeville, Kathryn Wershing, Elaine A Sia, Rey A L Sia

Abstract read
PubMed Publisher
In one paragraph

Article in Current genetics, 2018. 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
1.2field-weighted citation impact, top 21% 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, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Aging: All roads lead to mitochondria.Seminars in cell & developmental biology · 2021
    Article
  5. Review
  6. Review
  7. Mitonuclear genomics and aging.Human genetics · 2020
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Organelle DNA contents and starch accumulation in potato tubers.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2019
    Article
  13. 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

7 authors at 2 institutions in 1 country.

Christopher T PrevostDepartment of Biology, University of Rochester, Rochester, NY, USA.
Nicole PerisDepartment of Biology, The College at Brockport, State University of New York, Brockport, NY, USA.
Christina SegerDepartment of Biology, The College at Brockport, State University of New York, Brockport, NY, USA.
Deanna R PedevilleDepartment of Biology, The College at Brockport, State University of New York, Brockport, NY, USA.
Kathryn WershingDepartment of Biology, The College at Brockport, State University of New York, Brockport, NY, USA.
Elaine A SiaDepartment of Biology, University of Rochester, Rochester, NY, USA. elaine.sia@rochester.edu.
Rey A L SiaDepartment of Biology, The College at Brockport, State University of New York, Brockport, NY, USA. rsia@brockport.edu.
SUNY Brockport · USUniversity of Rochester · US

Funding

National Science Foundation MCB0841857National Science Foundation MCB1243428University of Rochester OP212588
6 · The paper itself

Abstract

Mitochondria are dynamic organelles that fuse and divide. These changes alter the number and distribution of mitochondrial structures throughout the cell in response to developmental and metabolic cues. We have demonstrated that mitochondrial fission is essential to the maintenance of mitochondrial DNA (mtDNA) under changing metabolic conditions in wild-type Saccharomyces cerevisiae. While increased loss of mtDNA integrity has been demonstrated for dnm1-∆ fission mutants after growth in a non-fermentable carbon source, we demonstrate that growth of yeast in different carbon sources affects the frequency of mtDNA loss, even when the carbon sources are fermentable. In addition, we demonstrate that the impact of fission on mtDNA maintenance during growth in different carbon sources is neither mediated by retrograde signaling nor mitophagy. Instead, we demonstrate that mitochondrial distribution and mtDNA maintenance phenotypes conferred by loss of Dnm1p are suppressed by the loss of Sod2p, the mitochondrial matrix superoxide dismutase.

Indexed as

Genome, MitochondrialGenomic InstabilityMitochondrial DynamicsCarbonCell RespirationDNA Breaks, Double-StrandedDNA, MitochondrialDNA RepairGene DeletionGTP PhosphohydrolasesMitochondriaMitochondrial MembranesMitochondrial ProteinsMutationRaffinoseSaccharomyces cerevisiaeCarbonDNA, MitochondrialDNM1 protein, S cerevisiaeGTP PhosphohydrolasesMitochondrial ProteinsRaffinoseSaccharomyces cerevisiae ProteinsGenome instabilityMitochondriaMitochondrial DNA (mtDNA)Mitochondrial dynamicsMitochondrial genome

Identifiers

PMID28573336
OpenAlexW2620660505

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.