Evidence map›Paper›PMID 26298836›Full record

ArticleDNA repair2015

Preferential retrotransposition in aging yeast mother cells is correlated with increased genome instability.

Melissa N Patterson, Alison E Scannapieco, Pak Ho Au, Savanna Dorsey, Catherine A Royer, Patrick H Maxwell

Abstract read
In one paragraph

Article in DNA repair, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
10.3field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. mRNA Isoforms and Variants in Health and Disease.International journal of molecular sciences · 2025
    Review
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  6. Elimination of virus-like particles reduces protein aggregation and extends replicative lifespan inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Article
  8. Article
  9. Article
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  15. The Retrotransposon storm and the dangers of a Collyer's genome.Current opinion in genetics & development · 2018
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Melissa N PattersonDepartment of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY, United States.
Alison E ScannapiecoDepartment of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY, United States.
Pak Ho AuDepartment of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY, United States.
Savanna DorseyDepartment of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY, United States.
Catherine A RoyerDepartment of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY, United States.
Patrick H MaxwellDepartment of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY, United States. Electronic address: maxwep2@rpi.edu.
Rensselaer Polytechnic Institute · US

Funding

Influence of Retrotransposition on DNA Damage and Repair in Aging CellsR00AG031911 · NIA · RENSSELAER POLYTECHNIC INSTITUTE · PI MAXWELL, PATRICK HENRY · 2011 to 2013
$718k
NIA NIH HHS R00 AG031911NIA NIH HHS R00AG031911
6 · The paper itself

Abstract

Retrotransposon expression or mobility is increased with age in multiple species and could promote genome instability or altered gene expression during aging. However, it is unclear whether activation of retrotransposons during aging is an indirect result of global changes in chromatin and gene regulation or a result of retrotransposon-specific mechanisms. Retromobility of a marked chromosomal Ty1 retrotransposon in Saccharomyces cerevisiae was elevated in mother cells relative to their daughter cells, as determined by magnetic cell sorting of mothers and daughters. Retromobility frequencies in aging mother cells were significantly higher than those predicted by cell age and the rate of mobility in young populations, beginning when mother cells were only several generations old. New Ty1 insertions in aging mothers were more strongly correlated with gross chromosome rearrangements than in young cells and were more often at non-preferred target sites. Mother cells were more likely to have high concentrations and bright foci of Ty1 Gag-GFP than their daughter cells. Levels of extrachromosomal Ty1 cDNA were also significantly higher in aged mother cell populations than their daughter cell populations. These observations are consistent with a retrotransposon-specific mechanism that causes retrotransposition to occur preferentially in yeast mother cells as they begin to age, as opposed to activation by phenotypic changes associated with very old age. These findings will likely be relevant for understanding retrotransposons and aging in many organisms, based on similarities in regulation and consequences of retrotransposition in diverse species.

Indexed as

Genome, FungalGenomic InstabilityCellular SenescenceChromosomes, FungalRetroelementsSaccharomyces cerevisiaeRetroelementsChromosome rearrangementsGagReplicative agingRetrotransposonSaccharomyces cerevisiaeTy1

Identifiers

PMID26298836
PMCPMC4592464
OpenAlexW1113174486

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.