Evidence map›Paper›PMID 22021441›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Retrotransposition is associated with genome instability during chronological aging.

Patrick H Maxwell, William C Burhans, M Joan Curcio

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

85 citing papers in PubMed, 144 citations in OpenAlex.

  1. Article
  2. Regulatory roles of PIWI-interacting RNAs in cardiovascular disease.American journal of physiology. Heart and circulatory physiology · 2025
    Review
  3. Review
  4. Article
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  6. Article
  7. Article
  8. Review
  9. Transposon control as a checkpoint for tissue regeneration.Development (Cambridge, England) · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. The effect of environmental stress on ageing in a termite species with low social complexity.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  19. Why and how do termite kings and queens live so long?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  20. Article

25 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 3 institutions in 1 country.

Patrick H MaxwellLaboratory of Molecular Genetics, Wadsworth Center, and Department of Biomedical Sciences, School of Public Health, University at Albany, State University of New York, Albany, NY 12201-2002, USA. maxwep2@rpi.edu
William C Burhans
M Joan Curcio
Roswell Park Comprehensive Cancer Center · USUniversity at Albany, State University of New York · USWadsworth Center · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
REGULATION OF RETROTRANSPOSITION IN S. CEREVISIAER01GM052072 · NIGMS · WADSWORTH CENTER · PI CURCIO, M JOAN · 2000 to 2013
$3.3M
Influence of Retrotransposition on DNA Damage and Repair in Aging CellsR00AG031911 · NIA · RENSSELAER POLYTECHNIC INSTITUTE · PI MAXWELL, PATRICK HENRY · 2011 to 2013
$718k
Influence of Retrotransposition on DNA Damage and Repair in Aging CellsK99AG031911 · NIA · WADSWORTH CENTER · PI MAXWELL, PATRICK H · 2009 to 2009
$81k
REGULATION OF RETROTRANSPOSITION IN S CEREVISIAER29GM052072 · NIGMS · WADSWORTH CENTER · PI CURCIO, M JOAN · 1995 to 1999
–
NCI NIH HHS CA016056NCI NIH HHS P30 CA016056NIA NIH HHS K99 AG031911NIA NIH HHS K99AG031911NIA NIH HHS R00 AG031911NIGMS NIH HHS GM52072NIGMS NIH HHS R01 GM052072NIGMS NIH HHS R29 GM052072
6 · The paper itself

Abstract

Genetic damage through mutations and genome rearrangements has been hypothesized to contribute to aging. The specific mechanisms responsible for age-induced increases in mutation and chromosome rearrangement frequencies and a potential causative role for DNA damage in aging are under active investigation. Retrotransposons are mobile genetic elements that cause insertion mutations and contribute to genome rearrangements through nonallelic recombination events in humans and other organisms. We have investigated the role of endogenous Ty1 retrotransposons in aging-associated increases in genome instability using the Saccharomyces cerevisiae chronological aging model. We show that age-induced increases in loss of heterozygosity and chromosome loss events are consistently diminished by mutations or treatments that reduce Ty1 retrotransposition. Ty1 mobility is elevated in very old yeast populations, and new retromobility events are often associated with chromosome rearrangements. These results reveal a correlation between retrotransposition and genome instability during yeast aging. Retrotransposition may contribute to genetic damage during aging in diverse organisms and provides a useful tool for studying whether genetic damage is a causative factor for aging.

Indexed as

Cell SurvivalChromosomesDNA DamageGene DeletionGene RearrangementGenes, FungalGenomeGenome, FungalLoss of HeterozygosityMutationRetroelementsSaccharomyces cerevisiaeTime FactorsRetroelements

Identifiers

PMID22021441
PMCPMC3251071
OpenAlexW2093935371

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.