Evidence map›Paper›PMID 24323947›Full record

ArticleAging2013

Transposable elements become active and mobile in the genomes of aging mammalian somatic tissues.

Marco De Cecco, Steven W Criscione, Abigail L Peterson, Nicola Neretti, John M Sedivy, Jill A Kreiling

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 224 papers.

0numbers the graph read from it
0cells of the map it votes in
224citing papers in PubMed
22.2field-weighted citation impact, top 1% 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

224 citing papers in PubMed, 381 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Characterization of Cellular Senescence in Primary Human Astrocytes.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Extrachromosomal Circular DNA and Transposable Elements in Type 2 Diabetes.International journal of molecular sciences · 2025
    Review
  16. A multi-omics analysis of human fibroblasts overexpressing anbioRxiv : the preprint server for biology · 2025
    Article
  17. Article
  18. Article
  19. Review
  20. Review

164 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

6 authors at 1 institution in 1 country.

Marco De CeccoDepartment of Molecular Biology, Cell Biology and Biochemistry, Center for Genomics and Proteomics, Brown University, Providence, RI 02903, USA.
Steven W Criscione
Abigail L Peterson
Nicola Neretti
John M Sedivy
Jill A Kreiling
Brown University · US

Funding

TRAINING IN MOLECULAR &CELL BIOLOGY &BIOCHEMISTRYT32GM007601 · NIGMS · BROWN UNIVERSITY · PI MOWRY, KIMBERLY L. · 1985 to 2019
$6.4M
Center for Cancer Signaling NetworksP30GM103410 · NIGMS · BROWN UNIVERSITY · PI ATWOOD, WALTER J · 2012 to 2015
$4.3M
Effectors of cellular senescence statesR37AG016694 · NIA · BROWN UNIVERSITY · PI SEDIVY, JOHN M · 2009 to 2018
$3.2M
The Wnt-chromatin axis in agingR01AG035328 · NIA · BROWN UNIVERSITY · PI SEDIVY, JOHN M · 2009 to 2011
$952k
Computational Biology of Transcriptional Networks in AgingK25AG028753 · NIA · BROWN UNIVERSITY · PI NERETTI, NICOLA · 2007 to 2011
$693k
Regulation of Age-Associated Heterochromatin FormationK01AG039410 · NIA · BROWN UNIVERSITY · PI KREILING, JILL · 2011 to 2015
$582k
NIA NIH HHS K01 AG039410NIA NIH HHS K25 AG028753NIA NIH HHS R01 AG035328NIA NIH HHS R37 AG016694NIA NIH HHS R37AG016694NIGMS NIH HHS P30 GM0103410NIGMS NIH HHS P30 GM103410NIGMS NIH HHS T32 GM007601
6 · The paper itself

Abstract

Transposable elements (TEs) were discovered by Barbara McClintock in maize and have since been found to be ubiquitous in all living organisms. Transposition is mutagenic and organisms have evolved mechanisms to repress the activity of their endogenous TEs. Transposition in somatic cells is very low, but recent evidence suggests that it may be derepressed in some cases, such as cancer development. We have found that during normal aging several families of retrotransposable elements (RTEs) start being transcribed in mouse tissues. In advanced age the expression culminates in active transposition. These processes are counteracted by calorie restriction (CR), an intervention that slows down aging. Retrotransposition is also activated in age-associated, naturally occurring cancers in the mouse. We suggest that somatic retrotransposition is a hitherto unappreciated aging process. Mobilization of RTEs is likely to be an important contributor to the progressive dysfunction of aging cells.

Indexed as

GenomeAgingAnimalsCaloric RestrictionDeoxyribonucleasesDNA Transposable ElementsGene Expression RegulationLiverMiceMicrosatellite RepeatsRNA, MessengerDeoxyribonucleasesDNA Transposable ElementsRNA, Messenger

Identifiers

PMID24323947
PMCPMC3883704
OpenAlexW2150453771

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.