Evidence map›Paper›PMID 14718559›Full record

ArticleMolecular biology of the cell2004

The transcriptome of prematurely aging yeast cells is similar to that of telomerase-deficient cells.

Isabelle Lesur, Judith L Campbell

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

54 citing papers in PubMed, 124 citations in OpenAlex.

  1. Article
  2. Transcriptional drift in aging cells: A global decontroller.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Review
  4. Transcriptional drift in aging cells: A global de-controller.bioRxiv : the preprint server for biology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Replicative Aging in Pathogenic Fungi.Journal of fungi (Basel, Switzerland) · 2020
    Review
  13. Review
  14. Review
  15. Epigenetic changes during aging and their reprogramming potential.Critical reviews in biochemistry and molecular biology · 2019
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Emerging Omics Approaches in Aging Research.Antioxidants & redox signaling · 2018
    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

2 authors at 1 institution in 2 countries.

Isabelle LesurBraun Laboratories 147-75, California Institute of Technology, Pasadena, California 91125, USA.
Judith L Campbell
California Institute of Technology · US

Funding

ENZYMATIC MECHANISMS OF DNA REPLICATIONR01GM025508 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CAMPBELL, JUDITH L · 1985 to 2006
$2.5M
NIGMS NIH HHS GM-25508NIGMS NIH HHS R01 GM025508
6 · The paper itself

Abstract

To help define the pathologies associated with yeast cells as they age, we analyzed the transcriptome of young and old cells isolated by elutriation, which allows isolation of biochemical quantities of old cells much further advanced in their life span than old cells prepared by the biotin-streptavidin method. Both 18-generation-old wild-type yeast and 8-generation-old cells from a prematurely aging mutant (dna2-1), with a defect in DNA replication, were evaluated. Genes involved in gluconeogenesis, the glyoxylate cycle, lipid metabolism, and glycogen production are induced in old cells, signifying a shift toward energy storage. We observed a much more extensive generalized stress response known as the environmental stress response (ESR), than observed previously in biotin-streptavidin-isolated cells, perhaps because the elutriated cells were further advanced in their life span. In addition, there was induction of DNA repair genes that fall in the so-called DNA damage "signature" set. In the dna2-1 mutant, energy production genes were also induced. The response in the dna2-1 strain is similar to the telomerase delete response, genes whose expression changes during cellular senescence in telomerase-deficient cells. We propose that these results suggest, albeit indirectly, that old cells are responding to genome instability.

Indexed as

Cell CycleCellular SenescenceDNA ReplicationGene Expression ProfilingGene Expression Regulation, FungalGenes, FungalMutationSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTelomeraseSaccharomyces cerevisiae ProteinsTelomerase

Identifiers

PMID14718559
PMCPMC363132
OpenAlexW2106244962

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.