Evidence map›Paper›PMID 26247883›Full record

ArticlePLoS genetics2015

A Genome Scale Screen for Mutants with Delayed Exit from Mitosis: Ire1-Independent Induction of Autophagy Integrates ER Homeostasis into Mitotic Lifespan.

Ata Ghavidel, Kunal Baxi, Vladimir Ignatchenko, Martin Prusinkiewicz, Terra G Arnason, Thomas Kislinger, Carlos E Carvalho, Troy A A Harkness

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. "Janus-Faced" α-Synuclein: Role in Parkinson's Disease.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Review
  9. Protein quality control in the secretory pathway.The Journal of cell biology · 2019
    Review
  10. Review
  11. Article
  12. Article
  13. The role of autophagy in the regulation of yeast life span.Annals of the New York Academy of Sciences · 2018
    Review
  14. Some Metabolites Act as Second Messengers in Yeast Chronological Aging.International journal of molecular sciences · 2018
    Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. 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

8 authors at 2 institutions in 1 country.

Ata GhavidelDepartment of Anatomy & Cell Biology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Kunal BaxiDepartment of Biology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Vladimir IgnatchenkoDepartment of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
Martin PrusinkiewiczDepartment of Anatomy & Cell Biology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Terra G ArnasonDepartment of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Thomas KislingerDepartment of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
Carlos E CarvalhoDepartment of Biology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Troy A A HarknessDepartment of Anatomy & Cell Biology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
University of Saskatchewan · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proliferating eukaryotic cells undergo a finite number of cell divisions before irreversibly exiting mitosis. Yet pathways that normally limit the number of cell divisions remain poorly characterized. Here we describe a screen of a collection of 3762 single gene mutants in the yeast Saccharomyces cerevisiae, accounting for 2/3 of annotated yeast ORFs, to search for mutants that undergo an atypically high number of cell divisions. Many of the potential longevity genes map to cellular processes not previously implicated in mitotic senescence, suggesting that regulatory mechanisms governing mitotic exit may be broader than currently anticipated. We focused on an ER-Golgi gene cluster isolated in this screen to determine how these ubiquitous organelles integrate into mitotic longevity. We report that a chronic increase in ER protein load signals an expansion in the assembly of autophagosomes in an Ire1-independent manner, accelerates trafficking of high molecular weight protein aggregates from the cytoplasm to the vacuoles, and leads to a profound enhancement of daughter cell production. We demonstrate that this catabolic network is evolutionarily conserved, as it also extends reproductive lifespan in the nematode Caenorhabditis elegans. Our data provide evidence that catabolism of protein aggregates, a natural byproduct of high protein synthesis and turn over in dividing cells, is among the drivers of mitotic longevity in eukaryotes.

Indexed as

AutophagyMitosisAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsEndoplasmic ReticulumEndoplasmic Reticulum StressGenome, FungalGenome, HelminthHomeostasisMembrane GlycoproteinsProtein AggregatesProtein Serine-Threonine KinasesReproductionSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCaenorhabditis elegans ProteinsIRE1 protein, S cerevisiaeMembrane GlycoproteinsProtein AggregatesProtein Serine-Threonine KinasesRER1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsVesicular Transport Proteins

Identifiers

PMID26247883
PMCPMC4527830
OpenAlexW1541401001

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.