Evidence map›Paper›PMID 35238874›Full record

ArticleThe Journal of cell biology2022

Cdc14 spatiotemporally dephosphorylates Atg13 to activate autophagy during meiotic divisions.

Wenzhi Feng, Orlando Argüello-Miranda, Suhong Qian, Fei Wang

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Membrane and organelle rearrangement during ascospore formation in budding yeast.Microbiology and molecular biology reviews : MMBR · 2024
    Review
  5. Meiotic Cytokinesis inJournal of fungi (Basel, Switzerland) · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Wenzhi FengDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0002-5597-9530
Orlando Argüello-MirandaDepartment of Plant and Microbial Biology, North Carolina State University, Raleigh, NC.ORCID 0000-0002-0579-4650
Suhong QianDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0002-4424-6526
Fei WangDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0001-7899-244X
The University of Texas Southwestern Medical Center · USNorth Carolina State University · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
Mechanistic dissection of a novel meiotic exit regulation by autophagy - Equipment SupplementR01GM133899 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI WANG, FEI · 2020 to 2024
$1.9M
Spinning Disk Confocal for UT SouthwesternS10OD028630 · OD · UT SOUTHWESTERN MEDICAL CENTER · PI LUBY-PHELPS, KATHERINE J · 2020 to 2020
$600k
Systems biology of quiescence entryK99GM135487 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI ARGÜELLO-MIRANDA, ORLANDO · 2020 to 2021
$192k
NCI NIH HHS P30 CA142543NIGMS NIH HHS K99 GM135487NIGMS NIH HHS R01 GM133899NIH HHS R01GM133899NIH HHS S10 OD028630
6 · The paper itself

Abstract

Autophagy is a conserved eukaryotic lysosomal degradation pathway that responds to environmental and cellular cues. Autophagy is essential for the meiotic exit and sporulation in budding yeast, but the underlying molecular mechanisms remain unknown. Here, we show that autophagy is maintained during meiosis and stimulated in anaphase I and II. Cells with higher levels of autophagy complete meiosis faster, and genetically enhanced autophagy increases meiotic kinetics and sporulation efficiency. Strikingly, our data reveal that the conserved phosphatase Cdc14 regulates meiosis-specific autophagy. Cdc14 is activated in anaphase I and II, accompanying its subcellular relocation from the nucleolus to the cytoplasm, where it dephosphorylates Atg13 to stimulate Atg1 kinase activity and thus autophagy. Together, our findings reveal a meiosis-tailored mechanism that spatiotemporally controls meiotic autophagy activity to ensure meiosis progression, exit, and sporulation.

Indexed as

Adaptor Proteins, Signal TransducingAutophagyAutophagy-Related ProteinsCell Cycle ProteinsProtein Tyrosine PhosphatasesSaccharomyces cerevisiae ProteinsAnaphaseMeiosisAdaptor Proteins, Signal TransducingATG13 protein, S cerevisiaeAutophagy-Related ProteinsCDC14 protein, S cerevisiaeCell Cycle ProteinsProtein Tyrosine PhosphatasesSaccharomyces cerevisiae Proteins

Identifiers

PMID35238874
PMCPMC8919667
OpenAlexW4214824765

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.