Evidence map›Paper›PMID 17349956›Full record

ArticleMolecular cell2007

Evolution of Ime2 phosphorylation sites on Cdk1 substrates provides a mechanism to limit the effects of the phosphatase Cdc14 in meiosis.

Liam J Holt, Jessica E Hutti, Lewis C Cantley, David O Morgan

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

51 citing papers in PubMed, 75 citations in OpenAlex.

  1. Decoding Cdk1 control: from mitotic thresholds to meiotic specificity.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
    Review
  2. Article
  3. Article
  4. Meiotic Cytokinesis inJournal of fungi (Basel, Switzerland) · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Kar4, the Yeast Homolog of METTL14, is Required for mRNA mbioRxiv : the preprint server for biology · 2023
    Article
  9. Kar4 is Required for the Normal Pattern of Meiotic Gene Expression.bioRxiv : the preprint server for biology · 2023
    Article
  10. Article
  11. Phospho-Regulation of Meiotic Prophase.Frontiers in cell and developmental biology · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Meiosis: an overview of key differences from mitosis.Cold Spring Harbor perspectives in biology · 2015
    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

4 authors at 2 institutions in 1 country.

Liam J HoltDepartment of Physiology, University of California-San Francisco, San Francisco, CA 94158, USA.
Jessica E Hutti
Lewis C Cantley
David O Morgan
Harvard University · USUniversity of California, San Francisco · US

Funding

PROTEIN KINASE SIGNALING PATHWAYSR01GM056203 · NIGMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CANTLEY, LEWIS C. · 1997 to 2012
$4.5M
Cell Cycle Control by Cyclin-Dependent KinasesR01GM069901 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MORGAN, DAVID OWEN · 2004 to 2015
$3.6M
NIGMS NIH HHS GM 50684NIGMS NIH HHS GM 56203NIGMS NIH HHS R01 GM056203NIGMS NIH HHS R01 GM069901
6 · The paper itself

Abstract

Progression through meiosis in yeast is governed by the cyclin-dependent kinase Cdk1, in concert with a related kinase called Ime2. It remains unclear how these kinases collaborate to meet the unique demands of meiotic progression. We demonstrate that Ime2 and Cdk1 phosphorylate an overlapping substrate set and that the two kinases overlap functionally as inhibitors of the ubiquitin ligase APC(Cdh1) and replication origin licensing. Surprisingly, Ime2 phosphorylates Cdk1 substrates at distinct phosphorylation sites that are highly resistant to dephosphorylation by the phosphatase Cdc14. We propose that Ime2-dependent phosphorylation of a subset of cell-cycle proteins limits the effects of Cdc14 in meiosis.

Indexed as

Evolution, MolecularMeiosisActive Transport, Cell NucleusAmino Acid SequenceCDC2 Protein KinaseCell Cycle ProteinsCell NucleusChromosomal Proteins, Non-HistoneConsensus SequenceDNA ReplicationFungal ProteinsIntracellular Signaling Peptides and ProteinsModels, BiologicalMolecular Sequence DataPhosphatesPhosphoprotein PhosphatasesCDC14 protein, S cerevisiaeCDC2 Protein KinaseCell Cycle ProteinsChromosomal Proteins, Non-HistoneFungal ProteinsIME2 protein, S cerevisiaeIntracellular Signaling Peptides and ProteinsMCM2 protein, S cerevisiaePhosphatesPhosphoprotein PhosphatasesProtein KinasesProtein Serine-Threonine KinasesProtein Tyrosine PhosphatasesSaccharomyces cerevisiae Proteins

Identifiers

PMID17349956
PMCPMC1939968
OpenAlexW2094309012

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.