Evidence map›Paper›PMID 19920813›Full record

ArticleMolecular systems biology2009

Analysis of the mitotic exit control system using locked levels of stable mitotic cyclin.

Benjamin J Drapkin, Ying Lu, Andrea L Procko, Benjamin L Timney, Frederick R Cross

Open access · goldAbstract read
In one paragraph

Article in Molecular systems biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Hog1 activation delays mitotic exit via phosphorylation of Net1.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The Chlamydomonas cell cycle.The Plant journal : for cell and molecular biology · 2015
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. A quantitative model for cyclin-dependent kinase control of the cell cycle: revisited.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2011
    Review
  16. Article
  17. Article
  18. Article
  19. Frequency control of cell cycle oscillators.Current opinion in genetics & development · 2010
    Review
  20. 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

5 authors at 1 institution in 1 country.

Benjamin J DrapkinLaboratory of Yeast Molecular Genetics, The Rockefeller University, New York, NY 10021, USA.
Ying Lu
Andrea L Procko
Benjamin L Timney
Frederick R Cross
Rockefeller University · US

Funding

Stochastic Models of Cell Cycle Regulation in EukaryotesR01GM078989 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI PECCOUD, JEAN M, TYSON, JOHN J. · 2006 to 2018
$5.3M
Experimental and Computational Studies of Exit from Mitosis in Budding YeastR01GM079207 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI TYSON, JOHN J. · 2007 to 2010
$1.5M
NIGMS NIH HHS R01 GM078989NIGMS NIH HHS R01 GM079207
6 · The paper itself

Abstract

Cyclin-dependent kinase (Cdk) both promotes mitotic entry (spindle assembly and anaphase) and inhibits mitotic exit (spindle disassembly and cytokinesis), leading to an elegant quantitative hypothesis that a single cyclin oscillation can function as a ratchet to order these events. This ratchet is at the core of a published ODE model for the yeast cell cycle. However, the ratchet model requires appropriate cyclin dose-response thresholds. Here, we test the inhibition of mitotic exit in budding yeast using graded levels of stable mitotic cyclin (Clb2). In opposition to the ratchet model, stable levels of Clb2 introduced dose-dependent delays, rather than hard thresholds, that varied by mitotic exit event. The ensuing cell cycle was highly abnormal, suggesting a novel reason for cyclin degradation. Cdc14 phosphatase antagonizes Clb2-Cdk, and Cdc14 is released from inhibitory nucleolar sequestration independently of stable Clb2. Thus, Cdc14/Clb2 balance may be the appropriate variable for mitotic regulation. Although our results are inconsistent with the aforementioned ODE model, revision of the model to allow Cdc14/Clb2 balance to control mitotic exit corrects these discrepancies, providing theoretical support for our conclusions.

Indexed as

MitosisActive Transport, Cell NucleusAnaphaseBiosensing TechniquesCell NucleolusCyclin BG1 PhaseHistonesMating FactorModels, GeneticPeptidesPhosphoprotein PhosphatasesProtein KinasesProtein Processing, Post-TranslationalSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCLB2 protein, S cerevisiaeCyclin BHistonesMating FactorPeptidesPhosphoprotein PhosphatasesProtein KinasesSaccharomyces cerevisiae Proteins

Identifiers

PMID19920813
PMCPMC2795472
OpenAlexW2088091515

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.