Evidence map›Paper›PMID 11408585›Full record

ArticleMolecular biology of the cell2001

The polo-like kinase Plx1 is required for activation of the phosphatase Cdc25C and cyclin B-Cdc2 in Xenopus oocytes.

Y W Qian, E Erikson, F E Taieb, J L Maller

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 154 citations in OpenAlex.

  1. Article
  2. Article
  3. Biophysics reports · 2023
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. USP39 regulates the growth of SMMC-7721 cells via FoxM1.Experimental and therapeutic medicine · 2017
    Article
  10. Article
  11. Centrosomes as signalling centres.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Decoding ubiquitin for mitosis.Genes & cancer · 2012
    Article
  17. Pioneering the Xenopus oocyte and egg extract system.The Journal of biological chemistry · 2012
    Article
  18. Article
  19. Article
  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

4 authors at 1 institution in 1 country.

Y W QianHoward Hughes Medical Institute and Department of Pharmacology, University of Colorado School of Medicine, Denver, Colorado 80262, USA.
E Erikson
F E Taieb
J L Maller
Howard Hughes Medical Institute · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
S6 Phosphorylation &Tyrosine Protein KinasesR01DK028353 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MALLER, JAMES L · 1986 to 2004
$870k
CONTROL OF CELL DIVISION IN XENOPUS OOCYTESR01GM026743 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI MALLER, JAMES L · 1986 to 2003
$811k
NCI NIH HHS CA46934NCI NIH HHS P30 CA046934NIDDK NIH HHS DK28353-19NIDDK NIH HHS R01 DK028353NIGMS NIH HHS GM26743-21NIGMS NIH HHS R01 GM026743
6 · The paper itself

Abstract

In the Xenopus oocyte system mitogen treatment triggers the G(2)/M transition by transiently inhibiting the cAMP-dependent protein kinase (PKA); subsequently, other signal transduction pathways are activated, including the mitogen-activated protein kinase (MAPK) and polo-like kinase pathways. To study the interactions between these pathways, we have utilized a cell-free oocyte extract that carries out the signaling events of oocyte maturation after addition of the heat-stable inhibitor of PKA, PKI. PKI stimulated the synthesis of Mos and activation of both the MAPK pathway and the Plx1/Cdc25C/cyclin B-Cdc2 pathway. Activation of the MAPK pathway alone by glutathione S-transferase (GST)-Mos did not lead to activation of Plx1 or cyclin B-Cdc2. Inhibition of the MAPK pathway in the extract by the MEK1 inhibitor U0126 delayed, but did not prevent, activation of the Plx1 pathway, and inhibition of Mos synthesis by cycloheximide had a similar effect, suggesting that MAPK activation is the only relevant function of Mos. Immunodepletion of Plx1 completely inhibited activation of Cdc25C and cyclin B-Cdc2 by PKI, indicating that Plx1 is necessary for Cdc25C activation. In extracts containing fully activated Plx1 and Cdc25C, inhibition of cyclin B-Cdc2 by p21(Cip1) had no significant effect on either the phosphorylation of Cdc25C or the activity of Plx1. These results demonstrate that maintenance of Plx1 and Cdc25C activity during mitosis does not require cyclin B-Cdc2 activity.

Indexed as

Xenopus ProteinsAnimalscdc25 PhosphatasesCDC2 Protein KinaseCell Cycle ProteinsCyclic AMPCyclin BEnzyme ActivationG2 PhaseImmunoblottingOocytesPolo-Like Kinase 1Precipitin TestsProphaseProtein Serine-Threonine KinasesRNA, Messengercdc25 PhosphatasesCDC2 Protein KinaseCell Cycle ProteinsCyclic AMPCyclin BPlk1 protein, XenopusPolo-Like Kinase 1Protein Serine-Threonine KinasesRNA, MessengerXenopus Proteins

Identifiers

PMID11408585
PMCPMC37341
OpenAlexW2096750214

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.