Evidence map›Paper›PMID 9128253›Full record

ArticleThe Journal of cell biology1997

A role for mitogen-activated protein kinase in the spindle assembly checkpoint in XTC cells.

X M Wang, Y Zhai, J E Ferrell

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 110 citations in OpenAlex.

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  13. The spindle checkpoint: a quality control mechanism which ensures accurate chromosome segregation.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2004
    Review
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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

3 authors at 2 institutions in 1 country.

X M WangDepartment of Molecular Pharmacology, Stanford University School of Medicine, California 94305-5332, USA.
Y Zhai
J E Ferrell
Stanford University · USUniversity of California, San Francisco · US

Funding

Leveraging innovative technologies in basic and clinical cancer researchT32CA009302 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI, Aaron M Newman · 1985 to 2026
$19.1M
THE ROLE OF MAP KINASE IN THE CELL CYCLER01GM046383 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI FERRELL, JAMES E. · 1991 to 2018
$7.3M
NCI NIH HHS CA09302NCI NIH HHS T32 CA009302NIGMS NIH HHS GM46383NIGMS NIH HHS R01 GM046383
6 · The paper itself

Abstract

The spindle assembly checkpoint prevents cells whose spindles are defective or chromosomes are misaligned from initiating anaphase and leaving mitosis. Studies of Xenopus egg extracts have implicated the Erk2 mitogen-activated protein kinase (MAP kinase) in this checkpoint. Other studies have suggested that MAP kinases might be important for normal mitotic progression. Here we have investigated whether MAP kinase function is required for mitotic progression or the spindle assembly checkpoint in vivo in Xenopus tadpole cells (XTC). We determined that Erk1 and/or Erk2 are present in the mitotic spindle during prometaphase and metaphase, consistent with the idea that MAP kinase might regulate or monitor the status of the spindle. Next, we microinjected purified recombinant XCL100, a Xenopus MAP kinase phosphatase, into XTC cells in various stages of mitosis to interfere with MAP kinase activation. We found that mitotic progression was unaffected by the phosphatase. However, XCL100 rendered the cells unable to remain arrested in mitosis after treatment with nocodazole. Cells injected with phosphatase at prometaphase or metaphase exited mitosis in the presence of nocodazole-the chromosomes decondensed and the nuclear envelope re-formed-whereas cells injected with buffer or a catalytically inactive XCL100 mutant protein remained arrested in mitosis. Coinjection of constitutively active MAP kinase kinase-1, which opposes XCL100's effects on MAP kinase, antagonized the effects of XCL100. Since the only known targets of MAP kinase kinase-1 are Erk1 and Erk2, these findings argue that MAP kinase function is required for the spindle assembly checkpoint in XTC cells.

Indexed as

Mitogen-Activated Protein Kinase KinasesXenopus ProteinsAnimalsCalcium-Calmodulin-Dependent Protein KinasesCell LineEnzyme ActivationImmediate-Early ProteinsMAP Kinase Kinase 1MetaphaseMicroinjectionsMicrotubulesMitogen-Activated Protein Kinase PhosphatasesMitosisNocodazoleProtein Serine-Threonine KinasesProtein-Tyrosine KinasesCalcium-Calmodulin-Dependent Protein KinasesDUSP1 protein, XenopusImmediate-Early ProteinsMAP Kinase Kinase 1Mitogen-Activated Protein Kinase KinasesMitogen-Activated Protein Kinase PhosphatasesNocodazoleProtein Serine-Threonine KinasesProtein-Tyrosine KinasesProtein Tyrosine PhosphatasesRecombinant Fusion ProteinsXenopus Proteins

Identifiers

PMID9128253
PMCPMC2139774
OpenAlexW2104764445

What Socratic 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 Socratic graph.