Evidence map›Paper›PMID 11134069›Full record

ArticleThe Journal of cell biology2000

Wee1-regulated apoptosis mediated by the crk adaptor protein in Xenopus egg extracts.

J J Smith, E K Evans, M Murakami, M B Moyer, M A Moseley, G Vande Woude, S Kornbluth

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  7. Loss of cryptochrome reduces cancer risk in p53 mutant mice.Proceedings of the National Academy of Sciences of the United States of America · 2009
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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

7 authors at 5 institutions in 1 country.

J J SmithDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.
E K Evans
M Murakami
M B Moyer
M A Moseley
G Vande Woude
S Kornbluth
Duke Medical Center · USResearch Triangle Park Foundation · USDuke University Hospital · USNational Cancer Institute · USVan Andel Institute · US

Funding

REGULATION OF APOPTOSISR01GM056518 · NIGMS · DUKE UNIVERSITY · PI KORNBLUTH, SALLY A · 1997 to 2006
$1.5M
NIGMS NIH HHS R01 GM056518NIGMS NIH HHS R01 GM56518
6 · The paper itself

Abstract

Many of the biochemical reactions of apoptotic cell death, including mitochondrial cytochrome c release and caspase activation, can be reconstituted in cell-free extracts derived from Xenopus eggs. In addition, because caspase activation does not occur until the egg extract has been incubated for several hours on the bench, upstream signaling processes occurring before full apoptosis are rendered accessible to biochemical manipulation. We reported previously that the adaptor protein Crk is required for apoptotic signaling in egg extracts (Evans, E.K., W. Lu, S.L. Strum, B.J. Mayer, and S. Kornbluth. 1997. EMBO (Eur. Mol. Biol. Organ.) J. 16:230-241). Moreover, we demonstrated that removal of Crk Src homology (SH)2 or SH3 interactors from the extracts prevented apoptosis. We now report the finding that the relevant Crk SH2-interacting protein, important for apoptotic signaling in the extract, is the well-known cell cycle regulator, Wee1. We have demonstrated a specific interaction between tyrosine-phosphorylated Wee1 and the Crk SH2 domain and have shown that recombinant Wee1 can restore apoptosis to an extract depleted of SH2 interactors. Moreover, exogenous Wee1 accelerated apoptosis in egg extracts, and this acceleration was largely dependent on the presence of endogenous Crk protein. As other Cdk inhibitors, such as roscovitine and Myt1, did not act like Wee1 to accelerate apoptosis, we propose that Wee1-Crk complexes signal in a novel apoptotic pathway, which may be unrelated to Wee1's role as a cell cycle regulator.

Indexed as

ApoptosisCell Cycle ProteinsNuclear ProteinsXenopus laevisXenopus ProteinsAmino Acid SequenceAnimalsCell ExtractsMolecular Sequence DataOvumPhosphorylationPhosphotyrosinePrecipitin TestsProtein BindingProtein Serine-Threonine KinasesProtein-Tyrosine KinasesCell Cycle ProteinsCell Extractscrk2 protein, XenopusMYT1 kinase, XenopusNuclear ProteinsPhosphotyrosineProtein Serine-Threonine KinasesProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-crkPurinesRoscovitineWEE1 protein, XenopusXenopus Proteins

Identifiers

PMID11134069
PMCPMC2150666
OpenAlexW2064919643

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.