Evidence map›Paper›PMID 28189585›Full record

ArticleCellular signalling2017

Transcriptional and post-transcriptional regulation of Cdc20 during the spindle assembly checkpoint in S. cerevisiae.

Ruiwen Wang, Janet L Burton, Mark J Solomon

Abstract read
In one paragraph

Article in Cellular signalling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. The Protein Response of Salt-TolerantJournal of fungi (Basel, Switzerland) · 2024
    Article
  4. Article
  5. Article
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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 2 countries.

Ruiwen WangInstitute of Life Sciences, College of Biological Science and Engineering, Fuzhou University, Fuzhou, Fujian Province 350108, China. Electronic address: ruiwen.wang@fzu.edu.cn.
Janet L BurtonDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520-8114, USA.
Mark J SolomonDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520-8114, USA. Electronic address: Mark.Solomon@Yale.edu.
Yale University · USFuzhou University · CN

Funding

Biochemistry of Anaphase Promoting Complex-mediated UbiquitinationR01GM101044 · NIGMS · YALE UNIVERSITY · PI SOLOMON, MARK J · 2013 to 2016
$1.3M
NIGMS NIH HHS R01 GM101044
6 · The paper itself

Abstract

The anaphase-promoting complex (APC) is a ubiquitin ligase responsible for promoting the degradation of many cell cycle regulators. One of the activators and substrate-binding proteins for the APC is Cdc20. It has been shown previously that Cdc20 can promote its own degradation by the APC in normal cycling cells mainly through a cis-degradation mode (i.e. via an intramolecular mechanism). However, how Cdc20 is degraded during the spindle assembly checkpoint (SAC) is still not fully clear. In this study, we used a dual-Cdc20 system to investigate this issue and found that the cis-degradation mode is also the major pathway responsible for Cdc20 degradation during the SAC. In addition, we found that there is an inverse relationship between APC

Indexed as

Gene Expression Regulation, FungalTranscription, GeneticAmino Acid MotifsAnaphase-Promoting Complex-CyclosomeCdc20 ProteinsM Phase Cell Cycle CheckpointsPromoter Regions, GeneticProteolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSubstrate SpecificityAnaphase-Promoting Complex-CyclosomeCdc20 ProteinsCDC20 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsAnaphase-promoting complexCdc20Post-transcriptional regulationProtein degradationSpindle assembly checkpointUbiquitination

Identifiers

PMID28189585
PMCPMC5394925
OpenAlexW2587150965

What OpenQuestion holds

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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.