Evidence map›Paper›PMID 38337031›Full record

ArticleCommunications biology2024

Functional analysis of Cdc20 reveals a critical role of CRY box in mitotic checkpoint signaling.

Yuqing Zhang, Rose Young, Dimitriya H Garvanska, Chunlin Song, Yujing Zhai, Ying Wang, Hongfei Jiang, Jing Fang, Jakob Nilsson, Claudio Alfieri and 1 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. 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
2.6field-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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Generation of Cdc20 RNAi-Sensitive Cell Lines to Study Mitotic Exit.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  5. Review
  6. Review
  7. Novel regulation on the mitotic checkpoint revealed by knocking outFrontiers in cell and developmental biology · 2023
    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

11 authors at 3 institutions in 3 countries.

Yuqing ZhangCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Rose YoungChester Beatty Laboratories, Structural Biology Division, Institute of Cancer Research, London, UK.ORCID 0000-0001-9599-1414
Dimitriya H GarvanskaThe NNF Center for Protein Research, University of Copenhagen, Copenhagen, Denmark.
Chunlin SongCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Yujing ZhaiSchool of Public Health, Qingdao University, Qingdao, China.
Ying WangSchool of Public Health, Qingdao University, Qingdao, China.
Hongfei JiangCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.ORCID 0000-0001-5869-5253
Jing FangCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Jakob NilssonThe NNF Center for Protein Research, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-4100-1125
Claudio AlfieriChester Beatty Laboratories, Structural Biology Division, Institute of Cancer Research, London, UK. claudio.alfieri@icr.ac.uk.ORCID 0000-0003-3215-1607
Gang ZhangCancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China. zhanggang_sma@qdu.edu.cn.ORCID 0000-0001-7697-7203
Qingdao University · CNInstitute of Cancer Research · GBUniversity of Copenhagen · DK

Funding

Taishan Scholar Foundation of Shandong Province tsqn201812054
6 · The paper itself

Abstract

Accurate mitosis is coordinated by the spindle assembly checkpoint (SAC) through the mitotic checkpoint complex (MCC), which inhibits the anaphase-promoting complex or cyclosome (APC/C). As an essential regulator, Cdc20 promotes mitotic exit through activating APC/C and monitors kinetochore-microtubule attachment through activating SAC. Cdc20 requires multiple interactions with APC/C and MCC subunits to elicit these functions. Functionally assessing these interactions within cells requires efficient depletion of endogenous Cdc20, which is highly difficult to achieve by RNA interference (RNAi). Here we generated Cdc20 RNAi-sensitive cell lines which display a penetrant metaphase arrest by a single RNAi treatment. In this null background, we accurately measured the contribution of each known motif of Cdc20 on APC/C and SAC activation. The CRY box, a previously identified degron, was found critical for SAC by promoting MCC formation and its interaction with APC/C. These data reveal additional regulation within the SAC and establish a novel method to interrogate Cdc20.

Indexed as

Cdc20 ProteinsM Phase Cell Cycle CheckpointsSpindle ApparatusAnaphase-Promoting Complex-CyclosomeCell Cycle ProteinsHumansSignal TransductionAnaphase-Promoting Complex-CyclosomeCdc20 ProteinsCell Cycle Proteins

Identifiers

PMID38337031
PMCPMC10858191
OpenAlexW4391686730

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.