Evidence map›Paper›PMID 20392738›Full record

ArticleJournal of cell science2010

APC16 is a conserved subunit of the anaphase-promoting complex/cyclosome.

Geert J P L Kops, Monique van der Voet, Moniek van der Voet, Michael S Manak, Maria H J van Osch, Said M Naini, Andrea Brear, Ian X McLeod, Dirk M Hentschel, John R Yates and 2 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. APC/CG3 (Bethesda, Md.) · 2017
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Structural insights into anaphase-promoting complex function and mechanism.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2011
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 2 countries.

Geert J P L KopsDepartment of Physiological Chemistry and Cancer Genomics Centre, UMC Utrecht, Utrecht, The Netherlands. g.j.p.l.kops@umcutrecht.nl
Monique van der Voet
Moniek van der Voet
Michael S Manak
Maria H J van Osch
Said M Naini
Andrea Brear
Ian X McLeod
Dirk M Hentschel
John R Yates
Sander van den Heuvel
Jagesh V Shah
Center for Systems Biology · USHarvard University · USScripps Research Institute · USUtrecht University · NLBrigham and Women's Hospital · USCancer Genomics Centre · NLUniversity Medical Center Utrecht · NL

Funding

ZDS2P REGULATES SWE1P-DEPENDENT POLARIZED CELL GROWTH IN S CEREVISIAEP41RR011823 · NCRR · UNIVERSITY OF WASHINGTON · PI DAVIS, TRACY · 1996 to 2011
$24.7M
Quantitative Measurements and Modeling of the Mitotic CheckpointR01GM077238 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI SHAH, JAGESH V · 2007 to 2011
$2.0M
NCRR NIH HHS P41 RR011823NCRR NIH HHS P41 RR11823NIGMS NIH HHS R01 GM077238NIGMS NIH HHS R01-GM077238
6 · The paper itself

Abstract

Error-free chromosome segregation depends on timely activation of the multi-subunit E3 ubiquitin ligase APC/C. Activation of the APC/C initiates chromosome segregation and mitotic exit by targeting critical cell-cycle regulators for destruction. The APC/C is the principle target of the mitotic checkpoint, which prevents segregation while chromosomes are unattached to spindle microtubules. We now report the identification and characterization of APC16, a conserved subunit of the APC/C. APC16 was found in association with tandem-affinity-purified mitotic checkpoint complex protein complexes. APC16 is a bona fide subunit of human APC/C: it is present in APC/C complexes throughout the cell cycle, the phenotype of APC16-depleted cells copies depletion of other APC/C subunits, and APC16 is important for APC/C activity towards mitotic substrates. APC16 sequence homologues can be identified in metazoans, but not fungi, by four conserved primary sequence stretches. We provide evidence that the C. elegans gene K10D2.4 and the D. rerio gene zgc:110659 are functional equivalents of human APC16. Our findings show that APC/C is composed of previously undescribed subunits, and raise the question of why metazoan APC/C is molecularly different from unicellular APC/C.

Indexed as

MitosisAnaphase-Promoting Complex-CyclosomeAnimalsCaenorhabditis elegansCalcium-Binding ProteinsCell Cycle ProteinsChromosome SegregationConserved SequenceHeLa CellsHumansMad2 ProteinsProtein BindingProtein Serine-Threonine KinasesProtein SubunitsRepressor ProteinsRNA, Small InterferingAnaphase-Promoting Complex-CyclosomeBub1 spindle checkpoint proteinCalcium-Binding ProteinsCell Cycle ProteinsMAD2L1 protein, humanMad2 ProteinsProtein Serine-Threonine KinasesProtein SubunitsRepressor ProteinsRNA, Small InterferingUbiquitin-Protein Ligase ComplexesUbiquitin-Protein Ligases

Identifiers

PMID20392738
PMCPMC2864710
OpenAlexW2144811445

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.