Evidence map›Paper›PMID 28314740›Full record

ArticleThe Journal of cell biology2017

Dual recognition of chromatin and microtubules by INCENP is important for mitotic progression.

Michael S Wheelock, David J Wynne, Boo Shan Tseng, Hironori Funabiki

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2017. 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
2.8field-weighted citation impact, top 10% 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, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

4 authors at 3 institutions in 1 country.

Michael S WheelockLaboratory of Chromosome and Cell Biology, The Rockefeller University, New York, NY 10065.
David J WynneLaboratory of Chromosome and Cell Biology, The Rockefeller University, New York, NY 10065.
Boo Shan TsengLaboratory of Chromosome and Cell Biology, The Rockefeller University, New York, NY 10065.ORCID 0000-0001-7563-0232
Hironori FunabikiLaboratory of Chromosome and Cell Biology, The Rockefeller University, New York, NY 10065 funabih@rockefeller.edu.ORCID 0000-0003-4831-4087
Rockefeller University · USCollege of New Jersey · USUniversity of Nevada, Las Vegas · US

Funding

Genetics and Cell BiologyT32GM066699 · NIGMS · ROCKEFELLER UNIVERSITY · PI STRICKLAND, SIDNEY · 2004 to 2021
$7.6M
Roles of Chromosomal Factors in Chromosome SegregationR01GM075249 · NIGMS · ROCKEFELLER UNIVERSITY · PI FUNABIKI, HIRONORI · 2005 to 2018
$4.5M
Acquisition of a DeltaVision OMX SR 3D SIM system for super-resolution imagingS10RR031855 · NCRR · ROCKEFELLER UNIVERSITY · PI NORTH, ALISON JANE · 2011 to 2011
$600k
Determining how the spindle assembly checkpoint monitors chromosome biorientationF32GM103147 · NIGMS · ROCKEFELLER UNIVERSITY · PI WYNNE, DAVID J · 2012 to 2013
$106k
NCRR NIH HHS S10 RR031855NIGMS NIH HHS F32 GM103147NIGMS NIH HHS R01 GM075249NIGMS NIH HHS T32 GM066699
6 · The paper itself

Abstract

The chromosomal passenger complex (CPC), composed of inner centromere protein (INCENP), Survivin, Borealin, and the kinase Aurora B, contributes to the activation of the mitotic checkpoint. The regulation of CPC function remains unclear. Here, we reveal that in addition to Survivin and Borealin, the single α-helix (SAH) domain of INCENP supports CPC localization to chromatin and the mitotic checkpoint. The INCENP SAH domain also mediates INCENP's microtubule binding, which is negatively regulated by Cyclin-dependent kinase-mediated phosphorylation of segments flanking the SAH domain. The microtubule-binding capacity of the SAH domain is important for mitotic arrest in conditions of suppressed microtubule dynamics, and the duration of mitotic arrest dictates the probability, but not the timing, of cell death. Although independent targeting of INCENP to microtubules or the kinetochore/centromere promotes the mitotic checkpoint, it is insufficient for a robust mitotic arrest. Altogether, our results demonstrate that dual recognition of chromatin and microtubules by CPC is important for checkpoint maintenance and determination of cell fate in mitosis.

Indexed as

Aurora Kinase BCell Line, TumorCentromereChromatinChromosomal Proteins, Non-HistoneCyclin-Dependent KinasesHeLa CellsHumansKinetochoresMicrotubule-Associated ProteinsMicrotubulesMitosisPhosphorylationProtein BindingProtein Serine-Threonine KinasesAurora Kinase BChromatinChromosomal Proteins, Non-HistoneCyclin-Dependent KinasesMicrotubule-Associated ProteinsProtein Serine-Threonine Kinases

Identifiers

PMID28314740
PMCPMC5379950
OpenAlexW2596045160

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.