Evidence map›Paper›PMID 26206521›Full record

ArticleScientific reports2015

Spatiotemporal dynamics of Aurora B-PLK1-MCAK signaling axis orchestrates kinetochore bi-orientation and faithful chromosome segregation.

Hengyi Shao, Yuejia Huang, Liangyu Zhang, Kai Yuan, Youjun Chu, Zhen Dou, Changjiang Jin, Minerva Garcia-Barrio, Xing Liu, Xuebiao Yao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

41 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Zombies Never Die: The Double Life Bub1 Lives in Mitosis.Frontiers in cell and developmental biology · 2022
    Review
  15. Review
  16. KIF2C promotes the proliferation of hepatocellular carcinoma cellsExperimental and therapeutic medicine · 2021
    Article
  17. Article
  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

10 authors at 3 institutions in 2 countries.

Hengyi ShaoAnhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science &Technology of China, Hefei 230027, China.
Yuejia Huang1] Anhui-MSM Joint Research Group for Cellular Dynamics, Hefei National Laboratory for Physical Sciences at Nanoscale, Hefei 230027, China [2] Department of Physiology, Morehouse School of Medicine, Atlanta, GA 30310, USA.
Liangyu Zhang1] Anhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science &Technology of China, Hefei 230027, China [2] Department of Physiology, Morehouse School of Medicine, Atlanta, GA 30310, USA.
Kai YuanAnhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science &Technology of China, Hefei 230027, China.
Youjun Chu1] Anhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science &Technology of China, Hefei 230027, China [2] Department of Physiology, Morehouse School of Medicine, Atlanta, GA 30310, USA.
Zhen Dou1] Anhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science &Technology of China, Hefei 230027, China [2] Anhui-MSM Joint Research Group for Cellular Dynamics, Hefei National Laboratory for Physical Sciences at Nanoscale, Hefei 230027, China.
Changjiang JinAnhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science &Technology of China, Hefei 230027, China.
Minerva Garcia-BarrioDepartment of Physiology, Morehouse School of Medicine, Atlanta, GA 30310, USA.
Xing Liu1] Anhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science &Technology of China, Hefei 230027, China [2] Anhui-MSM Joint Research Group for Cellular Dynamics, Hefei National Laboratory for Physical Sciences at Nanoscale, Hefei 230027, China [3] Department of Physiology, Morehouse School of Medicine, Atlanta, GA 30310, USA.
Xuebiao YaoAnhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science &Technology of China, Hefei 230027, China.
University of Science and Technology of China · CNHefei National Center for Physical Sciences at Nanoscale · CNMorehouse School of Medicine · US

Funding

The function of ezrin in stimulus-coupled acid secretionR01DK056292 · NIDDK · UNIVERSITY OF WISCONSIN MADISON · PI YAO, XUEBIAO · 1999 to 2012
$2.5M
Function of ACAP4 in CCL18-stimulated breast cancer metastasisR01CA164133 · NCI · MOREHOUSE SCHOOL OF MEDICINE · PI YAO, XUEBIAO · 2012 to 2016
$1.4M
NCI NIH HHS CA164133NCI NIH HHS R01 CA164133NIDDK NIH HHS DK56292NIDDK NIH HHS R01 DK056292
6 · The paper itself

Abstract

Chromosome segregation in mitosis is orchestrated by the dynamic interactions between the kinetochore and spindle microtubules. The microtubule depolymerase mitotic centromere-associated kinesin (MCAK) is a key regulator for an accurate kinetochore-microtubule attachment. However, the regulatory mechanism underlying precise MCAK depolymerase activity control during mitosis remains elusive. Here, we describe a novel pathway involving an Aurora B-PLK1 axis for regulation of MCAK activity in mitosis. Aurora B phosphorylates PLK1 on Thr210 to activate its kinase activity at the kinetochores during mitosis. Aurora B-orchestrated PLK1 kinase activity was examined in real-time mitosis using a fluorescence resonance energy transfer-based reporter and quantitative analysis of native PLK1 substrate phosphorylation. Active PLK1, in turn, phosphorylates MCAK at Ser715 which promotes its microtubule depolymerase activity essential for faithful chromosome segregation. Importantly, inhibition of PLK1 kinase activity or expression of a non-phosphorylatable MCAK mutant prevents correct kinetochore-microtubule attachment, resulting in abnormal anaphase with chromosome bridges. We reason that the Aurora B-PLK1 signaling at the kinetochore orchestrates MCAK activity, which is essential for timely correction of aberrant kinetochore attachment to ensure accurate chromosome segregation during mitosis.

Indexed as

Aurora Kinase BCell Cycle ProteinsChromosome SegregationChromosomes, HumanHeLa CellsHumansKinesinsKinetochoresMitosisPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsAURKB protein, humanAurora Kinase BCell Cycle ProteinsKIF2C protein, humanKinesinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteins

Identifiers

PMID26206521
PMCPMC4513279
OpenAlexW977115333

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.