Evidence map›Paper›PMID 28751710›Full record

ArticleNature communications2017

Aurora-B kinase pathway controls the lateral to end-on conversion of kinetochore-microtubule attachments in human cells.

Roshan L Shrestha, Duccio Conti, Naoka Tamura, Dominique Braun, Revathy A Ramalingam, Konstanty Cieslinski, Jonas Ries, Viji M Draviam

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
–field-weighted citation impact
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

51 citing papers in PubMed.

  1. Review
  2. Article
  3. Countervailing effects of cyclin isoforms A and B during mitosis.bioRxiv : the preprint server for biology · 2026
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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

8 authors.

Roshan L ShresthaDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK.
Duccio ContiDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK.
Naoka TamuraDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK.
Dominique BraunDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK.
Revathy A RamalingamSchool of Biological and Chemical Sciences, Queen Mary University of London, London, E1 4NS, UK.
Konstanty CieslinskiEuropean Molecular Biology Laboratory, Cell Biology and Biophysics Unit, Meyerhofstrasse 1, Heidelberg, Germany.
Jonas RiesEuropean Molecular Biology Laboratory, Cell Biology and Biophysics Unit, Meyerhofstrasse 1, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-6640-9250
Viji M DraviamDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK. v.draviam@qmul.ac.uk.

Funding

Cancer Research UK 9787
6 · The paper itself

Abstract

Human chromosomes are captured along microtubule walls (lateral attachment) and then tethered to microtubule-ends (end-on attachment) through a multi-step end-on conversion process. Upstream regulators that orchestrate this remarkable change in the plane of kinetochore-microtubule attachment in human cells are not known. By tracking kinetochore movements and using kinetochore markers specific to attachment status, we reveal a spatially defined role for Aurora-B kinase in retarding the end-on conversion process. To understand how Aurora-B activity is counteracted, we compare the roles of two outer-kinetochore bound phosphatases and find that BubR1-associated PP2A, unlike KNL1-associated PP1, plays a significant role in end-on conversion. Finally, we uncover a novel role for Aurora-B regulated Astrin-SKAP complex in ensuring the correct plane of kinetochore-microtubule attachment. Thus, we identify Aurora-B as a key upstream regulator of end-on conversion in human cells and establish a late role for Astrin-SKAP complex in the end-on conversion process.Human chromosomes are captured along microtubule walls and then tethered to microtubule-ends through a multi-step end-on conversion process. Here the authors show that Aurora-B regulates end-on conversion in human cells and establish a late role for Astrin-SKAP complex in the end-on conversion process.

Indexed as

Signal TransductionAurora Kinase BCell Cycle ProteinsHeLa CellsHumansImmunoblottingKinetochoresMicroscopy, FluorescenceMicrotubule-Associated ProteinsMicrotubulesPhosphoric Monoester HydrolasesProtein BindingRNA InterferenceTime-Lapse ImagingAurora Kinase BCell Cycle ProteinsKNSTRN protein, humanMicrotubule-Associated ProteinsPhosphoric Monoester HydrolasesSPAG5 protein, human

Identifiers

PMID28751710
PMCPMC5532248

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Registered trials

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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.