Evidence map›Paper›PMID 31804178›Full record

ArticleeLife2019

Molecular determinants of the Ska-Ndc80 interaction and their influence on microtubule tracking and force-coupling.

Pim J Huis In 't Veld, Vladimir A Volkov, Isabelle D Stender, Andrea Musacchio, Marileen Dogterom

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 citing papers in PubMed.

  1. Structure and function of the outer kinetochore.Nature reviews. Molecular cell 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

5 authors.

Pim J Huis In 't Veld *Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0003-0234-6390
Vladimir A Volkov *Department of Bionanoscience, Faculty of Applied Sciences, Delft University of Technology, Delft, Netherlands.ORCID 0000-0002-5407-3366
Isabelle D StenderDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Andrea MusacchioDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0003-2362-8784
Marileen DogteromDepartment of Bionanoscience, Faculty of Applied Sciences, Delft University of Technology, Delft, Netherlands.ORCID 0000-0002-8803-5261

Funding

Deutsche Forschungsgemeinschaft CRC1093European Commission ERC AdG RECEPIANCE (proposal 669686)European Commission ERC SG MODELCELL (proposal 609822)European Molecular Biology Organization STF7203
6 · The paper itself

Abstract

Errorless chromosome segregation requires load-bearing attachments of the plus ends of spindle microtubules to chromosome structures named kinetochores. How these end-on kinetochore attachments are established following initial lateral contacts with the microtubule lattice is poorly understood. Two microtubule-binding complexes, the Ndc80 and Ska complexes, are important for efficient end-on coupling and may function as a unit in this process, but precise conditions for their interaction are unknown. Here, we report that the Ska-Ndc80 interaction is phosphorylation-dependent and does not require microtubules, applied force, or several previously identified functional determinants including the Ndc80-loop and the Ndc80-tail. Both the Ndc80-tail, which we reveal to be essential for microtubule end-tracking, and Ndc80-bound Ska stabilize microtubule ends in a stalled conformation. Modulation of force-coupling efficiency demonstrates that the duration of stalled microtubule disassembly predicts whether a microtubule is stabilized and rescued by the kinetochore, likely reflecting a structural transition of the microtubule end.

Indexed as

Aurora Kinase BCDC2 Protein KinaseCell Cycle ProteinsChromosomal Proteins, Non-HistoneChromosome SegregationCytoskeletal ProteinsHumansKinetochoresMicrotubule-Associated ProteinsMicrotubulesModels, MolecularPhosphorylationProtein BindingProtein ConformationProtein Interaction Domains and MotifsSequence Analysis, ProteinAURKB protein, humanAurora Kinase BCDC2 Protein KinaseCDK1 protein, humanCell Cycle ProteinsChromosomal Proteins, Non-HistoneCytoskeletal ProteinsMicrotubule-Associated ProteinsNDC80 protein, humanSKA1 protein, humanSKA2 protein, humanSka3 protein, humanSPC24 protein, humanSPC25 protein, humanbiochemistrycell divisionchemical biologyforce-couplinghumankinetochoremicrotubulemolecular biophysicsNdc80Skastructural biology

Identifiers

PMID31804178
PMCPMC6927755

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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.