Evidence map›Paper›PMID 23870126›Full record

ArticleCell2013

Marking and measuring single microtubules by PRC1 and kinesin-4.

Radhika Subramanian, Shih-Chieh Ti, Lei Tan, Seth A Darst, Tarun M Kapoor

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Cell, 2013. 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 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

104 citing papers in PubMed, 176 citations in OpenAlex.

  1. Article
  2. Microtubule Engagement by the WD40-Containing Tail of Kinesin-4 KIF21B.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. The kinesin-4 protein KIF27 forms a cytoskeletal scaffold at the transition zone to promote motile cilia structural integrity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Mechanism and regulation of kinesin motors.Nature reviews. Molecular cell biology · 2025
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

44 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Radhika SubramanianLaboratory of Chemistry and Cell Biology, The Rockefeller University, 1230 York Avenue, New York, NY 10065, USA.
Shih-Chieh Ti
Lei Tan
Seth A Darst
Tarun M Kapoor
Rockefeller University · US

Funding

Motor Protein Dynamics and Mitotic MechanismsR01GM065933 · NIGMS · ROCKEFELLER UNIVERSITY · PI KAPOOR, TARUN M. · 2002 to 2018
$6.7M
UPGRADE OF IN-HOUSE X-RAY DIFFRACTION EQUIPMENT: STRUCTURAL BIOLOGYS10RR022321 · NCRR · ROCKEFELLER UNIVERSITY · PI DARST, SETH A. · 2006 to 2006
$330k
Asymmetric flow FFF and Composition Gradient/Light Scattering SystemS10RR023748 · NCRR · YALE UNIVERSITY · PI FOLTA-STOGNIEW, EWA JOANNA · 2007 to 2007
$271k
NCRR NIH HHS 1S10RR022321-01NCRR NIH HHS 1S10RR023748-01NCRR NIH HHS S10 RR022321NCRR NIH HHS S10 RR023748NIGMS NIH HHS GM065933NIGMS NIH HHS R01 GM065933
6 · The paper itself

Abstract

Error-free cell division depends on the assembly of the spindle midzone, a specialized array of overlapping microtubules that emerges between segregating chromosomes during anaphase. The molecular mechanisms by which a subset of dynamic microtubules from the metaphase spindle are selected and organized into a stable midzone array are poorly understood. Here, we show using in vitro reconstitution assays that PRC1 and kinesin-4, two microtubule-associated proteins required for midzone assembly, can tag microtubule plus ends. Remarkably, the size of these tags is proportional to filament length. We determine the crystal structure of the PRC1 homodimer and map the protein-protein interactions needed for tagging microtubule ends. Importantly, length-dependent microtubule plus-end-tagging by PRC1 is also observed in dividing cells. Our findings suggest how biochemically similar microtubules can be differentially marked, based on length, for selective regulation during the formation of specialized arrays, such as those required for cytokinesis.

Indexed as

Amino Acid SequenceCell Cycle ProteinsCrystallography, X-RayCytokinesisDimerizationHumansKinesinsMicrotubulesModels, MolecularMolecular Sequence DataSequence AlignmentCell Cycle ProteinsKIF4A protein, humanKinesinsPRC1 protein, human

Identifiers

PMID23870126
PMCPMC3761943
OpenAlexW2089248474

What OpenQuestion holds

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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.