Evidence map›Paper›PMID 27091402›Full record

ArticleNature communications2016

Tum/RacGAP functions as a switch activating the Pav/kinesin-6 motor.

Li Tao, Barbara Fasulo, Brandt Warecki, William Sullivan

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Proximity labeling reveals novel interactomes in liveDevelopment (Cambridge, England) · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Bio-protocol · 2017
    Article
  14. Article
  15. Anaphase B.Biology · 2016
    Review
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.

Li TaoDepartment of Biology, University of Hawaii at Hilo, 200 West Kawili Street, Hilo, Hawaii 96720, USA.
Barbara FasuloDepartment of Molecular, Cellular and Developmental Biology, University of California, Santa Cruz, California 95064, USA.
Brandt WareckiDepartment of Molecular, Cellular and Developmental Biology, University of California, Santa Cruz, California 95064, USA.
William SullivanDepartment of Molecular, Cellular and Developmental Biology, University of California, Santa Cruz, California 95064, USA.

Funding

CYTOKINESIS IN THE EARLY DROSOPHILA EMBRYOR01GM046409 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI SULLIVAN, WILLIAM T. · 1997 to 2014
$4.7M
Training Program/Molecular/Cell/Developmental BiologyT32GM008646 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI STROME, SUSAN · 1999 to 2018
$3.7M
NIGMS NIH HHS 5 R01 GM046409NIGMS NIH HHS R01 GM046409NIGMS NIH HHS T32 GM008646PHS HHS 5T32GGM008646-17
6 · The paper itself

Abstract

Centralspindlin is essential for central spindle and cleavage furrow formation. Drosophila centralspindlin consists of a kinesin-6 motor (Pav/kinesin-6) and a GTPase-activating protein (Tum/RacGAP). Centralspindlin localization to the central spindle is mediated by Pav/kinesin-6. While Tum/RacGAP has well-documented scaffolding functions, whether it influences Pav/kinesin-6 function is less well-explored. Here we demonstrate that both Pav/kinesin-6 and the centralspindlin complex (co-expressed Pav/Tum) have strong microtubule bundling activity. Centralspindlin also has robust plus-end-directed motility. In contrast, Pav/kinesin-6 alone cannot move microtubules. However, the addition of Tum/RacGAP or a 65 amino acid Tum/RacGAP fragment to Pav/kinesin-6 restores microtubule motility. Further, ATPase assays reveal that microtubule-stimulated ATPase activity of centralspindlin is seven times higher than that of Pav/kinesin-6. These findings are supported by in vivo studies demonstrating that in Tum/RacGAP-depleted S2 Drosophila cells, Pav/kinesin-6 exhibits severely reduced localization to the central spindle and an abnormal concentration at the centrosomes.

Indexed as

Adenosine TriphosphatasesAnimalsBlotting, WesternCell LineCentrosomeDrosophila melanogasterDrosophila ProteinsGTPase-Activating ProteinsKinesinsKineticsMicroscopy, FluorescenceMicrotubule-Associated ProteinsMicrotubulesMolecular Motor ProteinsMultiprotein ComplexesRNA InterferenceAdenosine TriphosphatasesDrosophila ProteinsGTPase-Activating ProteinsKinesinsMicrotubule-Associated ProteinsMolecular Motor ProteinsMultiprotein Complexespav protein, Drosophilatum protein, Drosophila

Identifiers

PMID27091402
PMCPMC4838857

What OpenQuestion holds

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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.