Evidence map›Paper›PMID 28759579›Full record

ArticlePLoS genetics2017

Dynactin binding to tyrosinated microtubules promotes centrosome centration in C. elegans by enhancing dynein-mediated organelle transport.

Daniel J Barbosa, Joana Duro, Bram Prevo, Dhanya K Cheerambathur, Ana X Carvalho, Reto Gassmann

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.1field-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

26 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  8. Article
  9. Article
  10. The Expression and Function of Tubulin Isotypes inFrontiers in cell and developmental biology · 2022
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Activation and Regulation of Cytoplasmic Dynein.Trends in biochemical sciences · 2020
    Review
  16. Article
  17. Article
  18. Cytoskeleton Force Exertion in Bulk Cytoplasm.Frontiers in cell and developmental biology · 2020
    Review
  19. Review
  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

6 authors at 2 institutions in 2 countries.

Daniel J BarbosaInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Joana DuroInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Bram PrevoLudwig Institute for Cancer Research/Dept of Cellular & Molecular Medicine UCSD, La Jolla, CA, United States of America.
Dhanya K CheerambathurLudwig Institute for Cancer Research/Dept of Cellular & Molecular Medicine UCSD, La Jolla, CA, United States of America.
Ana X CarvalhoInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.ORCID http://orcid.org/0000-0002-2256-7134
Reto GassmannInstituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.ORCID http://orcid.org/0000-0002-0360-2977
Universidade do Porto · PTLudwig Cancer Research · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

The microtubule-based motor dynein generates pulling forces for centrosome centration and mitotic spindle positioning in animal cells. How the essential dynein activator dynactin regulates these functions of the motor is incompletely understood. Here, we dissect the role of dynactin's microtubule binding activity, located in the p150 CAP-Gly domain and an adjacent basic patch, in the C. elegans zygote. Analysis of p150 mutants engineered by genome editing suggests that microtubule tip tracking of dynein-dynactin is dispensable for targeting the motor to the cell cortex and for generating robust cortical pulling forces. Instead, mutations in p150's CAP-Gly domain inhibit cytoplasmic pulling forces responsible for centration of centrosomes and attached pronuclei. The centration defects are mimicked by mutations of α-tubulin's C-terminal tyrosine, and both p150 CAP-Gly and tubulin tyrosine mutants decrease the frequency of early endosome transport from the cell periphery towards centrosomes during centration. Our results suggest that p150 GAP-Gly domain binding to tyrosinated microtubules promotes initiation of dynein-mediated organelle transport in the dividing one-cell embryo, and that this function of p150 is critical for generating cytoplasmic pulling forces for centrosome centration.

Indexed as

AnimalsCaenorhabditis elegansCell NucleusCentrosomeDynactin ComplexDyneinsGene EditingMicrotubule-Associated ProteinsMicrotubulesProtein BindingProtein DomainsSpindle ApparatusTubulinTyrosineZygoteDynactin ComplexDyneinsMicrotubule-Associated ProteinsTubulinTyrosine

Identifiers

PMID28759579
PMCPMC5552355
OpenAlexW2953106150

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.