Evidence map›Paper›PMID 31320392›Full record

ArticleThe Journal of cell biology2019

Hook3 is a scaffold for the opposite-polarity microtubule-based motors cytoplasmic dynein-1 and KIF1C.

Agnieszka A Kendrick, Andrea M Dickey, William B Redwine, Phuoc Tien Tran, Laura Pontano Vaites, Monika Dzieciatkowska, J Wade Harper, Samara L Reck-Peterson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
5.5field-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

57 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. AnbioRxiv : the preprint server for biology · 2026
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  12. CCSer2 gates dynein activity at the cell periphery.The Journal of cell biology · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Mechanism and regulation of kinesin motors.Nature reviews. Molecular cell biology · 2025
    Review
  17. Article
  18. Article
  19. CCSer2 gates dynein activity at the cell periphery.bioRxiv : the preprint server for biology · 2024
    Article
  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

8 authors at 4 institutions in 1 country.

Agnieszka A KendrickDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA.ORCID 0000-0003-3254-4582
Andrea M Dickey *Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA.
William B Redwine *Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA.ORCID 0000-0001-6342-7253
Phuoc Tien TranDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA.ORCID 0000-0003-3354-5907
Laura Pontano VaitesDepartment of Cell Biology, Harvard Medical School, Boston, MA.
Monika DzieciatkowskaDepartment of Biochemistry and Molecular Genetics, University of Colorado Denver, Aurora, CO.
J Wade HarperDepartment of Cell Biology, Harvard Medical School, Boston, MA.ORCID 0000-0002-6944-7236
Samara L Reck-PetersonDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA sreckpeterson@ucsd.edu.ORCID 0000-0002-1553-465X
Harvard University · USUniversity of California San Diego · USHoward Hughes Medical Institute · USUniversity of Colorado Denver · US

Funding

Endolysosomal Proteome Landscapes Through the Lens of Neurodegenerative Risk AllelesR01NS110395 · NINDS · HARVARD MEDICAL SCHOOL · PI JEFFREY W HARPER · 2018 to 2026
$4.1M
Systematic discovery and functional analysis of the PARKIN modified proteomeR37NS083524 · NINDS · HARVARD MEDICAL SCHOOL · PI HARPER, JEFFREY W · 2013 to 2019
$3.0M
Cellular control of microtubule-based transport.R01GM121772 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RECK-PETERSON, SAMARA L · 2017 to 2020
$1.6M
Mechanism and function of the kinesin-3, KIF1CF32GM125224 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KENDRICK, AGNIESZKA ANASTAZJA · 2018 to 2018
$21k
NIGMS NIH HHS F32 GM125224NIGMS NIH HHS R01 GM121772NINDS NIH HHS R01 NS110395NINDS NIH HHS R37 NS083524
6 · The paper itself

Abstract

The unidirectional and opposite-polarity microtubule-based motors, dynein and kinesin, drive long-distance intracellular cargo transport. Cellular observations suggest that opposite-polarity motors may be coupled. We recently identified an interaction between the cytoplasmic dynein-1 activating adaptor Hook3 and the kinesin-3 KIF1C. Here, using in vitro reconstitutions with purified components, we show that KIF1C and dynein/dynactin can exist in a complex scaffolded by Hook3. Full-length Hook3 binds to and activates dynein/dynactin motility. Hook3 also binds to a short region in the "tail" of KIF1C, but unlike dynein/dynactin, this interaction does not activate KIF1C. Hook3 scaffolding allows dynein to transport KIF1C toward the microtubule minus end, and KIF1C to transport dynein toward the microtubule plus end. In cells, KIF1C can recruit Hook3 to the cell periphery, although the cellular role of the complex containing both motors remains unknown. We propose that Hook3's ability to scaffold dynein/dynactin and KIF1C may regulate bidirectional motility, promote motor recycling, or sequester the pool of available dynein/dynactin activating adaptors.

Indexed as

Cell Line, TumorDyneinsHumansKinesinsMicrotubule-Associated ProteinsMicrotubulesDyneinshook3 protein, humanKIF1C protein, humanKinesinsMicrotubule-Associated Proteins

Identifiers

PMID31320392
PMCPMC6719453
OpenAlexW2963588125

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.