Evidence map›Paper›PMID 19741097›Full record

ArticleMolecular biology of the cell2009

Myosin Vc is a molecular motor that functions in secretory granule trafficking.

Damon T Jacobs, Roberto Weigert, Kyle D Grode, Julie G Donaldson, Richard E Cheney

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Molecular features of Myosin F adapted for driving actin flows inbioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. NeutrophilFrontiers in cardiovascular medicine · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Measurement of Exocytosis in Genetically Manipulated Mast Cells.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 3 institutions in 1 country.

Damon T JacobsDepartment of Cell and Molecular Physiology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Roberto Weigert
Kyle D Grode
Julie G Donaldson
Richard E Cheney
University of North Carolina at Chapel Hill · USNational Institute of Dental and Craniofacial Research · USNational Institutes of Health · US

Funding

Molecular Mechanisms regulating membrane trafficking in salivary glandsZIADE000717 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI WEIGERT, ROBERTO · 2009 to 2015
$9.2M
Pathways and mechanisms of clathrin-independent endocytosisZIAHL006060 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DONALDSON, JULIE G · 2010 to 2018
$5.7M
Myosin-X: A Novel Myosin with PH DomainsR01DC003299 · NIDCD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHENEY, RICHARD E · 2002 to 2017
$4.4M
Arf GTP-binding proteins and membrane trafficZIAHL000517 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DONALDSON, JULIE G · 2009 to 2016
$2.6M
MYOSIN-X A NOVEL MYOSIN WITH PH DOMAINSR29DC003299 · NIDCD · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI CHENEY, RICHARD E · 1997 to 2001
$202k
NIDCD NIH HHS DC03299NIDCD NIH HHS R01 DC003299NIDCD NIH HHS R29 DC003299
6 · The paper itself

Abstract

Class V myosins are actin-based motor proteins that have critical functions in organelle trafficking. Of the three class V myosins expressed in mammals, relatively little is known about Myo5c except that it is abundant in exocrine tissues. Here we use MCF-7 cells to identify the organelles that Myo5c associates with, image the dynamics of Myo5c in living cells, and test the functions of Myo5c. Endogenous Myo5c localizes to two distinct compartments: small puncta and slender tubules. Myo5c often exhibits a highly polarized distribution toward the leading edge in migrating cells and is clearly distinct from the Myo5a or Myo5b compartments. Imaging with GFP-Myo5c reveals that Myo5c puncta move slowly (approximately 30 nm/s) and microtubule independently, whereas tubules move rapidly (approximately 440 nm/s) and microtubule dependently. Myo5c puncta colocalize with secretory granule markers such as chromogranin A and Rab27b, whereas Myo5c tubules are labeled by Rab8a. TIRF imaging indicates that the granules can be triggered to undergo secretion. To test if Myo5c functions in granule trafficking, we used the Myo5c tail as a dominant negative and found that it dramatically perturbs the distribution of granule markers. These results provide the first live-cell imaging of Myo5c and indicate that Myo5c functions in secretory granule trafficking.

Indexed as

AnimalsCell LineChromogranin AHumansImmunohistochemistryMolecular Motor ProteinsMyosin Heavy ChainsMyosinsMyosin Type VNeuropeptide YNocodazoleRecombinant Fusion ProteinsSecretory VesiclesTubulin ModulatorsChromogranin AMolecular Motor ProteinsMYO5A protein, humanMyo5b protein, ratMYO5C protein, humanMyosin Heavy ChainsMyosinsMyosin Type VNeuropeptide YNocodazoleRecombinant Fusion ProteinsTubulin Modulators

Identifiers

PMID19741097
PMCPMC2770936
OpenAlexW2129118202

What OpenQuestion holds

Textmetadata
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.