Evidence map›Paper›PMID 26394140›Full record

ArticlePLoS genetics2015

RAB-10-Dependent Membrane Transport Is Required for Dendrite Arborization.

Wei Zou, Smita Yadav, Laura DeVault, Yuh Nung Jan, David R Sherwood

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. 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 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.0field-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

57 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. EHBP1 Is Critically Involved in the Dendritic Arbor Formation and Is Coupled to Factors Promoting Actin Filament Formation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Wei ZouDepartment of Biology, Duke University, Durham, North Carolina, United States of America.
Smita YadavHoward Hughes Medical Institute, Department of Physiology, University of California, San Francisco, San Francisco, California, United States of America.
Laura DeVaultHoward Hughes Medical Institute, Department of Physiology, University of California, San Francisco, San Francisco, California, United States of America.
Yuh Nung JanHoward Hughes Medical Institute, Department of Physiology, University of California, San Francisco, San Francisco, California, United States of America.
David R SherwoodDepartment of Biology, Duke University, Durham, North Carolina, United States of America.
Howard Hughes Medical Institute · USDuke University · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Genetic Analysis of Cell Invasion through Basement MembranesR01GM079320 · NIGMS · DUKE UNIVERSITY · PI SHERWOOD, DAVID R · 2007 to 2015
$2.8M
Understanding How Invadosomes Breach Basement Membrane In VivoR01GM100083 · NIGMS · DUKE UNIVERSITY · PI SHERWOOD, DAVID R · 2012 to 2015
$1.1M
NIGMS NIH HHS GM079320NIGMS NIH HHS R01 GM079320NIGMS NIH HHS R01 GM100083NIH HHS P40 OD010440
6 · The paper itself

Abstract

Formation of elaborately branched dendrites is necessary for the proper input and connectivity of many sensory neurons. Previous studies have revealed that dendritic growth relies heavily on ER-to-Golgi transport, Golgi outposts and endocytic recycling. How new membrane and associated cargo is delivered from the secretory and endosomal compartments to sites of active dendritic growth, however, remains unknown. Using a candidate-based genetic screen in C. elegans, we have identified the small GTPase RAB-10 as a key regulator of membrane trafficking during dendrite morphogenesis. Loss of rab-10 severely reduced proximal dendritic arborization in the multi-dendritic PVD neuron. RAB-10 acts cell-autonomously in the PVD neuron and localizes to the Golgi and early endosomes. Loss of function mutations of the exocyst complex components exoc-8 and sec-8, which regulate tethering, docking and fusion of transport vesicles at the plasma membrane, also caused proximal dendritic arborization defects and led to the accumulation of intracellular RAB-10 vesicles. In rab-10 and exoc-8 mutants, the trans-membrane proteins DMA-1 and HPO-30, which promote PVD dendrite stabilization and branching, no longer localized strongly to the proximal dendritic membranes and instead were sequestered within intracellular vesicles. Together these results suggest a crucial role for the Rab10 GTPase and the exocyst complex in controlling membrane transport from the secretory and/or endosomal compartments that is required for dendritic growth.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDendritesEndocytosisEndoplasmic ReticulumEndosomesGolgi ApparatusMembrane ProteinsMembrane Transport ModulatorsNeuronal Plasticityrab GTP-Binding ProteinsSensory Receptor CellsCaenorhabditis elegans ProteinsDMA-1 protein, C elegansMembrane ProteinsMembrane Transport ModulatorsRAB-10 protein, C elegansrab GTP-Binding Proteins

Identifiers

PMID26394140
PMCPMC4578882
OpenAlexW1952319206

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.