Evidence map›Paper›PMID 26354976›Full record

ArticleGenetics2015

UNC-16 (JIP3) Acts Through Synapse-Assembly Proteins to Inhibit the Active Transport of Cell Soma Organelles to Caenorhabditis elegans Motor Neuron Axons.

Stacey L Edwards, Logan M Morrison, Rosalina M Yorks, Christopher M Hoover, Soorajnath Boominathan, Kenneth G Miller

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Neuronal lysosomes.Neuroscience letters · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. The Endolysosomal System and Proteostasis: From Development to Degeneration.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Review
  15. Axonal transport and maturation of lysosomes.Current opinion in neurobiology · 2018
    Review
  16. Article
  17. Article
  18. 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

6 authors at 1 institution in 1 country.

Stacey L EdwardsGenetic Models of Disease Laboratory, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104.
Logan M MorrisonGenetic Models of Disease Laboratory, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104.
Rosalina M YorksGenetic Models of Disease Laboratory, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104.
Christopher M HooverGenetic Models of Disease Laboratory, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104.
Soorajnath BoominathanGenetic Models of Disease Laboratory, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104.
Kenneth G MillerGenetic Models of Disease Laboratory, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104 millerk@omrf.org.
Oklahoma Medical Research Foundation · 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
Signaling Pathways that Regulate Synaptic TransmissionR01GM080765 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI MILLER, KENNETH GEORGE · 2007 to 2015
$2.7M
NIGMS NIH HHS R01 GM080765NIGMS NIH HHS R01GM080765NIH HHS P40 OD010440NIH HHS P40OD010440
6 · The paper itself

Abstract

The conserved protein UNC-16 (JIP3) inhibits the active transport of some cell soma organelles, such as lysosomes, early endosomes, and Golgi, to the synaptic region of axons. However, little is known about UNC-16's organelle transport regulatory function, which is distinct from its Kinesin-1 adaptor function. We used an unc-16 suppressor screen in Caenorhabditis elegans to discover that UNC-16 acts through CDK-5 (Cdk5) and two conserved synapse assembly proteins: SAD-1 (SAD-A Kinase), and SYD-2 (Liprin-α). Genetic analysis of all combinations of double and triple mutants in unc-16(+) and unc-16(-) backgrounds showed that the three proteins (CDK-5, SAD-1, and SYD-2) are all part of the same organelle transport regulatory system, which we named the CSS system based on its founder proteins. Further genetic analysis revealed roles for SYD-1 (another synapse assembly protein) and STRADα (a SAD-1-interacting protein) in the CSS system. In an unc-16(-) background, loss of the CSS system improved the sluggish locomotion of unc-16 mutants, inhibited axonal lysosome accumulation, and led to the dynein-dependent accumulation of lysosomes in dendrites. Time-lapse imaging of lysosomes in CSS system mutants in unc-16(+) and unc-16(-) backgrounds revealed active transport defects consistent with the steady-state distributions of lysosomes. UNC-16 also uses the CSS system to regulate the distribution of early endosomes in neurons and, to a lesser extent, Golgi. The data reveal a new and unprecedented role for synapse assembly proteins, acting as part of the newly defined CSS system, in mediating UNC-16's organelle transport regulatory function.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAxonsBiological Transport, ActiveCaenorhabditis elegansCaenorhabditis elegans ProteinsCyclin-Dependent Kinase 5Intercellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsMotor NeuronsOrganellesPhosphoproteinsProtein Serine-Threonine KinasesAdaptor Proteins, Signal TransducingCaenorhabditis elegans ProteinsCyclin-Dependent Kinase 5Intercellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsPhosphoproteinsProtein Serine-Threonine Kinasessad-1 protein, C elegansSTRD-1 protein, C elegansSYD-2 protein, C elegansunc-16 protein, C elegansaxonal transportCaenorhabditis elegansCdk5dyneinJIP3LiprinSAD-A

Identifiers

PMID26354976
PMCPMC4566257
OpenAlexW2178301990

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.