Evidence map›Paper›PMID 36409768›Full record

ArticlePLoS genetics2022

The ANC-1 (Nesprin-1/2) organelle-anchoring protein functions through mitochondria to polarize axon growth in response to SLT-1.

Nathan C Fischer, Vladislav Friedman, Miguel A Martinez-Reyes, Hongyan Hao, Tamjid A Chowdhury, Daniel A Starr, Christopher C Quinn

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Non-transport functions of motor proteins in corticogenesis.Frontiers in cell and developmental biology · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Autism candidate genebioRxiv : the preprint server for biology · 2024
    Article
  9. 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

7 authors at 2 institutions in 1 country.

Nathan C FischerDepartment of Biological Sciences, University of Wisconsin-Milwaukee; Milwaukee, Wisconsin, United States of America.
Vladislav FriedmanDepartment of Biological Sciences, University of Wisconsin-Milwaukee; Milwaukee, Wisconsin, United States of America.ORCID 0000-0002-5567-2520
Miguel A Martinez-ReyesDepartment of Biological Sciences, University of Wisconsin-Milwaukee; Milwaukee, Wisconsin, United States of America.
Hongyan HaoDepartment of Molecular and Cellular Biology, University of California, Davis, California, United States of America.
Tamjid A ChowdhuryDepartment of Biological Sciences, University of Wisconsin-Milwaukee; Milwaukee, Wisconsin, United States of America.
Daniel A StarrDepartment of Molecular and Cellular Biology, University of California, Davis, California, United States of America.
Christopher C QuinnDepartment of Biological Sciences, University of Wisconsin-Milwaukee; Milwaukee, Wisconsin, United States of America.ORCID 0000-0002-0144-3423
University of Wisconsin–Milwaukee · USUniversity of California, Davis · US

Funding

Mechanisms of Nuclear MigrationR35GM134859 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DANIEL A STARR · 2020 to 2026
$2.8M
Investigation of how axon development is disrupted by the autism-causing Timothy syndrome mutation.R01MH119157 · NIMH · UNIVERSITY OF WISCONSIN MILWAUKEE · PI QUINN, CHRISTOPHER C · 2019 to 2023
$1.9M
NIGMS NIH HHS R35 GM134859NIMH NIH HHS R01 MH119157
6 · The paper itself

Abstract

A family of giant KASH proteins, including C. elegans ANC-1 and mammalian Nesprin-1 and -2, are involved in organelle anchoring and are associated with multiple neurodevelopmental disorders including autism, bipolar disorder, and schizophrenia. However, little is known about how these proteins function in neurons. Moreover, the role of organelle anchoring in axon development is poorly understood. Here, we report that ANC-1 functions with the SLT-1 extracellular guidance cue to polarize ALM axon growth. This role for ANC-1 is specific to its longer ANC-1A and ANC-1C isoforms, suggesting that it is mechanistically distinct from previously described roles for ANC-1. We find that ANC-1 is required for the localization of a cluster of mitochondria to the base of the proximal axon. Furthermore, genetic and pharmacological studies indicate that ANC-1 functions with mitochondria to promote polarization of ALM axon growth. These observations reveal a mechanism whereby ANC-1 functions through mitochondria to polarize axon growth in response to SLT-1.

Indexed as

Caenorhabditis elegans ProteinsAnimalsAxonsBoranesCaenorhabditis elegansMammalsMicrofilament ProteinsMitochondriaPropylaminesANC 1ANC-1 protein, C elegansBoranesCaenorhabditis elegans ProteinsMicrofilament ProteinsPropylamines

Identifiers

PMID36409768
PMCPMC9721489
OpenAlexW4309494699

What Socratic 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 Socratic graph.