Evidence map›Paper›PMID 17676955›Full record

ArticlePLoS genetics2007

Dynein modifiers in C. elegans: light chains suppress conditional heavy chain mutants.

Sean M O'Rourke, Marc D Dorfman, J Clayton Carter, Bruce Bowerman

Open access · goldAbstract readComparative Study
In one paragraph

Article in PLoS genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

63 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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  12. The conserved autoimmune-disease risk geneProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. A Series of Tubes: TheJournal of developmental biology · 2020
    Review
  15. Lysosomal activity regulatesProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  16. Alanine tRNAs Translate Environment Into Behavior inFrontiers in cell and developmental biology · 2020
    Article
  17. Review
  18. A Model of Hereditary Sensory and Autonomic Neuropathy Type 1 Reveals a Role of Glycosphingolipids in Neuronal Polarity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  19. Article
  20. Mechanisms of suppression: The wiring of genetic resilience.BioEssays : news and reviews in molecular, cellular and developmental biology · 2017
    Review

3 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Sean M O'RourkeInstitute of Molecular Biology, University of Oregon, Eugene, Oregon, United States of America. seanor@molbio.uoregon.edu
Marc D Dorfman
J Clayton Carter
Bruce Bowerman
University of Oregon · US

Funding

DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007348 · NICHD · UNIVERSITY OF OREGON · PI Chris Q Doe, KRYN STANKUNAS · 1989 to 2026
$6.8M
Mitotic Spindle Assembly & Function in C. elegans - Equipment SupplementR01GM049869 · NIGMS · UNIVERSITY OF OREGON · PI BOWERMAN, BRUCE A · 1994 to 2019
$6.5M
NICHD NIH HHS T32 HD007348NIGMS NIH HHS GM049869NIGMS NIH HHS R01 GM049869
6 · The paper itself

Abstract

Cytoplasmic dynein is a microtubule-dependent motor protein that functions in mitotic cells during centrosome separation, metaphase chromosome congression, anaphase spindle elongation, and chromosome segregation. Dynein is also utilized during interphase for vesicle transport and organelle positioning. While numerous cellular processes require cytoplasmic dynein, the mechanisms that target and regulate this microtubule motor remain largely unknown. By screening a conditional Caenorhabditis elegans cytoplasmic dynein heavy chain mutant at a semipermissive temperature with a genome-wide RNA interference library to reduce gene functions, we have isolated and characterized twenty dynein-specific suppressor genes. When reduced in function, these genes suppress dynein mutants but not other conditionally mutant loci, and twelve of the 20 specific suppressors do not exhibit sterile or lethal phenotypes when their function is reduced in wild-type worms. Many of the suppressor proteins, including two dynein light chains, localize to subcellular sites that overlap with those reported by others for the dynein heavy chain. Furthermore, knocking down any one of four putative dynein accessory chains suppresses the conditional heavy chain mutants, suggesting that some accessory chains negatively regulate heavy chain function. We also identified 29 additional genes that, when reduced in function, suppress conditional mutations not only in dynein but also in loci required for unrelated essential processes. In conclusion, we have identified twenty genes that in many cases are not essential themselves but are conserved and when reduced in function can suppress conditionally lethal C. elegans cytoplasmic dynein heavy chain mutants. We conclude that conserved but nonessential genes contribute to dynein function during the essential process of mitosis.

Indexed as

AnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCaenorhabditis elegans ProteinsCarrier ProteinsCytoplasmCytoplasmic DyneinsDrosophila ProteinsDyneinsProtein SubunitsRepressor ProteinsCaenorhabditis elegans ProteinsCarrier ProteinsCytoplasmic DyneinsDHC-1 protein, C elegansDrosophila ProteinsDyneinsProtein SubunitsRepressor Proteins

Identifiers

PMID17676955
PMCPMC1937013
OpenAlexW2016427041

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.