Evidence map›Paper›PMID 16291862›Full record

ArticleMolecular biology of the cell2006

Arp10p is a pointed-end-associated component of yeast dynactin.

Sean W Clark, Mark D Rose

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. VezA/vezatin facilitates proper assembly of the dynactin complex in vivo.bioRxiv : the preprint server for biology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The evolution of the cytoskeleton.The Journal of cell biology · 2011
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Dynactin function in mitotic spindle positioning.Traffic (Copenhagen, Denmark) · 2008
    Article
  15. Article
  16. Article
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

2 authors at 1 institution in 1 country.

Sean W ClarkDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Mark D Rose
Princeton University · US

Funding

Mechanisms of Nuclear and Cell Fusion in YeastR01GM037739 · NIGMS · PRINCETON UNIVERSITY · PI ROSE, MARK DAVID · 1987 to 2016
$7.4M
ONCOLOGY: MOLECULAR BASIS OF CANCERT32CA009528 · NCI · PRINCETON UNIVERSITY · PI BROACH, JAMES R. · 1985 to 2010
$5.9M
GENETICS OF THE YEAST MICROTUBULE ORGANIZING CENTERR01GM052526 · NIGMS · PRINCETON UNIVERSITY · PI ROSE, MARK DAVID · 1995 to 2003
$1.0M
NCI NIH HHS CA-09528NCI NIH HHS T32 CA009528NIGMS NIH HHS GM-37739NIGMS NIH HHS GM-52526NIGMS NIH HHS R01 GM037739NIGMS NIH HHS R01 GM052526
6 · The paper itself

Abstract

In metazoans, dynein-dependent vesicle transport is mediated by dynactin, containing an actin-related protein, Arp1p, together with a cargo-selection complex containing a second actin-related protein, Arp11. Paradoxically, in budding yeast, models of dynactin function imply an interaction with membranes, whereas the lack of microtubule-based vesicle transport implies the absence of a cargo-selection complex. Using both genetic and biochemical approaches, we demonstrate that Arp10p is the functional yeast homologue of Arp11, suggesting the possible existence of a pointed-end complex in yeast. Specifically, Arp10p interacts with Arp1p and other dynactin subunits and is dependent on Arp1p for stability. Conversely, Arp10p stabilizes the dynactin complex by association with the Arp1p filament pointed end. Using a novel hRAS-Arp1p one-hybrid assay, we show that Arp1p associates with the plasma membrane dependent on dynactin subunits, but independent of dynein, and sensitive to cell wall damage. We directly show the association of Arp1p with not only the plasma membrane but also with a less dense membrane fraction. Based on the hRAS-Arp1p assay, loss of Arp10p enhances the apparent association of dynactin with the plasma membrane and suppresses the loss of signaling conferred by cell wall damage.

Indexed as

Cell MembraneCell WallCytoskeletonDynactin ComplexFungal ProteinsHumansMicrofilament ProteinsMicrotubule-Associated ProteinsModels, MolecularProtein ConformationProtein Interaction Mappingras ProteinsRecombinant Fusion ProteinsSaccharomycetalesDynactin ComplexFungal ProteinsMicrofilament ProteinsMicrotubule-Associated Proteinsras ProteinsRecombinant Fusion Proteins

Identifiers

PMID16291862
PMCPMC1356584
OpenAlexW2117962007

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.