Evidence map›Paper›PMID 16394096›Full record

ArticleMolecular biology of the cell2006

Actin-based motility during endocytosis in budding yeast.

Kyoungtae Kim, Brian J Galletta, Kevin O Schmidt, Fanny S Chang, Kendall J Blumer, John A Cooper

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 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

35 citing papers in PubMed, 62 citations in OpenAlex.

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  17. Ultrastructural imaging of endocytic sites in Saccharomyces cerevisiae by transmission electron microscopy and immunolabeling.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada · 2013
    Article
  18. Ultrastructural dynamics of proteins involved in endocytic budding.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Kyoungtae KimDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Brian J Galletta
Kevin O Schmidt
Fanny S Chang
Kendall J Blumer
John A Cooper
Washington University in St. Louis · US

Funding

MECHANISM &REGULATION OF RECEPTOR G PROTEIN SIGNALINGR01GM044592 · NIGMS · WASHINGTON UNIVERSITY · PI BLUMER, KENDALL J · 1990 to 2017
$7.5M
Molecular Mechanisms in Actin Assembly &Cell MotilityR01GM038542 · NIGMS · WASHINGTON UNIVERSITY · PI COOPER, JOHN A · 1989 to 2013
$7.4M
The Function of Dynein in Budding YeastR01GM047337 · NIGMS · WASHINGTON UNIVERSITY · PI COOPER, JOHN A · 1993 to 2009
$2.6M
NIGMS NIH HHS GM-38542NIGMS NIH HHS GM-47337NIGMS NIH HHS R01 GM038542NIGMS NIH HHS R01 GM044592NIGMS NIH HHS R01 GM047337
6 · The paper itself

Abstract

Actin assembly nucleated by Arp2/3 complex has been implicated in the formation and movement of endocytic vesicles. The dendritic nucleation model has been proposed to account for Arp2/3-mediated actin assembly and movement. Here, we explored the model by examining the role of capping protein in vivo, with quantitative tracking analysis of fluorescence markers for different stages of endocytosis in yeast. Capping protein was most important for the initial movement of endocytic vesicles away from the plasma membrane, which presumably corresponds to vesicle scission and release. The next phase of endosome movement away from the plasma membrane was also affected, but less so. The results are consistent with the dendritic nucleation model's prediction of capping protein as important for efficient actin assembly and force production. In contrast, the movement of late-stage endocytic vesicles, traveling through the cytoplasm en route to the vacuole, did not depend on capping protein. The movement of these vesicles was found previously to depend on Lsb6, a WASp interactor, whereas Lsb6 was found here to be dispensable for early endosome movement. Thus, the molecular requirements for Arp2/3-based actin assembly differ in early versus later stages of endocytosis. Finally, acute loss of actin cables led to increased patch motility.

Indexed as

Cell MovementActin Capping ProteinsActinsBiomarkersCell MembraneEndocytosisFungal ProteinsPolymersPyridinium CompoundsQuaternary Ammonium CompoundsRecombinant Fusion ProteinsSaccharomycetalesTime FactorsActin Capping ProteinsActinsBiomarkersFM 4-64Fungal ProteinsPolymersPyridinium CompoundsQuaternary Ammonium CompoundsRecombinant Fusion Proteins

Identifiers

PMID16394096
PMCPMC1382323
OpenAlexW2096800682

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.