Evidence map›Paper›PMID 24133141›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Cell-cycle regulation of formin-mediated actin cable assembly.

Yansong Miao, Catherine C L Wong, Vito Mennella, Alphée Michelot, David A Agard, Liam J Holt, John R Yates, David G Drubin

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  7. Orchestrated actin nucleation by theThe Journal of biological chemistry · 2020
    Article
  8. Review
  9. Article
  10. Review
  11. Genetically inspired in vitro reconstitution ofMolecular biology of the cell · 2020
    Article
  12. Article
  13. Connections between the cell cycle, cell adhesion and the cytoskeleton.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Yansong MiaoDepartment of Molecular and Cell Biology, University of California, Berkeley, CA 94720.
Catherine C L Wong
Vito Mennella
Alphée Michelot
David A Agard
Liam J Holt
John R Yates
David G Drubin
University of California, Berkeley · USScripps Research Institute · USUniversity of California, San Francisco · US

Funding

TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI MACCOSS, MICHAEL · 2012 to 2021
$20.7M
Nikon confocal system for improved spatio-dynamic analysis of endocytic trafficking eventsR35GM118149 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DAVID G DRUBIN · 2016 to 2026
$12.0M
Microtubule Nucleation: Structure & MechanismR01GM031627 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AGARD, DAVID A. · 1985 to 2016
$6.1M
Molecular Analysis of the Yeast Actin CytoskeletonR37GM042759 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DRUBIN, DAVID G · 2006 to 2015
$4.0M
Structure & Mechanism: microtubule nucleation, centrosomes, phage cytoskeletonR35GM118099 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AGARD, DAVID A. · 2016 to 2022
$3.6M
MOLECULAR ANALYSIS OF THE YEAST ACTIN CYTOSKELETONR01GM042759 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DRUBIN, DAVID G. · 1989 to 2005
$1.6M
Howard Hughes Medical InstituteNIGMS NIH HHS P41 GM103533NIGMS NIH HHS R01 GM031627NIGMS NIH HHS R01 GM042759NIGMS NIH HHS R01 GM42759NIGMS NIH HHS R35 GM118099NIGMS NIH HHS R35 GM118149NIGMS NIH HHS R37 GM042759
6 · The paper itself

Abstract

Assembly of appropriately oriented actin cables nucleated by formin proteins is necessary for many biological processes in diverse eukaryotes. However, compared with knowledge of how nucleation of dendritic actin filament arrays by the actin-related protein-2/3 complex is regulated, the in vivo regulatory mechanisms for actin cable formation are less clear. To gain insights into mechanisms for regulating actin cable assembly, we reconstituted the assembly process in vitro by introducing microspheres functionalized with the C terminus of the budding yeast formin Bni1 into extracts prepared from yeast cells at different cell-cycle stages. EM studies showed that unbranched actin filament bundles were reconstituted successfully in the yeast extracts. Only extracts enriched in the mitotic cyclin Clb2 were competent for actin cable assembly, and cyclin-dependent kinase 1 activity was indispensible. Cyclin-dependent kinase 1 activity also was found to regulate cable assembly in vivo. Here we present evidence that formin cell-cycle regulation is conserved in vertebrates. The use of the cable-reconstitution system to test roles for the key actin-binding proteins tropomyosin, capping protein, and cofilin provided important insights into assembly regulation. Furthermore, using mass spectrometry, we identified components of the actin cables formed in yeast extracts, providing the basis for comprehensive understanding of cable assembly and regulation.

Indexed as

Actin CytoskeletonBlotting, WesternCDC2 Protein KinaseCell CycleImage Processing, Computer-AssistedImaging, Three-DimensionalMass SpectrometryMicrofilament ProteinsMicroscopy, Electron, TransmissionMicroscopy, FluorescenceMicrospheresPolymerizationSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsBni1 protein, S cerevisiaeCDC2 Protein KinaseMicrofilament ProteinsSaccharomyces cerevisiae Proteinsactin nucleationCdk1three-dimensional structured-illumination microscopy

Identifiers

PMID24133141
PMCPMC3839727
OpenAlexW2027156887

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.