Evidence map›Paper›PMID 22334675›Full record

ArticleThe Journal of biological chemistry2012

Multiple forms of Spire-actin complexes and their functional consequences.

Christine K Chen, Michael R Sawaya, Martin L Phillips, Emil Reisler, Margot E Quinlan

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. 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
–field-weighted citation impact
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.

  1. Article
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  11. Article
  12. Article
  13. In vitro studies of actin filament and network dynamics.Current opinion in cell biology · 2013
    Review
  14. Article
  15. Structure of the formin-interaction domain of the actin nucleation-promoting factor Bud6.Proceedings of the National Academy of Sciences of the United States of America · 2012
    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

5 authors.

Christine K ChenDepartment of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095.
Michael R SawayaDepartment of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095.
Martin L PhillipsDepartment of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095.
Emil ReislerDepartment of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095; Molecular Biology Institute, University of California Los Angeles, Los Angeles, California 90095.
Margot E QuinlanDepartment of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095; Molecular Biology Institute, University of California Los Angeles, Los Angeles, California 90095. Electronic address: margot@chem.ucla.edu.

Funding

Dynamic Events in Myosin and Actin and Their FunctionR01GM077190 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REISLER, EMIL · 2006 to 2020
$6.2M
Collaboration between actin nucleators - Spire and CappuccinoR01GM096133 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI QUINLAN, MARGOT E · 2011 to 2024
$4.1M
NIGMS NIH HHS GM077190NIGMS NIH HHS R01 GM077190NIGMS NIH HHS R01 GM096133
6 · The paper itself

Abstract

Spire is a WH2 domain-containing actin nucleator essential for establishing an actin mesh during oogenesis. In vitro, in addition to nucleating filaments, Spire can sever them and sequester actin monomers. Understanding how Spire is capable of these disparate functions and which are physiologically relevant is an important goal. To study severing, we examined the effect of Drosophila Spire on preformed filaments in bulk and single filament assays. We observed rapid depolymerization of actin filaments by Spire, which we conclude is largely due to its sequestration activity and enhanced by its weak severing activity. We also studied the solution and crystal structures of Spire-actin complexes. We find structural and functional differences between constructs containing four WH2 domains (Spir-ABCD) and two WH2 domains (Spir-CD) that may provide insight into the mechanisms of nucleation and sequestration. Intriguingly, we observed lateral interactions between actin monomers associated with Spir-ABCD, suggesting that the structures built by these four tandem WH2 domains are more complex than originally imagined. Finally, we propose that Spire-actin mixtures contain both nuclei and sequestration structures.

Indexed as

Actin CytoskeletonActinsAnimalsCrystallography, X-RayDrosophila melanogasterDrosophila ProteinsMicrofilament ProteinsMultiprotein ComplexesProtein Structure, QuaternaryProtein Structure, TertiaryStructure-Activity RelationshipActinsDrosophila ProteinsMicrofilament ProteinsMultiprotein Complexesspir protein, Drosophila

Identifiers

PMID22334675
PMCPMC3323035

What OpenQuestion holds

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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.