Evidence map›Paper›PMID 26074334›Full record

ReviewCytoskeleton (Hoboken, N.J.)2015

Drosophila comes of age as a model system for understanding the function of cytoskeletal proteins in cells, tissues, and organisms.

Avital A Rodal, Steven J Del Signore, Adam C Martin

Abstract readReview
In one paragraph

Review in Cytoskeleton (Hoboken, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Frontiers in genetics · 2019
    Review
  5. 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

3 authors.

Avital A RodalDepartment of Biology, Brandeis University, Waltham, Massachusetts.
Steven J Del SignoreDepartment of Biology, Brandeis University, Waltham, Massachusetts.
Adam C MartinDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts.

Funding

Quantitative Neuroscience: Tools for Bridging Levels of AnalysisT32NS007292 · NINDS · BRANDEIS UNIVERSITY · PI GINA G TURRIGIANO · 1986 to 2026
$12.7M
Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Activity-dependent regulation of membrane traffic and growth signaling in neuronsDP2NS082127 · NINDS · BRANDEIS UNIVERSITY · PI RODAL, AVITAL ADAH · 2012 to 2012
$2.4M
Investigating the generation of mechanical forces during tissue invaginationR01GM105984 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MARTIN, ADAM CHRISTOPHER · 2013 to 2021
$2.4M
NCCDPHP CDC HHS DP2 NS082127NIGMS NIH HHS R01 GM084947NIGMS NIH HHS R01-GM084947NIGMS NIH HHS R01 GM105984NINDS NIH HHS DP2 NS082127NINDS NIH HHS T32 NS007292
6 · The paper itself

Abstract

For the last 100 years, Drosophila melanogaster has been a powerhouse genetic system for understanding mechanisms of inheritance, development, and behavior in animals. In recent years, advances in imaging and genetic tools have led to Drosophila becoming one of the most effective systems for unlocking the subcellular functions of proteins (and particularly cytoskeletal proteins) in complex developmental settings. In this review, written for non-Drosophila experts, we will discuss critical technical advances that have enabled these cell biological insights, highlighting three examples of cytoskeletal discoveries that have arisen as a result: (1) regulation of Arp2/3 complex in myoblast fusion, (2) cooperation of the actin filament nucleators Spire and Cappuccino in establishment of oocyte polarity, and (3) coordination of supracellular myosin cables. These specific examples illustrate the unique power of Drosophila both to uncover new cytoskeletal structures and functions, and to place these discoveries in a broader in vivo context, providing insights that would have been impossible in a cell culture model or in vitro. Many of the cellular structures identified in Drosophila have clear counterparts in mammalian cells and tissues, and therefore elucidating cytoskeletal functions in Drosophila will be broadly applicable to other organisms.

Indexed as

ActinsActomyosinAnimalsCell PolarityCytoskeletal ProteinsCytoskeletonDrosophila melanogasterDrosophila ProteinsMicrofilament ProteinsModels, AnimalMyoblastsMyosinsOocytesOogenesisPhenotypeRNA, MessengerActinsActomyosinCytoskeletal ProteinsDrosophila ProteinsMicrofilament ProteinsMyosinsRNA, MessengeractinDrosophilamicrotubulemyoblastmyosinoocyte

Identifiers

PMID26074334
PMCPMC4782189

What OpenQuestion holds

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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.