Evidence map›Paper›PMID 20574526›Full record

ArticlePloS one2010

The Drosophila GIPC homologue can modulate myosin based processes and planar cell polarity but is not essential for development.

Alexandre Djiane, Marek Mlodzik

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  5. Article
  6. Review
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  8. Function and cancer genomics of FAT family genes (review).International journal of oncology · 2012
    Review
  9. Article
  10. Article
  11. Article
  12. Proteomics approach to study the functions of Drosophila myosin VI through identification of multiple cargo-binding proteins.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  13. 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 2 institutions in 2 countries.

Alexandre DjianeDepartment of Physiology Development and Neuroscience, University of Cambridge, Cambridge, UK.
Marek Mlodzik
Icahn School of Medicine at Mount Sinai · USUniversity of Cambridge · GB

Funding

Establishment of Epithelial Planar Cell PolarityR01GM062917 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI MLODZIK, MAREK · 2001 to 2013
$4.6M
NIGMS NIH HHS R01 GM062917NIGMS NIH HHS R01 GM62917
6 · The paper itself

Abstract

Epithelia often show, in addition to the ubiquitous apico-basal (A/B) axis, a polarization within the plane of the epithelium, perpendicular to the A/B axis. Such planar cell polarity (PCP) is for example evident in the regular arrangement of the stereocilia in the cochlea of the mammalian inner ear or in (almost) all Drosophila adult external structures. GIPCs (GAIP interacting protein, C terminus) were first identified in mammals and bind to the Galphai GTPase activating protein RGS-GAIP. They have been proposed to act in a G-protein coupled complex controlling vesicular trafficking. Although GIPCs have been found to bind to numerous proteins including Frizzled receptors, which participate in PCP establishment, there is little in vivo evidence for the functional role(s) of GIPCs. We show here that overexpressed Drosophila dGIPC alters PCP generation in the wing. We were however unable to find any binding between dGIPC and the Drosophila receptors Fz1 and Fz2. The effect of overexpressed dGIPC is likely due to an effect on the actin cytoskeleton via myosins, since it is almost entirely suppressed by removing a genomic copy of the Myosin VI/jaguar gene. Surprisingly, although dGIPC can interfere with PCP generation and myosin based processes, the complete loss-of-function of dGIPC gives viable adults with no PCP or other detectable defects arguing for a non-essential role of dGIPC in viability and normal Drosophila development.

Indexed as

Cell PolaritySequence Homology, Amino AcidActinsAnimalsCarrier ProteinsCytoskeletonDrosophila melanogasterDrosophila ProteinsFemaleGene Expression RegulationMaleMembrane ProteinsMyosin Heavy ChainsMyosinsSequence DeletionWings, AnimalActinsCarrier ProteinsDrosophila Proteinskermit protein, DrosophilaMembrane ProteinsMyosin Heavy ChainsMyosinsmyosin VIZip protein, Drosophila

Identifiers

PMID20574526
PMCPMC2888583
OpenAlexW2046847450

What OpenQuestion holds

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LicenceCC BY
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.