Evidence map›Paper›PMID 25633995›Full record

ArticlePLoS genetics2015

A dPIP5K dependent pool of phosphatidylinositol 4,5 bisphosphate (PIP2) is required for G-protein coupled signal transduction in Drosophila photoreceptors.

Purbani Chakrabarti, Sourav Kolay, Shweta Yadav, Kamalesh Kumari, Amit Nair, Deepti Trivedi, Padinjat Raghu

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-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

24 citing papers in PubMed, 38 citations in OpenAlex.

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  9. Application of Fluorescent Proteins for Functional Dissection of theInternational journal of molecular sciences · 2021
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  14. A Genetic Screen inG3 (Bethesda, Md.) · 2020
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  15. Article
  16. Immunocytochemical Labeling of Rhabdomeric Proteins inThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2019
    Article
  17. Review
  18. 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

7 authors at 2 institutions in 2 countries.

Purbani ChakrabartiInositide Laboratory, Babraham Institute, Cambridge, United Kingdom.
Sourav KolayNational Centre for Biological Sciences, TIFR-GKVK Campus, Bangalore, India; Manipal University, Madhav Nagar, Manipal, Karnataka, India.
Shweta YadavNational Centre for Biological Sciences, TIFR-GKVK Campus, Bangalore, India.
Kamalesh KumariNational Centre for Biological Sciences, TIFR-GKVK Campus, Bangalore, India; Department of Biological Sciences, Tata Institute of Fundamental Research, Colaba, Mumbai, India.
Amit NairInositide Laboratory, Babraham Institute, Cambridge, United Kingdom.
Deepti TrivediInositide Laboratory, Babraham Institute, Cambridge, United Kingdom.
Padinjat RaghuInositide Laboratory, Babraham Institute, Cambridge, United Kingdom; National Centre for Biological Sciences, TIFR-GKVK Campus, Bangalore, India.
Babraham Institute · GBNational Centre for Biological Sciences · IN

Funding

Biotechnology and Biological Sciences Research CouncilDBT-Wellcome Trust India Alliance IA/S/14/2/501540
6 · The paper itself

Abstract

Multiple PIP2 dependent molecular processes including receptor activated phospholipase C activity occur at the neuronal plasma membranes, yet levels of this lipid at the plasma membrane are remarkably stable. Although the existence of unique pools of PIP2 supporting these events has been proposed, the mechanism by which they are generated is unclear. In Drosophila photoreceptors, the hydrolysis of PIP2 by G-protein coupled phospholipase C activity is essential for sensory transduction of photons. We identify dPIP5K as an enzyme essential for PIP2 re-synthesis in photoreceptors. Loss of dPIP5K causes profound defects in the electrical response to light and light-induced PIP2 dynamics at the photoreceptor membrane. Overexpression of dPIP5K was able to accelerate the rate of PIP2 synthesis following light induced PIP2 depletion. Other PIP2 dependent processes such as endocytosis and cytoskeletal function were unaffected in photoreceptors lacking dPIP5K function. These results provide evidence for the existence of a unique dPIP5K dependent pool of PIP2 required for normal Drosophila phototransduction. Our results define the existence of multiple pools of PIP2 in photoreceptors generated by distinct lipid kinases and supporting specific molecular processes at neuronal membranes.

Indexed as

AnimalsCell MembraneCytoskeletonDrosophilaDrosophila melanogasterLight Signal TransductionMembrane ProteinsOcular Physiological PhenomenaPhosphatidylinositol 4,5-DiphosphatePhosphoinositide Phospholipase CPhosphotransferases (Alcohol Group Acceptor)Photoreceptor CellsRetinaSignal Transduction1-phosphatidylinositol-4-phosphate 5-kinaseMembrane ProteinsPhosphatidylinositol 4,5-DiphosphatePhosphoinositide Phospholipase CPhosphotransferases (Alcohol Group Acceptor)

Identifiers

PMID25633995
PMCPMC4310717
OpenAlexW2048117837

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.