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FLYghtCaRe

Ca2+ feedback control of TRP/TRPL channels in Drosophila photoreceptors

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EC-Contrib. €

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Partnership

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 FLYghtCaRe project word cloud

Explore the words cloud of the FLYghtCaRe project. It provides you a very rough idea of what is the project "FLYghtCaRe" about.

feedback    light    obtain    electrophysiology    illumination    transient    fly    explore    generating    enriching    mechanisms    resolution    regulatory    made    starlit    calmodulin    fruitfly    entry    will    characterise    flies    interaction    contrast    genetically    laboratory    full    virtually    encoded    phototransductive    physiological    ciliary    channels    trpl    chimeric    negative    mutated    sun    dynamics    dramatic    class    modulates    optogenetics    compartments    themselves    photons    trp    core    ca2    responsible    signalling    cascade    phenotypes    displaying    first    detect    phototransduction    difference    binding    performance    termination    responding    vertebrates    spatial    indicators    visual    night    cellular    combine    positive    reliably    rhabdomeric    dark    precise    cell    retinal    sophistication    hypotheses    ambient    world    midday    unknown    subcellular    rising    skills    intact    compound    receptor    single    activated    rods    dissecting    defective    optics    imaged    daylight    amplification    continue    professional    photoreceptors    loops    mutants    bump    gain    sites    molecular    bumps    expressing    degeneration    eye    lie    quantum   

Project "FLYghtCaRe" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Project website https://www.pdn.cam.ac.uk/directory/asteriti
 Total cost 183˙454 €
 EC max contribution 183˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-11-01   to  2017-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 183˙454.00

Map

 Project objective

A major challenge for any visual system is the dramatic difference in ambient light between a starlit night and midday sun. In contrast to the ciliary rods of vertebrates, the rhabdomeric photoreceptors of the common fruitfly not only reliably detect single photons when dark-adapted (generating responses called ‘quantum bumps’), but continue responding in full daylight. At the core of this performance lie positive and negative feedback loops, many involving Ca2 entry through the light activated transient receptor potential channels TRP and TRPL. Although Ca2 modulates virtually every step of the phototransductive cascade, key targets are the channels themselves, leading to: (i) amplification by positive feedback during the rising phase of quantum bumps, (ii) gain reduction by negative feedback during quantum bump termination and during light adaptation. Our objectives are to combine single cell electrophysiology and optogenetics to explore Ca2 signalling in fly photoreceptors, dissecting both its molecular interaction with TRP and TRPL channels and its dynamics within the cell. Our first aim will be to characterise the role of Calmodulin binding sites and other unknown regulatory sites on TRP and TRPL, in the feedback loops described above. Flies expressing mutated and chimeric TRP/TRPL channels will be used. Our second aim will be to obtain measurements of Ca2 dynamics with subcellular spatial resolution under physiological illumination. Genetically encoded Ca2 indicators will be targeted to specific cellular compartments and imaged in intact flies by exploiting the optics of the compound eye. Measurements will be made in fly mutants displaying defective light responses and retinal degeneration, leading to precise hypotheses on the mechanisms responsible for their phenotypes. This project will bring our understanding of rhabdomeric phototransduction to a new level of sophistication, while enriching my professional skills in a world-class laboratory.

 Publications

year authors and title journal last update
List of publications.
2017 Sabrina Asteriti, Che-Hsiung Liu, Roger C. Hardie
Calcium signalling in Drosophila photoreceptors measured with GCaMP6f
published pages: , ISSN: 0143-4160, DOI: 10.1016/j.ceca.2017.02.006
Cell Calcium 2019-06-14

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