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CYCLODE SIGNED

Cyclical and Linear Timing Modes in Development

Total Cost €

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EC-Contrib. €

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Partnership

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 CYCLODE project word cloud

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

genomic    genetic    screens    times    segmentation    signal    regenerative    ratio    worms    combination    genes    gain    additionally    imaging    individual    fate    coupling    medicine    apparent    stem    fundamental    microchamber    developmental    cells    tracking    clock    regulatory    biological    fates    events    advancing    timer    timers    clocks    mechanisms    nematode    manipulations    stage    poorly    live    tools    coordinated    discovery    20    linear    choices    roundworm    vivo    cell    prototypic    elucidate    gene    foresee    employing    organismal    mrna    perturbations    architecture    patterning    temporal    molting    elegans    heterochronic    timing    proper    wiring    resolution    little    food    recurring    cyclic    computational    reveal    nearly    global    understand    worm    goals    oscillates    cyclical    appropriate    rhythmic    larval    oscillations    vertebrate    components    gained    unknown    transcriptome    manifestation    noise    animal    sequencing    deprivation    expression   

Project "CYCLODE" data sheet

The following table provides information about the project.

Coordinator
FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION 

Organization address
address: MAULBEERSTRASSE 66
city: BASEL
postcode: 4058
website: www.fmi.ch

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 Switzerland [CH]
 Total cost 2˙358˙625 €
 EC max contribution 2˙358˙625 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-ADG
 Funding Scheme ERC-ADG
 Starting year 2017
 Duration (year-month-day) from 2017-10-01   to  2022-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION CH (BASEL) coordinator 2˙358˙625.00

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 Project objective

Organismal development requires proper timing of events such as cell fate choices, but the mechanisms that control temporal patterning remain poorly understood. In particular, we know little of the cyclical timers, or ‘clocks’, that control recurring events such as vertebrate segmentation or nematode molting. Furthermore, it is unknown how cyclical timers are coordinated with the global, or linear, timing of development, e.g. to ensure an appropriate number of cyclical repeats. We propose to elucidate the components, wiring, and properties of a prototypic developmental clock by studying developmental timing in the roundworm C. elegans. We build on our recent discovery that nearly 20% of the worm’s transcriptome oscillates during larval development – an apparent manifestation of a clock that times the various recurring events that encompass each larval stage. Our aims are i) to identify components of this clock using genetic screens, ii) to gain insight into the system’s architecture and properties by employing specific perturbations such as food deprivation, and iii) to understand the coupling of this cyclic clock to the linear heterochronic timer through genetic manipulations. To achieve our ambitious goals, we will develop tools for mRNA sequencing of individual worms and for their developmental tracking and microchamber-based imaging. These important advances will increase temporal resolution, enhance signal-to-noise ratio, and achieve live tracking of oscillations in vivo. Our combination of genetic, genomic, imaging, and computational approaches will provide a detailed understanding of this clock, and biological timing mechanisms in general. As heterochronic genes and rhythmic gene expression are also important for controlling stem cell fates, we foresee that the results gained will additionally reveal regulatory mechanisms of stem cells, thus advancing our fundamental understanding of animal development and future applications in regenerative medicine.


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