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SOLID SIGNED

Suppression of Organelle Defects in Human Disease

Total Cost €

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EC-Contrib. €

0

Partnership

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 SOLID project word cloud

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

mutations    genes    engineering    perturbed    possibilities    fixed    fitness    initial    environmental    etiological    groundbreaking    reveal    entirely    exemplified    systematic    revealing    defects    combines    yielding    suppressors    time    malfunctioning    questions    mitochondria    function    first    view    create    extensive    mutants    perturbation    alter    cures    impaired    remove    incurable    interrogate    instead    eukaryotic    disease    relies    metabolic    hundreds    amount    independent    cellular    hidden    mapping    correct    mostly    suppression    organisms    mutation    fashion    therapeutic    alongside    human    hurdles    urgently    stratification    organelles    difficulty    paradigm    substantial    frustrations    captures    genetics    disorders    query    triggers    limited    yeast    departs    mainly    applicable    machines    point    contain    solid    modules    diversity    absent    biological    ultradeep    organelle    lysosomes    fidelity    concerted    altogether    uniquely    haploid    mutagenesis    strategies    cell    causative    functioning    direct    neurodegeneration    drugging    genetic    platform    model    exhaustive    surveys    phenotypes    biology    suppressor    genome    until    centric    diseases    uncover    recessive    gene    lacking   

Project "SOLID" data sheet

The following table provides information about the project.

Coordinator
LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN 

Organization address
address: GESCHWISTER SCHOLL PLATZ 1
city: MUENCHEN
postcode: 80539
website: www.uni-muenchen.de

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 Germany [DE]
 Total cost 1˙498˙400 €
 EC max contribution 1˙498˙400 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-07-01   to  2024-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN DE (MUENCHEN) coordinator 1˙498˙400.00

Map

 Project objective

The goal of SOLID is the systematic mapping of genetic suppression for important organelles with impaired fidelity in human disease to uncover new strategies to correct the perturbed state. Functioning of the eukaryotic cell relies on the concerted activity of biological machines, defects in which can cause incurable human disease, including metabolic disorders and neurodegeneration. This is exemplified by malfunctioning mitochondria or lysosomes, for which (alongside environmental triggers) hundreds of causative genes have been identified, but cures are mostly lacking. This is mainly due to the difficulty of drugging loss-of-function mutations, which uniquely alter or entirely remove the gene product. Extensive studies in yeast and initial work in the human system show that cellular modules contain a substantial amount of hidden genetic suppression. Revealing suppressors of disease-defining features of organelle perturbation and targeting those instead of the query mutations, will address the frustrations of drugging an absent factor and etiological diversity. Until now, mutation-based genome-wide suppressor surveys were mostly limited to model organisms and phenotypes yielding growth defects, due to technical hurdles associated with recessive genetics in the human system. However, with the development of a groundbreaking new forward genetics platform that combines genome engineering, ultradeep haploid mutagenesis and direct stratification of fixed mutants, we can now, for the first time, interrogate genetic suppression of human organelle defects independent of cellular fitness. SOLID will also develop new technology to study organelle fidelity in an exhaustive fashion that departs from a gene-centric view point and captures complex phenotypes. Altogether, this will create a new paradigm of 'studying cell biology via genetics' widely applicable to many different biological questions, and reveal urgently needed novel therapeutic possibilities for incurable diseases.

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The information about "SOLID" are provided by the European Opendata Portal: CORDIS opendata.

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