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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.

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

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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