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SOLID SIGNED

Suppression of Organelle Defects in Human Disease

Total Cost €

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EC-Contrib. €

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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.

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

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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