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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.

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

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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