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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.

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

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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