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CRISPR-EVOL SIGNED

The eco-evolutionary costs and benefits of CRISPR-Cas systems, and their effect on genome diversity within populations

Total Cost €

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EC-Contrib. €

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Partnership

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 CRISPR-EVOL project word cloud

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

unessential    parasitic    environment    reduce    exchange    reveal    spacers    inter    opposite    plasmids    defense    immune    evolutionary    alter    full    infection    natural    acquisition    patterns    roles    population    species    cellular    eco    replicons    nature    strain    selfish    proteins    strains    memory    hypothesis    conversely    deletions    genetic    environmental    shown    chromosomes    unclear    benefits    mating    prokaryotes    assumed    cas    dna    induce    microbial    primarily    quantify    heritable    cells    contributes    unknown    viruses    additional    continual    crispr    indicating    lateral    explore    archaea    combined    experimental    shaping    viral    transfer    outweigh    generating    impede    generate    recombination    exact    regarding    avenues    incurred    scope    populations    evolution    suggest    supporting    genome    lineages    repair    events    absence    gene    immunity    diversity    acquired    diversification    reduces    acquire    genomics    involvement    genomic    anti    frequently    loci    genetics    again   

Project "CRISPR-EVOL" data sheet

The following table provides information about the project.

Coordinator
TEL AVIV UNIVERSITY 

Organization address
address: RAMAT AVIV
city: TEL AVIV
postcode: 69978
website: http://www.tau.ac.il/

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
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 Coordinator Country Israel [IL]
 Total cost 2˙495˙625 €
 EC max contribution 2˙495˙625 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-ADG
 Funding Scheme ERC-ADG
 Starting year 2018
 Duration (year-month-day) from 2018-05-01   to  2023-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    TEL AVIV UNIVERSITY IL (TEL AVIV) coordinator 2˙495˙625.00

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 Project objective

CRISPR-Cas systems are microbial defense systems that provide prokaryotes with acquired and heritable DNA-based immunity against selfish genetic elements, primarily viruses. However, the full scope of benefits that these systems can provide, as well as their costs remain unknown. Specifically, it is unclear whether the benefits against viral infection outweigh the continual costs incurred even in the absence of parasitic elements, and whether CRISPR-Cas systems affect microbial genome diversity in nature. Since CRISPR-Cas systems can impede lateral gene transfer, it is often assumed that they reduce genetic diversity. Conversely, our recent results suggest the exact opposite: that these systems generate a high level of genomic diversity within populations. We have recently combined genomics of environmental strains and experimental genetics to show that archaea frequently acquire CRISPR immune memory, known as spacers, from chromosomes of related species in the environment. The presence of these spacers reduces gene exchange between lineages, indicating that CRISPR-Cas contributes to diversification. We have also shown that such inter-species mating events induce the acquisition of spacers against a strain's own replicons, supporting a role for CRISPR-Cas systems in generating deletions in natural plasmids and unessential genomic loci, again increasing genome diversity within populations. Here we aim to test our hypothesis that CRISPR-Cas systems increase within-population diversity, and quantify their benefits to both cells and populations, using large-scale genomics and experimental evolution. We will explore how these systems alter the patterns of recombination within and between species, and explore the potential involvement of CRISPR-associated proteins in cellular DNA repair. This work will reveal the eco-evolutionary role of CRISPR-Cas systems in shaping microbial populations, and open new research avenues regarding additional roles beyond anti-viral defense

 Publications

year authors and title journal last update
List of publications.
2019 Israela Turgeman-Grott, Shirley Joseph, Sam Marton, Kim Eizenshtein, Adit Naor, Shannon M. Soucy, Aris-Edda Stachler, Yarden Shalev, Mor Zarkor, Leah Reshef, Neta Altman-Price, Anita Marchfelder, Uri Gophna
Pervasive acquisition of CRISPR memory driven by inter-species mating of archaea can limit gene transfer and influence speciation
published pages: 177-186, ISSN: 2058-5276, DOI: 10.1038/s41564-018-0302-8
Nature Microbiology 4/1 2020-01-28

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