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CHERI

Chromatin targeting and remodelling by bacterial effectors in plant immunity

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 CHERI project word cloud

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

nuclear    immunity    virulence    interferes    elucidate    perturbations    modulated    structurally    machinery    bacterial    receptor    underlying    probes    rely    pathogens    actions    signalling    challenged    converted    hypothesize    viruses    effectors    unrelated    genes    host    receptors    instead    intracellular    health    proteins    plants    functional    interact    unlike    fundamental    intercepted    triggered    found    environment    bacteria    senses    immune    successful    infection    causing    suppress    suggest    molecular    sites    heteromeric    agriculture    nature    sustainable    activation    mechanisms    transduced    resistance    encoding    converge    innate    chromatin    mammals    forms    signals    systemic    perceive    capacity    connected    remodelling    circulating    lack    effector    defence    disease    pair    recognition    components    domains    arabidopsis    disseminate    cell    pathogen    basal    mount    plant    physically    certain    human    modifications    histone    fungi    unclear    overlapping   

Project "CHERI" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: MUENCHEN
postcode: 80539
website: n.a.

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]
 Project website http://www.mpipz.mpg.de/parker
 Total cost 159˙460 €
 EC max contribution 159˙460 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2016
 Duration (year-month-day) from 2016-04-01   to  2018-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (MUENCHEN) coordinator 159˙460.00

Map

 Project objective

In nature, plants are challenged by disease-causing pathogens such as viruses, bacteria and fungi. Understanding mechanisms of plant disease and disease resistance is of fundamental importance to sustainable agriculture and human health. Unlike mammals, plants lack a circulating immune system. Plants instead rely on the innate immune capacity of each cell and systemic signals that disseminate from infection sites. Successful pathogens use effectors to suppress plant immunity and cause disease. Plants have evolved disease resistance genes encoding immune receptors that perceive specific pathogen effectors to mount effector-triggered immunity. In Arabidopsis, a heteromeric pair of intracellular immune receptors forms a functional recognition complex which senses virulence activities of two structurally unrelated bacterial effectors at the nuclear chromatin. Results suggest that effector targeting of histone modifications and chromatin remodelling interferes with host basal immunity and that this is transduced by the receptor pair to activation of defence pathways. The underlying molecular mechanisms remain unclear. We have found that the two bacterial effectors interact with an overlapping set of chromatin-associated proteins and with certain immune receptor domains. We hypothesize that the effectors converge on the same chromatin machinery for promoting disease and that their actions are intercepted by the immune receptor system which is physically connected to basal immunity signalling components. By using the effectors as molecular probes, this proposal aims to elucidate how the chromatin environment is modulated during infection and how effector perturbations are converted to effective immunity.

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The information about "CHERI" are provided by the European Opendata Portal: CORDIS opendata.

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