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WISDOM SIGNED

The autonomous floral pathway: a WIndow to Study the tight link between non-coDing RNA and chrOMatin regulation

Total Cost €

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EC-Contrib. €

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Partnership

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 WISDOM project word cloud

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

contact    host    myself    building    regulate    competences    biochemistry    rna    antisense    gained    base    interconnections    coolair    molecular    h3k4    alternative    training    unknown    generally    academic    nature    transferable    reproductive    international    drive    chromatin    eukaryotes    histone    delivers    triggered    transcription    interconnection    goals    missing    protein    conserved    transcript    strategy    floral    fld    collaborative    repression    capitalize    demethylase    substantial    plays    expression    identification    mediated    controls    plant    action    genetics    sdg26    coding    hypothesis    career    mechanism    components    locus    genome    histones    experimental    central    mobility    proteomic    silencing    skills    arabidopsis    methylate    mechanistic    me    lab    creative    my    output    co    deeper    proximal    explore    fy    specificity    elusive    engagement    fca    biology    stable    proteins    sense    networks    fellowship    represses    environment    suggests    public    skillset    flc    splicing    repressor    contributes    link    transcriptional    regulation    polyadenylation    domain    quantitative   

Project "WISDOM" data sheet

The following table provides information about the project.

Coordinator
JOHN INNES CENTRE 

Organization address
address: NORWICH RESEARCH PARK COLNEY
city: NORWICH
postcode: NR4 7UH
website: www.jic.bbsrc.ac.uk

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 United Kingdom [UK]
 Total cost 195˙454 €
 EC max contribution 195˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-04-01   to  2020-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    JOHN INNES CENTRE UK (NORWICH) coordinator 195˙454.00

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 Project objective

My Fellowship will explore the interconnection between non-coding RNA and chromatin regulation. Building on a detailed mechanistic base, I will capitalize on the recent proteomic identification of a stable complex FLD/SDG26 by my host lab, which plays a central role in the co-transcriptional silencing of the Arabidopsis floral repressor locus FLC. This protein complex is central to a mechanism determining the quantitative expression level of FLC, and thus the reproductive strategy of the plant. However, these activities also regulate many other targets in the Arabidopsis genome and the conserved nature of the components suggests the deeper understanding gained from this study will be important generally across all eukaryotes. FLD is a histone demethylase with specificity for H3K4; SDG26 is a SET domain protein likely to methylate histones and other proteins, but whose specificity is currently unknown. The splicing and alternative processing of FLC antisense non-coding transcript, COOLAIR, is essential for the repression of FLC transcription. However, how the processing of COOLAIR controls sense transcription remains elusive. My proposal aims to: 1) test the hypothesis that the FLD/SDG26 complex, triggered by FCA/FY-mediated proximal polyadenylation of COOLAIR, delivers a specific chromatin environment, which represses transcriptional output: and 2) explore the missing link between FCA/FY-mediated proximal polyadenylation of COOLAIR and chromatin regulation by FLD/SDG26 complex. My proposal involves interconnections between genetics, biochemistry and molecular biology, enabling me to develop a broader experimental skillset. It directly contributes to the action’s goals to: improve my creative potential and competences through international mobility and advanced training in technical and transferable skills; enhance collaborative and contact networks for both myself and my host lab through academic and public engagement; and drive substantial career development.

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