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TERMINATOR SIGNED

Ribosomal frameshifts as a novel mechanism to control RNA turnover in stress

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 TERMINATOR project word cloud

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

mechanisms    adaptability    preliminary    turnover    accumulated    manner    pool    abundance    interconnection    suggests    mediated    lab    ultimately    software    gene    stress    overcoming    community    human    cells    paramount    adapt    termination    ptcs    frameshifts    maintaining    tested    eliminates    existence    degradation    erroneous    cellular    mechanism    coupling    functional    explore    expression    serve    environment    dependent    window    suggesting    sense    maintenance    limiting    concentrations    surveillance    environmental    decay    fast    demonstrated    rna    technological    composition    host    mrna    nature    rf    premature    performing    nmd    regulated    fire    expand    induce    5pseq    talk    containing    transcripts    codons    datasets    ribosomal    signals    previously    nonsense    opens    transcription    yeast    aging    occurring    changing    homeostasis    telomere    regulation    cross    ptc    cell    regulates    translation    modulation   

Project "TERMINATOR" data sheet

The following table provides information about the project.

Coordinator
KAROLINSKA INSTITUTET 

Organization address
address: Nobels Vag 5
city: STOCKHOLM
postcode: 17177
website: www.ki.se

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 Sweden [SE]
 Total cost 191˙852 €
 EC max contribution 191˙852 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-08-01   to  2021-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KAROLINSKA INSTITUTET SE (STOCKHOLM) coordinator 191˙852.00

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 Project objective

Modulation of gene expression is key for maintaining cellular homeostasis in the changing environment. It is achieved through controlling the processes of transcription and RNA degradation that ultimately affect abundance and composition of the mRNA pool. Emerging evidence suggests that the pathways of RNA surveillance and degradation are of paramount importance for fast adaptation of gene expression to stress. One of the most studied mechanisms controlling RNA turnover is nonsense-mediated decay (NMD). It eliminates erroneous transcripts containing premature termination codons (PTC), and also regulates expression of functional transcripts in condition-dependent manner. Recently, my host lab has demonstrated existence of widespread coupling between mRNA decay and translation. This opens a new window for translation dependent regulation of RNA turnover. Specifically, recent studies show that ribosomal frameshifts (RF) occurring during translation induce PTCs and fire NMD response. Preliminary evidence from the host lab suggests that RF is regulated upon stress and could serve as a new mechanism to sense environmental signals and adapt mRNA concentrations. It is yet to be tested if such a regulation is of widespread nature in the cell. The main goal of this project is to investigate stress-dependent regulation of ribosomal frameshifts and their role in RNA turnover. The 5PSeq approach developed in the host lab will allow for performing high-scale analysis in yeast and human cells, and overcoming existing technological challenges previously limiting research in the field. This project will also explore the cross-talk between RNA turnover and telomere maintenance in cellular response to stress and aging. This will expand the accumulated evidence suggesting interconnection of RNA turnover with other processes involved in cellular adaptability. Finally, I will develop a software package for analysis of RNA degradation datasets that can be used by the research community.

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

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