Opendata, web and dolomites

CRISPR-Locate SIGNED

Linking sequence to function of long noncoding RNAs with CRISPR.

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 CRISPR-Locate project word cloud

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

pressing    created    experimentally    significance    molecule    throughput    noncoding    modular    discoveries    faster    conventional    biological       surprise    mature    experiments    lncrna    natural    medicine    genes    19    delete    endogenous    resource    closer    linking    human    primary    technique    insert    mutated    1000    crispr    subsequently    separable    handful    detecting    annotation    context    sequence    localization    create    protein    laborious    molecules    push    genome    afterwards    tagged    lncrnas    contains    fractionate    wake    function    characterised    hypothesis    rna    place    encode    grand    cells    rnas    coding    locate    vast    time    10    lt    discovery    encoded    invaluable    estimates    alongside    domains    simultaneously    efforts    tags    elucidated    extensive    deletion    discovering    presently       biology    wild    subcellular    least    functions    proxy    map    responsible    proteins    localisation    unlocking    compartments    question    functional    purify   

Project "CRISPR-Locate" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAET BERN 

Organization address
address: HOCHSCHULSTRASSE 6
city: BERN
postcode: 3012
website: http://www.unibe.ch

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 Switzerland [CH]
 Total cost 191˙149 €
 EC max contribution 191˙149 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2019
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2021
 Duration (year-month-day) from 2021-07-01   to  2023-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAET BERN CH (BERN) coordinator 191˙149.00

Map

 Project objective

A great surprise in the wake of the Human Genome Project has been the discovery of vast numbers of RNAs that do not encode proteins. Alongside 19,000 protein-coding genes, our genome contains at least 20,000 long noncoding RNA (lncRNA) genes, but recent estimates push that number to 100,000. Extensive annotation efforts are presently discovering lncRNAs far faster than their functions can be elucidated, and thus only <1% of lncRNAs have been experimentally characterised. These discoveries have created a grand challenge of understanding lncRNAs’ biological significance. To do this, we must solve the pressing question of how lncRNAs’ functions are encoded in their primary sequence. As a proxy of lncRNAs function we can use subcellular localisation since lncRNAs function as a mature RNA molecule. One hypothesis is that, similar to proteins, lncRNAs are modular molecules composed of separable functional domains. Previous studies, including my own, have used conventional methods to identify domains in a handful of lncRNAs by laborious deletion experiments. I propose to advance this field, via a novel high-throughput technique, CRISPR-Locate, capable of detecting lncRNA domains and their function in their natural endogenous context. I will delete ⁓1000 different lncRNA domains at the same time and simultaneously insert RNA tags at their place. Subsequently, I will fractionate cells by their compartments and purify tagged lncRNAs. Afterwards, I will sequence all the tagged lncRNAs and, by comparing the change in the subcellular localisation between mutated and wild type cells, I will identify which domains are responsible for subcellular localization. Finally, I will use CRISPR-Locate to create a map of lncRNA domains, an invaluable resource linking sequence to function, and bring us a step closer to unlocking the potential of 10^4 novel genes in medicine and biology.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "CRISPR-LOCATE" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "CRISPR-LOCATE" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

LiverMacRegenCircuit (2020)

Elucidating the role of macrophages in liver regeneration and tissue unit formation

Read More  

CYBERSECURITY (2018)

Cyber Security Behaviours

Read More  

HSQG (2020)

Higher Spin Quantum Gravity: Lagrangian Formulations for Higher Spin Gravity and Their Applications

Read More