Explore the words cloud of the LARP4MOT project. It provides you a very rough idea of what is the project "LARP4MOT" about.
The following table provides information about the project.
Coordinator |
KING'S COLLEGE LONDON
Organization address contact info |
Coordinator Country | United Kingdom [UK] |
Project website | https://www.kcl.ac.uk/lsm/research/divisions/randall/research/sections/structural/conte/index.aspx |
Total cost | 183˙454 € |
EC max contribution | 183˙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-2014 |
Funding Scheme | MSCA-IF-EF-ST |
Starting year | 2016 |
Duration (year-month-day) | from 2016-09-01 to 2018-08-31 |
Take a look of project's partnership.
# | ||||
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1 | KING'S COLLEGE LONDON | UK (LONDON) | coordinator | 183˙454.00 |
RNA-binding proteins (RBPs) act at multiple levels to regulate gene expression, including mRNA splicing, polyadenylation, localisation, stability, decay and translational efficiency and, although central to health and disease, much of this precise concerted regulation remains to be uncovered. The recently discovered LARP4 is an RBP that affects mRNA stability and binds to polyA as well as the polyA-binding protein (PABP). Intriguingly, LARP4 has recently been identified as a regulator of cell morphology and migration in an RNAi screen, but little is known about how control of gene expression at the translational level is coordinated during cell migration and invasion. Since aberrant cell migration contributes to the development of human diseases including cancer, chronic inflammation and atherosclerosis, LARP4 represents an excellent RBP to advance our understanding of key cellular mechanisms relating to mRNA processing and turnover. The overall aim of the project is to understand at a molecular level how LARP4 regulates mRNA translation and how this impacts on cell migration, especially in the context of cancer cell biology, using human prostate cancer cell lines as models. For this, a multidisciplinary approach combining biochemistry, biophysics, structural and cell biology will be used.
year | authors and title | journal | last update |
---|---|---|---|
2017 |
Richard J. Maraia, Sandy Mattijssen, Isabel Cruz-Gallardo, Maria R. Conte The La and related RNA-binding proteins (LARPs): structures, functions, and evolving perspectives published pages: e1430, ISSN: 1757-7004, DOI: 10.1002/wrna.1430 |
Wiley Interdisciplinary Reviews: RNA 8/6 | 2019-04-18 |
2019 |
Isabel Cruz-Gallardo, Luigi Martino, Roberta Trotta, Stefano De Tito, Geoff Kelly, R. Andrew Atkinson, Antonio Randazzo, Maria R. Conte Resonance assignment of human LARP4A La module published pages: , ISSN: 1874-2718, DOI: 10.1007/s12104-019-09871-4 |
Biomolecular NMR Assignments | 2019-02-27 |
2019 |
Isabel Cruz-Gallardo, Luigi Martino, Geoff Kelly, R Andrew Atkinson, Roberta Trotta, Stefano De Tito, Pierre Coleman, Zainab Ahdash, Yifei Gu, Tam T T Bui, Maria R Conte LARP4A recognizes polyA RNA via a novel binding mechanism mediated by disordered regions and involving the PAM2w motif, revealing interplay between PABP, LARP4A and mRNA published pages: 4272-4291, ISSN: 0305-1048, DOI: 10.1093/nar/gkz144 |
Nucleic Acids Research 47/8 | 2019-09-13 |
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The information about "LARP4MOT" are provided by the European Opendata Portal: CORDIS opendata.
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