The study of gene families in C. elegans by combinatioral RNA interference

Projektinformationen

COMBINATORIAL RNAI

ID Finanzhilfevereinbarung: 28870

Projekt abgeschlossen

Startdatum 30 Juni 2006

Enddatum 29 Juni 2007

Finanziert unter

• Human resources and Mobility in the specific programme for research, technological development and demonstration "Structuring the European Research Area" under the Sixth Framework Programme 2002-2006

Gesamtkosten € 0,00

EU-Beitrag € 40 000,00

Koordiniert durch

GHENT UNIVERSITY
Belgium

Ziel

Grazing ruminants are continuously exposed to nematode infection which, if uncontrolled, would restrict agricultural production. The most common of these nematodes are the cattle parasite Ostertagia ostertagi and the sheep parasites Haemonchus contortus an d Teladorsagia circumcincta. Control of infections is largely achieved using anthelmintics. However, farmers are facing an increasing problem with the appearance of resistant parasites. Vaccination is being considered as the most feasible alternative to an thelmintics. Useful levels of protection against these parasites have been achieved by vaccination with native worm antigens. Unfortunately it is unfeasible to harvest large quantities of these native antigens. The challenge is now to produce the antigens using DNA technology. However, biochemical analysis of the fractions have shown that they contain multiple members of nematode protein families, such as metallopeptidases, cysteine proteinases and activation associated secreted proteins. It is unclear whic h proteins of each family are necessary for the protection. It would be of great value to know the in vivo function of these proteins. It could indicate which ones are essential to the parasite and hence may be important for the protection. A powerful tool in this process may be the free living nematode Caenorhabditis elegans. This model organism is phylogenetically closely related to the parasites and its genome sequence is fully characterized. The primary focus of this project is to analyse the in vivo fu nction in C. elegans of the metallopeptidase, cysteine proteinase and activation associated secreted protein families and to identify the key genes in each family. This will be done by combinatorial RNAi, i.e. simultaneously interfering with the expression of multiple genes by RNAi. In a second step we will apply this technology to investigate the function of an additional nematode specific gene family, i.e. transthyretin-like protein family.

Wissenschaftliches Gebiet

• natural sciences › chemical sciences › inorganic chemistry › transition metals
• natural sciences › biological sciences › biochemistry › biomolecules › proteins
• medical and health sciences › basic medicine › pharmacology and pharmacy › pharmaceutical drugs › vaccines
• natural sciences › biological sciences › genetics › RNA
• agricultural sciences › animal and dairy science › domestic animals › animal husbandry

Programm/Programme

• FP6-MOBILITY - Human resources and Mobility in the specific programme for research, technological development and demonstration "Structuring the European Research Area" under the Sixth Framework Programme 2002-2006

Thema/Themen

• MOBILITY-4.1 - Marie Curie European Reintegration Grants (ERG)

Aufforderung zur Vorschlagseinreichung

FP6-2004-MOBILITY-11
Andere Projekte für diesen Aufruf anzeigen

Finanzierungsplan

ERG - Marie Curie actions-European Re-integration Grants

Koordinator

GHENT UNIVERSITY

• EU-Beitrag: Keine Daten
• Adresse: Sint-Pietersnieuwstraat 25 ; GENT ; Belgien
• Gesamtkosten: Keine Daten