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Forschungsstelle
EU FRP
Projektnummer
03.0165-1
Projekttitel
GENINTEG: Controlled gene integration: a requisite for genome analysis and gene therapy
Projekttitel Englisch
GENINTEG: Controlled gene integration: a requisite for genome analysis and gene therapy

Texte zu diesem Projekt

 DeutschFranzösischItalienischEnglisch
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Forschungsprogramme
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Kurzbeschreibung
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Abstract
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Erfasste Texte


KategorieText
Schlüsselwörter
(Englisch)
Molecular genetics; Genomics; applied biology

Alternative Projektnummern
(Englisch)
EU project number: 503303
Forschungsprogramme
(Englisch)
EU-programme: 6. Frame Research Programme - 1.1.1a
Kurzbeschreibung
(Englisch)
See abstract
Abstract
(Englisch)
Despite the enormous potential of using transgenesis for gene function analysis and gene therapy, little is known about the mechanism of gene integration in eukaryotic cells. Transgene integration into the chromosomes of living cells can occur either randomly or targeted by homologous recombination. The later type of integration is the most powerful, because it allows to precisely delete or modify sequences at defined chromosomal positions.
A consortium is formed to study gene integration by recombination in a number of different model organisms. As DNA repair is conserved during evolution, a comparative genomics approach is proposed to discover evolutionary conserved principles of gene integration. An explicit goal is to understand why targeted integration occurs efficiently in some eukaryotic cells, but not in others. One explanation to be investigated is that the ratios of targeted to random integration reflects to the balance between DNA double-strand break repair by homologous recombination and end-joining. Other areas of research will relate to site-specific integration by adeno-associated viruses, T-DNA elements and serine recombinases.
The insight into the mechanism of gene integration will be used to increase the efficiency of targeted gene integration in cells, where targeted integration events are currently hard to detect. This might be achieved either by modification of the gene constructs or their transfer into the cell nucleus or by regulating the expression of transacting recombination factors. As gene targeting is the only way to precisely modify the genetic blueprint of living cells in vivo, improvements of this technique offer immense opportunities not only for basic research, but also for biotechnology and gene therapy. This ranges from fine-tuning protein production in plants and bio-reactors to gene therapy for autosomal dominant defects. A SME is included in the proposal to capture these opportunities and reinforce the competitiveness.
Datenbankreferenzen
(Englisch)
Swiss Database: Euro-DB of the
State Secretariat for Education and Research
Hallwylstrasse 4
CH-3003 Berne, Switzerland
Tel. +41 31 322 74 82
Swiss Project-Number: 03.0165-1