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Content archived on 2024-06-16

Sequence specific Oligomers for in vivo DNA repair

Objective

Sequence-specific alteration of genes in living organisms using small oligomers, as has been recently successfully demonstrated by us, could provide a new strategy for targeted gene repair or trait alteration. The applying consortium has in the last years developed a concept of using small dual oligomers to introduce in vivo site-targeted specific sequence alterations, and has advanced the toolkit for synthesis and functional testing of these oligomers using biophysical, biochemical and molecular biology methods.

The oligomers (ROs) are composed of two functional domains: a targeting domain that provides high sequence affinity to any desired location in the genome, and a template domain that activates the cellular repair machinery by active group-transfer to induce small sequence changes without leaving foreign sequences. Hitherto the consortium has reached its goal of the 5th framework defined as in vivo rates of targeted sequence correction over 2% on a standardised cellular readout.

The goal of the suggest ed work in the 6th framework is to further improve the design of platform technology to induce precise single-base changes in a cell culture readout at rates between 2 and 5% and in a selected disease locus without collateral damage. ROs provide a new paradigm for in vivo genetic engineering and a novel tool to be tested for its use in somatic gene therapy.

Fields of science (EuroSciVoc)

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Keywords

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Topic(s)

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Call for proposal

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FP6-2003-LIFESCIHEALTH-I
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Funding Scheme

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STREP - Specific Targeted Research Project

Coordinator

RIKSHOSPITALET
EU contribution
No data
Address
Sognsvannsveien 20
OSLO
Norway

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Total cost

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Participants (11)

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