Difference between revisions of "Team:Valencia UPV"

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                    <p id="absp">Covering food necessities is mandatory, but
 
                    resources are not sustainably exploited. Global strategies
 
                    to increase food productivity and quality need to be
 
                    concealed with a local perspective, providing breeders with
 
                    the necessary technology to improve varieties. The aim of
 
                    HYPE-IT is to decrease current technological barriers for
 
                    breeding local crops using precision genome engineering,
 
                    easing the gene editing process using SynBio-inspired
 
                    simplified CRISPR/Cas9 tools. HYPE-IT brings along a
 
                    software tool that associates crop traits with specific
 
                    gene targets and designs optimal gRNAs for those targets.
 
                    HYPE-IT also incorporates a modular gene circuit that
 
                    serves as an in vivo gRNA testing system, ensuring
 
                    appropriate gRNA choice even when no precise sequence
 
                    information of local varieties is available. We aim to
 
                    develop a split-Cas9 system based on viral vectors to
 
                    efficiently deliver the editing machinery into the plant,
 
                    and to create an affordable Labcase with the necessary
 
                    laboratory equipment for HYPE-IT.</p>
 
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                                <h2 class="expand_title">Data Processing
 
                                Software</h2>
 
                                <p class="expandp">We have created a genomic
 
                                data processing software. This tool allows the
 
                                user to choose the type of plant and phenotypic
 
                                variation of interest. The software will find
 
                                the gene associated with that phenotype, and
 
                                then it will give as output the optimal guide
 
                                RNA that will be used with Cas9 for knock-out
 
                                the gene. Open source will be the main
 
                                philosophy of this software, so anyone can
 
                                contribute with new parameters or new
 
                                phenotype-gene links.</p>
 
                                <a class="btn btn-default btn_home" href="#" role="button">Link</a>
 
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                            <h2 class="expand_title">gRNA Testing System</h2>
 
                            <p>The plant breeder could test the obtained guide
 
                            RNA directly in his plant, but it would take a long
 
                            time just to check if it works or not. To avoid
 
                            this, we have designed a gRNA Testing System which
 
                            does this in a fast and simple way. Using Nicotiana
 
                            benthamiana, Agrobacterium infection system, a
 
                            short sequence of the gene of his plant and a
 
                            luciferase assay, the users will surely know if the
 
                            guide RNA works on his own variety. This system
 
                            works as a switch that will show luciferase if the
 
                            gene has been knocked-out.</p>
 
                            <a class="btn btn-default btn_home" href="#" role="button">Read More</a>
 
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                            <h2 class="expand_title">Split Cas9</h2>
 
                            <p>As a vehicle to genetically modify the plant,
 
                            the Agrobacterium infection system is inefficient,
 
                            long and difficult. Thus, we decide to use a viral
 
                            system to enhance plant infection. Since the viral
 
                            vectors are small, the Cas9 and CPF1 endonuclease -
 
                            necessary for editing - need to be splitted in two
 
                            parts. To reassemble them inside the plant cells,
 
                            we will use intein proteins.</p>
 
                            <a class="btn btn-default btn_home" href="#" role="button">Read More</a>
 
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                            <h2 class="expand_title">Lab-Case</h2>
 
                            <p>We want to make plant gene editing accessible
 
                            for all potential users, even if they do not have
 
                            an advanced laboratory. To achieve this goal, we
 
                            have made a Lab-case, a hardware set up which
 
                            contains all the laboratory equipment and the
 
                            necessary reagents required to perform genome
 
                            editing, with simple protocols. This guarantees
 
                            availability for agricultural cooperatives,
 
                            start-ups, garage laboratories... This will be the
 
                            future of agriculture: making genome editing of
 
                            plants accessible to everyone.</p>
 
                            <a class="btn btn-default btn_home" href="#" role="button">Read More</a>
 
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Revision as of 14:45, 2 September 2016