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出 处:《Molecular Plant》2015年第8期1292-1294,共3页分子植物(英文版)
摘 要:Dear Editor The use of sequence-specific nucleases for plant genomic DNA mutagenesis is an exciting and rapidly developing tech- nology (Voytas and Merchant, 2013; Baltes and Voytas, 2014). To date, most mutated plants have been recovered from transgenic plants stably expressing nucleases. However, transient nuclease delivery by plant DNA- and RNA-based viral vectors followed by regeneration of plantlets from modi- fied tissues has emerged as an alternative, efficient strategy in some plant species (Marton et al., 2010; Baltes et al., 2014). Delivery of nucleases by plant RNA viruses is particularly attractive because they typically do not integrate into the plant genome, and therefore the mutated plants are not classified as transgenic (Marton et al., 2013; Voytas and Gao, 2014).Dear Editor The use of sequence-specific nucleases for plant genomic DNA mutagenesis is an exciting and rapidly developing tech- nology (Voytas and Merchant, 2013; Baltes and Voytas, 2014). To date, most mutated plants have been recovered from transgenic plants stably expressing nucleases. However, transient nuclease delivery by plant DNA- and RNA-based viral vectors followed by regeneration of plantlets from modi- fied tissues has emerged as an alternative, efficient strategy in some plant species (Marton et al., 2010; Baltes et al., 2014). Delivery of nucleases by plant RNA viruses is particularly attractive because they typically do not integrate into the plant genome, and therefore the mutated plants are not classified as transgenic (Marton et al., 2013; Voytas and Gao, 2014).
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