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Efficient scar-free knock-ins of several kilobases in plants by engineered CRISPR-Cas endonucleases
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作者 Tom Schreiber Anja Prange +7 位作者 Petra Schafer Thomas Iwen Ramona Grutzner Sylvestre Marillonnet aurelie lepage Marie Javelle Wyatt Paul Alain Tissier 《Molecular Plant》 SCIE CSCD 2024年第5期824-837,共14页
In plants and mammals,non-homologous end-joining is the dominant pathway to repair DNA doublestrand breaks,making it challenging to generate knock-in events.In this study,we identified two groups of exonucleases from ... In plants and mammals,non-homologous end-joining is the dominant pathway to repair DNA doublestrand breaks,making it challenging to generate knock-in events.In this study,we identified two groups of exonucleases from the herpes virus and the bacteriophage T7 families that conferred an up to 38-fold increase in homology-directed repair frequencies when fused to Cas9/Cas12a in a tobacco mosaic virus-based transient assay in Nicotiana benthamiana.We achieved precise and scar-free insertion of several kilobases of DNA both in transient and stable transformation systems.In Arabidopsis thaliana,fusion of Cas9 to a herpes virus family exonuclease led to 10-fold higher frequencies of knock-ins in the first generation of transformants.In addition,we demonstrated stable and heritable knock-ins in wheat in 1%of the primary transformants.Taken together,our results open perspectives for the routine production of heritable knock-in and gene replacement events in plants. 展开更多
关键词 homology-directed repair knockin gene replacement CRISPR-Cas 50 exonuclease PLANTS
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