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Efficient and versatile multiplex prime editing in hexaploid wheat

Prime editing is limited by low efficiency in plants. Here, we develop an upgraded engineered plant prime editor in hexaploid wheat, ePPEplus, by introducing a V223A substitution into reverse transcriptase in the ePPEmax* architecture. ePPEplus enhances the efficiency by an average 33.0-fold and 6.4...

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Detalles Bibliográficos
Autores principales: Ni, Pei, Zhao, Yidi, Zhou, Ximeng, Liu, Zehua, Huang, Zhengwei, Ni, Zhongfu, Sun, Qixin, Zong, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308706/
https://www.ncbi.nlm.nih.gov/pubmed/37386475
http://dx.doi.org/10.1186/s13059-023-02990-1
Descripción
Sumario:Prime editing is limited by low efficiency in plants. Here, we develop an upgraded engineered plant prime editor in hexaploid wheat, ePPEplus, by introducing a V223A substitution into reverse transcriptase in the ePPEmax* architecture. ePPEplus enhances the efficiency by an average 33.0-fold and 6.4-fold compared to the original PPE and ePPE, respectively. Importantly, a robust multiplex prime editing platform is established for simultaneous editing of four to ten genes in protoplasts and up to eight genes in regenerated wheat plants at frequencies up to 74.5%, thus expanding the applicability of prime editors for stacking of multiple agronomic traits. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-02990-1.