欢迎访问《植物保护学报》网站！

首页 | 期刊简介 |
编委会
编委会
青年编委会
| 道德声明 | 投稿指南 | 联系我们 | 期刊订阅 | English

利用CRISPR/Cas13a编辑技术获得马铃薯抗PVX植株

引用本文：涂振,钟子旸,陈汝豪,杨曼华,詹晓慧,陈家茹,马恢,聂碧华.利用CRISPR/Cas13a编辑技术获得马铃薯抗PVX植株.植物保护学报,2024,51(1):211-218

DOI：10.13802/j.cnki.zwbhxb.2024.2022112

摘要点击次数:

全文下载次数:

作者	单位	E-mail
涂振	华中农业大学园艺林学学院, 果蔬园艺作物种质创新与利用全国重点实验室, 农业农村部马铃薯生物学与生物技术重点实验室, 武汉 430070
钟子旸	华中农业大学园艺林学学院, 果蔬园艺作物种质创新与利用全国重点实验室, 农业农村部马铃薯生物学与生物技术重点实验室, 武汉 430070 恒敬合创生物医药 (浙江) 有限公司, 浙江嘉兴 314000
陈汝豪	华中农业大学园艺林学学院, 果蔬园艺作物种质创新与利用全国重点实验室, 农业农村部马铃薯生物学与生物技术重点实验室, 武汉 430070
杨曼华	华中农业大学园艺林学学院, 果蔬园艺作物种质创新与利用全国重点实验室, 农业农村部马铃薯生物学与生物技术重点实验室, 武汉 430070
詹晓慧	湖北大学生命科学学院, 省部共建生物催化与酶工程国家重点实验室, 武汉 430062
陈家茹	华中农业大学园艺林学学院, 果蔬园艺作物种质创新与利用全国重点实验室, 农业农村部马铃薯生物学与生物技术重点实验室, 武汉 430070
马恢	张家口市农业科学院马铃薯研究所, 河北张家口 075000
聂碧华	华中农业大学园艺林学学院, 果蔬园艺作物种质创新与利用全国重点实验室, 农业农村部马铃薯生物学与生物技术重点实验室, 武汉 430070	nbihua@mail.hzau.edu.cn

中文摘要:为探究利用CRISPR/Cas13a系统获得抗马铃薯X病毒（potato virus X，PVX）马铃薯的可行性，通过设计靶向PVX中TGBp1基因的小向导RNA（small guide RNA，sgRNA），构建CRISPR/Cas13a基因编辑载体，以马铃薯栽培种Désirée为受体材料进行稳定遗传转化，并通过机械摩擦接种法鉴定转基因植株对PVX的抗性。结果显示，成功构建了靶向PVX的PVX-Cas13a载体，并获得了表达Cas13a的转基因马铃薯植株，对其中3个高表达Cas13a的株系进行PVX抗性鉴定，发现在接种PVX 10~20 d后，转基因植株系统叶上无明显发病症状，且PVX积累量均显著低于未接种PVX对照。表明靶向PVX的CRISPR/Cas13a系统能够有效抑制该病毒的积累，这为马铃薯抗PVX育种提供了一条有效策略。

中文关键词:马铃薯基因编辑 CRISPR/Cas13a 马铃薯X病毒抗性鉴定

Generation of PVX resistant potato plants by CRISPR/Cas13a editing technology

Author Name	Affiliation	E-mail
Tu Zhen	Key Laboratory of Potato Biology and Biotechnology, Ministry of Agriculture and Rural Affairs National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops College of Horticulture & Forestry Sciences, Huazhong Agricultural University, Wuhan 430070, Hubei Province, China
Zhong Ziyang	Key Laboratory of Potato Biology and Biotechnology, Ministry of Agriculture and Rural Affairs National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops College of Horticulture & Forestry Sciences, Huazhong Agricultural University, Wuhan 430070, Hubei Province, China Virtu Pharmako (Zhejiang) Company Limited, Jiaxing 314000, Zhejiang Province, China
Chen Ruhao	Key Laboratory of Potato Biology and Biotechnology, Ministry of Agriculture and Rural Affairs National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops College of Horticulture & Forestry Sciences, Huazhong Agricultural University, Wuhan 430070, Hubei Province, China
Yang Manhua	Key Laboratory of Potato Biology and Biotechnology, Ministry of Agriculture and Rural Affairs National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops College of Horticulture & Forestry Sciences, Huazhong Agricultural University, Wuhan 430070, Hubei Province, China
Zhan Xiaohui	State Key Laboratory of Biocatalysis and Enzyme Engineering, School of Life Sciences, Hubei University, Wuhan 430062, Hubei Province, China
Chen Jiaru	Key Laboratory of Potato Biology and Biotechnology, Ministry of Agriculture and Rural Affairs National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops College of Horticulture & Forestry Sciences, Huazhong Agricultural University, Wuhan 430070, Hubei Province, China
Ma Hui	Institute of Potato Research, Zhangjiakou Academy of Agricultural Sciences, Zhangjiakou 075000, Hebei Province, China
Nie Bihua	Key Laboratory of Potato Biology and Biotechnology, Ministry of Agriculture and Rural Affairs National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops College of Horticulture & Forestry Sciences, Huazhong Agricultural University, Wuhan 430070, Hubei Province, China	nbihua@mail.hzau.edu.cn

Abstract:To investigate the feasibility of utilizing the CRISPR/Cas13a system to confer resistance against potato virus X (PVX) in Solanum tuberosum, a targeted small guide RNA (sgRNA) was designed to disrupt the TGBp1 gene of PVX and was employed in constructing a CRISPR/Cas13a geneediting vector. The potato cultivar Désirée was chosen for stable genetic transformation. The results showed that transgenic potato lines expressing Cas13a were successfully developed and subsequently subjected to assessment for PVX resistance via mechanical inoculation. Among the transgenic lines, three demonstrated robust Cas13a expression and exhibited resistance to PVX. These resistant lines displayed an absence of disease symptoms on systemically infected leaves and showcased a substantial reduction in PVX accumulation between 10 to 20 days post-inoculation. These findings underscore the potency of the CRISPR/Cas13a system in effectively targeting PVX, thereby impeding virus accumulation. This study delineated the promising potential of harnessing CRISPR/Cas13a as a viable strategy for breeding PVX-resistant potatoes.

keywords:potato gene editing CRISPR/Cas13a potato virus X resistance identification

查看全文查看/发表评论下载PDF阅读器