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利用 RNAi 技术开发抗 PRSV 转基因木瓜。

Use of RNAi technology to develop a PRSV-resistant transgenic papaya.

机构信息

Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agriculture Sciences, 571101, Haikou, Hainan, China.

Hawaii Agriculture Research Center, 96797, Waipahu, HI, USA.

出版信息

Sci Rep. 2017 Oct 3;7(1):12636. doi: 10.1038/s41598-017-13049-0.

Abstract

Papaya ringspot virus (PRSV) seriously limits papaya (Carica papaya L.) production in tropical and subtropical areas throughout the world. Coat protein (CP)- transgenic papaya lines resistant to PRSV isolates in the sequence-homology-dependent manner have been developed in the U.S.A. and Taiwan. A previous investigation revealed that genetic divergence among Hainan isolates of PRSV has allowed the virus to overcome the CP-mediated transgenic resistance. In this study, we designed a comprehensive RNAi strategy targeting the conserved domain of the PRSV CP gene to develop a broader-spectrum transgenic resistance to the Hainan PRSV isolates. We used an optimized particle-bombardment transformation system to produce RNAi-CP-transgenic papaya lines. Southern blot analysis and Droplet Digital PCR revealed that line 474 contained a single transgene insert. Challenging this line with different viruses (PRSV I, II and III subgroup) under greenhouse conditions validated the transgenic resistance of line 474 to the Hainan isolates. Northern blot analysis detected the siRNAs products in virus-free transgenic papaya tissue culture seedlings. The siRNAs also accumulated in PRSV infected transgenic papaya lines. Our results indicated that this transgenic papaya line has a useful application against PRSV in the major growing area of Hainan, China.

摘要

番木瓜环斑病毒(PRSV)严重限制了全球热带和亚热带地区的番木瓜(Carica papaya L.)生产。美国和中国台湾已开发出针对 PRSV 分离株的序列同源依赖性衣壳蛋白(CP)转基因番木瓜系,具有抗性。先前的研究表明,PRSV 海南分离株之间的遗传差异使该病毒能够克服 CP 介导的转基因抗性。在这项研究中,我们设计了一种针对 PRSV CP 基因保守结构域的综合 RNAi 策略,以开发对海南 PRSV 分离株具有更广泛谱的转基因抗性。我们使用优化的粒子轰击转化系统来生产 RNAi-CP-转基因番木瓜系。Southern blot 分析和 Droplet Digital PCR 显示,474 号线含有一个转基因插入片段。在温室条件下用不同病毒(PRSV I、II 和 III 亚组)对该系进行挑战,验证了 474 号线对海南分离株的转基因抗性。Northern blot 分析检测到无病毒转基因番木瓜组织培养苗中的 siRNAs 产物。siRNAs 也在感染 PRSV 的转基因番木瓜系中积累。我们的结果表明,该转基因番木瓜系在中国海南主要种植区对 PRSV 具有有用的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eadb/5626737/07fab33ba4a9/41598_2017_13049_Fig1_HTML.jpg

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