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基于扩增子的RNA干扰靶向棉花曲叶科克伦病毒-布勒瓦拉株系的V2基因可使转基因棉花植株产生抗性。

Amplicon-Based RNA Interference Targeting V2 Gene of Cotton Leaf Curl Kokhran Virus-Burewala Strain Can Provide Resistance in Transgenic Cotton Plants.

作者信息

Yasmeen Aneela, Kiani Sarfraz, Butt Afshan, Rao Abdul Qayyum, Akram Faheem, Ahmad Aftab, Nasir Idrees Ahmad, Husnain Tayyab, Mansoor Shahid, Amin Imran, Aftab Shaheen, Zubair Muhammad, Tahir Muhammad Nouman, Akhtar Sohail, Scheffler Jodi, Scheffler Brian

机构信息

Center of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore, Pakistan.

National Institute of Biotechnology and Genetic Engineering, Faisalabad, Pakistan.

出版信息

Mol Biotechnol. 2016 Dec;58(12):807-820. doi: 10.1007/s12033-016-9980-8.

Abstract

The conserved coat or V2 gene of begomoviruses is responsible for viral movement in the plant cells. RNAi technology was used to silence V2 gene for resistance against these viruses in transgenic plants. The transformation of the RNAi-based gene construct targeting V2 gene of CLCuKoV-Bur, cloned under 35S promoter, was done in two elite cotton varieties MNH-786 and VH-289 using shoot apex cut method of gene transformation. The transformation efficiency was found to be 3.75 and 2.88 % in MNH-786 and VH-289, respectively. Confirmation of successful transformation was done through PCR in T , T , and T generations using gene-specific primers. Transgenic cotton plants were categorized on the basis of the virus disease index in T generation. Copy number and transgene location were observed using FISH and karyotyping in T generation which confirmed random integration of V2 RNAi amplicon at chromosome 6 and 16. Real-time quantitative PCR analyses of promising transgenic lines showed low virus titer compared to wild-type control plants upon challenging them with viruliferous whiteflies in a contained environment. From the results, it was concluded that amplicon V2 RNAi construct was able to limit virus replication and can be used to control CLCuV in the field.

摘要

双生病毒保守的外壳蛋白或V2基因负责病毒在植物细胞中的移动。RNA干扰技术被用于使V2基因沉默,以赋予转基因植物对这些病毒的抗性。以RNA干扰为基础、靶向棉花曲叶柯枝病毒(CLCuKoV-Bur)V2基因的基因构建体,克隆于35S启动子之下,采用茎尖切割基因转化法,在两个优良棉花品种MNH-786和VH-289中进行转化。结果发现,在MNH-786和VH-289中的转化效率分别为3.75%和2.88%。利用基因特异性引物,通过对T₀、T₁和T₂代进行PCR,确认转化成功。在T₂代,根据病毒病指数对转基因棉花植株进行分类。在T₂代,利用荧光原位杂交(FISH)和核型分析观察拷贝数和转基因定位,证实V2 RNA干扰扩增子随机整合到第6号和第16号染色体上。对有前景的转基因株系进行实时定量PCR分析,结果显示,在封闭环境中用带毒粉虱对其进行挑战时,与野生型对照植株相比,病毒滴度较低。从结果可以得出结论,扩增子V2 RNA干扰构建体能够限制病毒复制,可用于田间防治棉花曲叶病毒(CLCuV)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74e/5102983/5418dfca9d00/12033_2016_9980_Fig1_HTML.jpg

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