首页> 美国卫生研究院文献>Springer Open Choice >Amplicon-Based RNA Interference Targeting V2 Gene of Cotton Leaf Curl Kokhran Virus-Burewala Strain Can Provide Resistance in Transgenic Cotton Plants
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Amplicon-Based RNA Interference Targeting V2 Gene of Cotton Leaf Curl Kokhran Virus-Burewala Strain Can Provide Resistance in Transgenic Cotton Plants

机译:基于扩增子的RNA干扰靶向棉花叶卷毛Kokhran病毒-Burewala株的V2基因可以在转基因棉花植物中提供抗性

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摘要

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 0, T 1, and T 2 generations using gene-specific primers. Transgenic cotton plants were categorized on the basis of the virus disease index in T 1 generation. Copy number and transgene location were observed using FISH and karyotyping in T 2 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.
机译:begomoviruses的保守外壳或V2基因负责植物细胞中的病毒移动。 RNAi技术被用于沉默V2基因,以抵抗转基因植物中的这些病毒。在35S启动子下克隆的靶向CLCuKoV-Bur V2基因的基于RNAi的基因构建体的转化,采用了先端切变法,在两个优良棉花品种MNH-786和VH-289中进行。发现MNH-786和VH-289的转化效率分别为3.75%和2.88%。使用基因特异性引物通过PCR在T 0,T 1和T 2世代中完成成功转化的确认。根据T 1代中的病毒疾病指数对转基因棉花进行分类。在第2代中使用FISH和核型分析观察到拷贝数和转基因位置,这证实了V2 RNAi扩增子在6号和16号染色体上的随机整合。与野生型对照植物相比,有前景的转基因品系的实时定量PCR分析显示病毒效价低在封闭的环境中用有毒的粉虱挑战它们。从结果可以得出结论,扩增子V2 RNAi构建体能够限制病毒复制,并且可以用于现场控制CLCuV。

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