Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, 53700, Pakistan.
Department of Microbiology, BUITEMS, Quetta, Pakistan.
Transgenic Res. 2018 Apr;27(2):203-210. doi: 10.1007/s11248-018-0066-1. Epub 2018 Feb 28.
RNA interference (RNAi) is commonly used to produce virus tolerant transgenic plants. The objective of the current study was to generate transgenic sugarcane plants expressing a short hairpin RNAs (shRNA) targeting the coat protein (CP) gene of sugarcane mosaic virus (SCMV). Based on multiple sequence alignment, including genomic sequences of four SCMV strains, a conserved region of ~ 456 bp coat protein (CP) gene was selected as target gene and amplified through polymerase chain reaction (PCR). Subsequently, siRNAs2 and siRNA4 were engineered as stable short hairpin (shRNA) transgenes of 110 bp with stem and loop sequences derived from microRNA (sof-MIR168a; an active regulatory miRNA in sugarcane). These transgenes were cloned in independent RNAi constructs under the control of the polyubiquitin promoter. The RNAi constructs were delivered into two sugarcane cultivars 'SPF-234 and NSG-311 in independent experiments using particle bombardment. Molecular identification through PCR and Southern blot revealed anti-SCMV positive transgenic lines. Upon mechanical inoculation of transgenic and non-transgenic sugarcane lines with SCMV, the degree of resistance was found variable among the two sugarcane cultivars. For sugarcane cultivar NSG-311, the mRNA expression of the CP-SCMV was reduced to 10% in shRNA2-transgenic lines and 80% in shRNA4-transgenic lines. In sugarcane cultivar SPF-234, the mRNA expression of the CP-SCMV was reduced to 20% in shRNA2-transgenic lines and 90% in shRNA4 transgenic lines, revealing that transgenic plants expressing shRNA4 were almost immune to SCMV infection.
RNA 干扰(RNAi)通常用于生产具有病毒耐受性的转基因植物。本研究的目的是生成表达靶向甘蔗花叶病毒(SCMV)外壳蛋白(CP)基因的短发夹 RNA(shRNA)的转基因甘蔗植物。基于包括四个 SCMV 株系基因组序列的多重序列比对,选择了一个约 456bp 的外壳蛋白(CP)基因保守区作为靶基因,并通过聚合酶链反应(PCR)进行扩增。随后,将 siRNAs2 和 siRNA4 设计为具有茎环序列的稳定短发夹(shRNA)转基因物,其茎环序列来自 microRNA(sof-MIR168a;甘蔗中一种活跃的调控 miRNA)。这些转基因物在聚泛素启动子的控制下克隆在独立的 RNAi 构建体中。通过粒子轰击在两个甘蔗品种 'SPF-234 和 NSG-311 中独立进行了 RNAi 构建体的递送实验。通过 PCR 和 Southern blot 进行的分子鉴定显示出抗 SCMV 的阳性转基因系。在对转基因和非转基因甘蔗系进行机械接种 SCMV 后,发现两个甘蔗品种的抗性程度不同。对于甘蔗品种 NSG-311,shRNA2 转基因系中 CP-SCMV 的 mRNA 表达减少到 10%,shRNA4 转基因系中减少到 80%。在甘蔗品种 SPF-234 中,shRNA2 转基因系中 CP-SCMV 的 mRNA 表达减少到 20%,shRNA4 转基因系中减少到 90%,表明表达 shRNA4 的转基因植物几乎对 SCMV 感染具有免疫力。