Jain Heena, Kaur Ramandeep, Sain Satish Kumar, Siwach Priyanka
Department of Biotechnology, Chaudhary Devi Lal University, Sirsa, Haryana 125055 India.
Central Institute of Cotton Research, Regional Station, Sirsa, Haryana 125055 India.
Indian J Microbiol. 2024 Jun;64(2):558-571. doi: 10.1007/s12088-024-01191-z. Epub 2024 Feb 3.
Cotton leaf curl disease (CLCuD), caused by the Cotton leaf curl virus, is one of the most irrepressible diseases in cotton due to high recombination in the virus. RNA interference (RNAi) is widely used as a biotechnological approach for sequence-specific gene silencing guided by small interfering RNAs (siRNAs) to generate resistance against viruses. The success of RNAi depends upon the fact that the target site of the designed siRNA must be conserved even if the genome undergoes recombination. Thus, the present study designs the most efficient siRNA against the conserved sites of the Cotton leaf curl Multan virus (CLCuMuV) and the Cotton leaf curl Multan betasatellite (CLCuMB). From an initial prediction of 9 and 7 siRNAs against CLCuMuV and CLCuMB, respectively, the final selection was made for 2 and 1 siRNA based on parameters such as no off-targets, good GC content, high validity score, and targeting coding region. The target sites of siRNA were observed to lie in the AC3 and an overlapping region of AC2-AC1 of CLCuMuV and βC1 of CLCuMB; all target sites showed a highly conserved nature in recombination analysis. Docking the designed siRNAs with the Argonaute-2 protein of showed stable binding. Finally, BLASTn of siRNA-target positions in genomes of other BGVs indicated the suitability of designed siRNAs against a broad range of BGVs. The designed siRNAs of the present study could help gain complete control over the virus, though experimental validation is highly required to suggest predicted siRNAs for CLCuD resistance.
The online version contains supplementary material available at 10.1007/s12088-024-01191-z.
由棉花卷叶病毒引起的棉花卷叶病(CLCuD)是棉花中最难控制的病害之一,原因是该病毒具有高度重组性。RNA干扰(RNAi)作为一种生物技术方法被广泛应用,通过小干扰RNA(siRNA)引导进行序列特异性基因沉默,以产生抗病毒抗性。RNAi的成功取决于这样一个事实,即即使基因组发生重组,设计的siRNA的靶位点也必须保守。因此,本研究针对棉花卷叶木尔坦病毒(CLCuMuV)和棉花卷叶木尔坦β卫星(CLCuMB)的保守位点设计了最有效的siRNA。从最初分别针对CLCuMuV和CLCuMB预测的9个和7个siRNA中,基于无脱靶、良好的GC含量、高有效性评分和靶向编码区等参数,最终选择了2个和1个siRNA。观察到siRNA的靶位点位于CLCuMuV的AC3以及AC2 - AC1的重叠区域和CLCuMB的βC1;在重组分析中,所有靶位点都表现出高度保守的性质。将设计的siRNA与Argonaute - 2蛋白对接显示出稳定的结合。最后,对其他BGVs基因组中siRNA靶位点的BLASTn分析表明,设计的siRNA适用于广泛的BGVs。本研究设计的siRNA有助于全面控制该病毒,不过仍高度需要进行实验验证,以推荐用于CLCuD抗性的预测siRNA。
在线版本包含可在10.1007/s12088 - 024 - 01191 - z获取的补充材料。