Saxena Sangeeta, Singh Nidhi, Ranade S A, Babu Sunil G
Department of Biotechnology, Babasaheb Bhimrao Ambedkar University, VidyaVihar, Lucknow, India.
Virus Genes. 2011 Dec;43(3):409-34. doi: 10.1007/s11262-011-0649-x. Epub 2011 Aug 6.
Use of siRNA is a powerful methodology to particularly knockdown the targeted genes in a sequence specific manner. The potential of siRNA can be harnessed for silencing specific geminiviral genes in papaya and tomato plant hosts, thus making them resistant to the respective viruses. The challenge is in designing exogenous siRNA which can trigger silencing of viral genes irrespective of the genetic variability in different viral isolates and at the same time the selected siRNA does not target any plant gene (off target silencing). In this study, we have designed siRNA from the most conserved regions of viral coat protein (AV1) and replicase (AC1) genes retrieved from different isolates of geminiviruses infecting papaya (PLCV), and tomato (TLCV & TLCV, Northern India), so as to give a broad spectrum resistance and efficient silencing as it is highly homology-dependent strategy. Software siRNA finder (Ambion) was used on the selected conserved sequences in order to select only those putative siRNA oligonucleotides which fulfill all the basic criteria required as per the algorithm. Finally, a cross search using BLAST was performed to confirm that the designed siRNAs do not have any homology to plant genome sequences. The putative siRNA sequences thus designed to target essential genes of geminiviruses and introduced into the plants may facilitate developing papaya and tomato crops with generic resistance to geminiviruses.
使用小干扰RNA(siRNA)是一种强大的方法,能够以序列特异性方式特别有效地敲低靶向基因。可以利用siRNA的这种潜力来沉默番木瓜和番茄植物宿主中特定的双生病毒基因,从而使它们对相应病毒具有抗性。挑战在于设计外源性siRNA,它能够触发病毒基因的沉默,而不考虑不同病毒分离株中的遗传变异性,同时所选的siRNA不会靶向任何植物基因(脱靶沉默)。在本研究中,我们从感染番木瓜(PLCV)和番茄(TLCV及印度北部的TLCV)的双生病毒不同分离株中检索到的病毒外壳蛋白(AV1)和复制酶(AC1)基因的最保守区域设计了siRNA,以便产生广谱抗性和高效沉默,因为这是一种高度依赖同源性的策略。使用软件siRNA finder(Ambion)对选定的保守序列进行分析,以仅选择那些符合算法要求的所有基本标准的假定siRNA寡核苷酸。最后,使用BLAST进行交叉搜索,以确认设计的siRNA与植物基因组序列没有任何同源性。如此设计的靶向双生病毒必需基因并导入植物中的假定siRNA序列可能有助于培育对双生病毒具有通用抗性的番木瓜和番茄作物。