Tuttle John R, Haigler Candace H, Robertson Dominique Niki
Department of Crop Science, North Carolina State University, Box 7620, Raleigh, NC, 27695-7620, USA.
Methods Mol Biol. 2015;1287:219-34. doi: 10.1007/978-1-4939-2453-0_16.
Virus-Induced Gene Silencing (VIGS) is a useful method for transient downregulation of gene expression in crop plants. The geminivirus Cotton leaf crumple virus (CLCrV) has been modified to serve as a VIGS vector for persistent gene silencing in cotton. Here the use of Green Fluorescent Protein (GFP) is described as a marker for identifying silenced tissues in reproductive tissues, a procedure that requires the use of transgenic plants. Suggestions are given for isolating and cloning combinations of target and marker sequences so that the total length of inserted foreign DNA is between 500 and 750 bp. Using this strategy, extensive silencing is achieved with only 200-400 bp of sequence homologous to an endogenous gene, reducing the possibility of off-target silencing. Cotyledons can be inoculated using either the gene gun or Agrobacterium and will continue to show silencing throughout fruit and fiber development. CLCrV is not transmitted through seed, and VIGS is limited to genes expressed in the maternally derived seed coat and fiber in the developing seed. This complicates the use of GFP as a marker for VIGS because cotton fibers must be separated from unsilenced tissue in the seed to determine if they are silenced. Nevertheless, fibers from a large number of seeds can be rapidly screened following placement into 96-well plates. Methods for quantifying the extent of silencing using semiquantitative RT-PCR are given.
病毒诱导的基因沉默(VIGS)是一种用于瞬时下调作物植物基因表达的有用方法。双生病毒棉花叶皱缩病毒(CLCrV)已被改造用作VIGS载体,用于棉花中的持久性基因沉默。本文描述了使用绿色荧光蛋白(GFP)作为标记来鉴定生殖组织中沉默的组织,该过程需要使用转基因植物。文中给出了分离和克隆靶标序列与标记序列组合的建议,以使插入的外源DNA总长度在500至750bp之间。使用这种策略,仅用200 - 400bp与内源基因同源的序列就能实现广泛的沉默,降低了脱靶沉默的可能性。子叶可以使用基因枪或农杆菌进行接种,并且在整个果实和纤维发育过程中都将持续显示沉默。CLCrV不会通过种子传播,并且VIGS仅限于在发育种子中母本来源的种皮和纤维中表达的基因。这使得GFP作为VIGS标记的使用变得复杂,因为必须将棉纤维与种子中未沉默的组织分离,以确定它们是否被沉默。然而,将大量种子的纤维放入96孔板后,可以快速进行筛选。文中给出了使用半定量RT-PCR定量沉默程度的方法。