Plant Virology Institute CNR (IVV), Grugliasco Unit., 10095 Grugliasco-TO, Italy.
Transgenic Res. 2010 Feb;19(1):17-27. doi: 10.1007/s11248-009-9289-5. Epub 2009 Jun 9.
Eight transgenic grapevine lines transformed with the coat protein gene of Grapevine fanleaf virus (GFLV-CP) were analyzed for a correlation between transgene expression, siRNAs production and DNA methylation. Bisulphite genome sequencing was used for a comprehensive analysis of DNA methylation. Methylated cytosine residues of CpG and CpNpG sites were detected in the GFLV-CP transgene, in the T7 terminator and in the 35S promoter of three grapevines without transgene expression, but no detectable level of siRNAs was recorded in these lines. The detailed analysis of 8 lines revealed the complex arrangements of T-DNA and integrated binary vector sequences as crucial factors that influence transgene expression. After inoculation with GFLV, no change in the levels of cytosine methylation was observed, but transgenic and untransformed plants produced short siRNAs (21-22 nt) indicating that the grapevine plants responded to GFLV infection by activating a post-transcriptional gene silencing mechanism.
对 8 个转染了葡萄扇叶病毒(GFLV)外壳蛋白基因的转基因葡萄品系进行分析,以研究转基因表达、siRNA 产生和 DNA 甲基化之间的相关性。亚硫酸氢盐基因组测序用于全面分析 DNA 甲基化。在没有转基因表达的 3 个葡萄品种的 GFLV-CP 转基因、T7 终止子和 35S 启动子中检测到 CpG 和 CpNpG 位点的甲基化胞嘧啶残基,但在这些品系中未检测到可检测水平的 siRNA。对 8 条品系的详细分析表明,T-DNA 和整合的二元载体序列的复杂排列是影响转基因表达的关键因素。接种 GFLV 后,未观察到胞嘧啶甲基化水平的变化,但转基因和非转基因植物产生了短 siRNA(21-22nt),表明葡萄植物通过激活转录后基因沉默机制对 GFLV 感染作出反应。