Kodama Hiroaki, Umeyama Yukiko, Miyahara Taira, Oguchi Taichi, Tsujimoto Takashi, Ozeki Yoshihiro, Ogawa Takumi, Yamaguchi Yube, Ohta Daisaku
Graduate School of Horticulture, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.
Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8572, Japan.
Food Saf (Tokyo). 2022 Mar 4;10(1):13-31. doi: 10.14252/foodsafetyfscj.D-21-00012. eCollection 2022 Mar.
Grafting of commercial varieties onto transgenic stress-tolerant rootstocks is attractive approach, because fruit from the non-transgenic plant body does not contain foreign genes. RNA silencing can modulate gene expression and protect host plants from viruses and insects, and small RNAs (sRNAs), key molecules of RNA silencing, can move systemically. Here, to evaluate the safety of foods obtained from sRNA-recipient plant bodies, we investigated the effects of rootstock-derived sRNAs involved in mediating RNA-directed DNA methylation (RdDM) on non-transgenic scions. We used tobacco rootstocks showing RdDM against the cauliflower mosaic virus (CaMV) 35S promoter. When scions harboring CaMV 35S promoter sequence were grafted onto RdDM-inducing rootstocks, we found that RdDM-inducing sRNAs were only weakly transported from the rootstocks to the scion, and we observed a low level of DNA methylation of the CaMV 35S promoter in the scion. Next, wild-type (WT) tobacco scions were grafted onto RdDM-inducing rootstocks (designated NT) or WT rootstocks (designated NN), and scion leaves were subjected to multi-omics analyses. Our transcriptomic analysis detected 55 differentially expressed genes between the NT and NN samples. A principal component analysis of proteome profiles showed no significant differences. In the positive and negative modes of LC-ESI-MS and GC-EI-MS analyses, we found a large overlap between the metabolomic clusters of the NT and NN samples. In contrast, the negative mode of a LC-ESI-MS analysis showed separation of clusters of NT and NN metabolites, and we detected 6 peak groups that significantly differed. In conclusion, we found that grafting onto RdDM-inducing rootstocks caused a low-level transmission of sRNAs, resulting in limited DNA methylation in the scion. However, the causal relationships between sRNA transmission and the very slight changes in the transcriptomic and metabolomic profiles of the scions remains unclear. The safety assessment points for grafting with RdDM rootstocks are discussed.
将商业品种嫁接到转基因抗逆砧木上是一种有吸引力的方法,因为非转基因植株所结的果实不含外源基因。RNA沉默可以调节基因表达,并保护宿主植物免受病毒和昆虫侵害,而小RNA(sRNA)作为RNA沉默的关键分子,可以进行系统性移动。在此,为了评估从sRNA受体植株获得的食品的安全性,我们研究了参与介导RNA指导的DNA甲基化(RdDM)的砧木来源sRNA对非转基因接穗的影响。我们使用了对花椰菜花叶病毒(CaMV)35S启动子表现出RdDM的烟草砧木。当将携带CaMV 35S启动子序列的接穗嫁接到诱导RdDM的砧木上时,我们发现诱导RdDM的sRNA仅从砧木微弱地转运到接穗,并且我们观察到接穗中CaMV 35S启动子的DNA甲基化水平较低。接下来,将野生型(WT)烟草接穗嫁接到诱导RdDM的砧木(命名为NT)或WT砧木(命名为NN)上,并对接穗叶片进行多组学分析。我们的转录组分析检测到NT和NN样本之间有55个差异表达基因。蛋白质组图谱的主成分分析显示没有显著差异。在LC-ESI-MS和GC-EI-MS分析的正、负模式下,我们发现NT和NN样本的代谢组聚类之间有很大的重叠。相比之下,LC-ESI-MS分析的负模式显示NT和NN代谢物聚类分离,并且我们检测到6个有显著差异的峰组。总之,我们发现嫁接到诱导RdDM的砧木上会导致sRNA的低水平传递,从而使接穗中的DNA甲基化有限。然而,sRNA传递与接穗转录组和代谢组图谱中非常微小变化之间的因果关系仍不清楚。本文讨论了使用RdDM砧木进行嫁接的安全评估要点。