Patil Basavaprabhu L, Fauquet Claude M
Donald Danforth Plant Science Center, 975 N. Warson Rd., St. Louis, MO, 63132, USA; National Research Centre on Plant Biotechnology, IARI, Pusa Campus, New Delhi, 110012, India.
Mol Plant Pathol. 2015 Jun;16(5):484-94. doi: 10.1111/mpp.12205. Epub 2014 Oct 27.
RNA silencing is a sequence-specific post-transcriptional gene inactivation mechanism that operates in diverse organisms and that can extend beyond its site of initiation, owing to the movement of the silencing signal, called non-autonomous gene silencing. Previous studies have shown that several factors manifest the movement of the silencing signal, such as the size (21 or 24 nucleotides) of the secondary small interfering RNA (siRNA) produced, the steady-state concentration of siRNAs and their cognate messenger RNA (mRNA) or a change in the sink-source status of plant parts affecting phloem translocation. Our study shows that both light intensity and temperature have a significant impact on the systemic movement of the silencing signal in transient agroinfiltration studies in Nicotiana benthamiana. At higher light intensities (≥ 450 μE/m(2)/s) and higher temperatures (≥ 30 °C), gene silencing was localized to leaf tissue that was infiltrated, without any systemic spread. Interestingly, in these light and temperature conditions (≥ 450 μE/m(2) /s and ≥ 30 °C), the N. benthamiana plants showed recovery from the viral symptoms. However, the reduced systemic silencing and reduced viral symptom severity at higher light intensities were caused by a change in the sink-source status of the plant, ultimately affecting the phloem translocation of small RNAs or the viral genome. In contrast, at lower light intensities (<300 μE/m(2)/s) with a constant temperature of 25 °C, there was strong systemic movement of the silencing signal in the N. benthamiana plants and reduced recovery from virus infections. The accumulation of gene-specific siRNAs was reduced at higher temperature as a result of a reduction in the accumulation of transcript on transient agroinfiltration of RNA interference (RNAi) constructs, mostly because of poor T-DNA transfer activity of Agrobacterium, possibly also accompanied by reduced phloem translocation.
RNA沉默是一种序列特异性的转录后基因失活机制,存在于多种生物体中,并且由于沉默信号(称为非自主基因沉默)的移动,这种机制可以延伸到其起始位点之外。先前的研究表明,有几个因素表明了沉默信号的移动,例如产生的二级小干扰RNA(siRNA)的大小(21或24个核苷酸)、siRNA及其同源信使RNA(mRNA)的稳态浓度,或者影响韧皮部转运的植物部位源库状态的变化。我们的研究表明,在本氏烟草的瞬时农杆菌浸润研究中,光照强度和温度对沉默信号的系统移动都有显著影响。在较高光照强度(≥450 μE/m²/s)和较高温度(≥30°C)下,基因沉默局限于浸润的叶片组织,没有任何系统传播。有趣的是,在这些光照和温度条件(≥450 μE/m²/s和≥30°C)下,本氏烟草植株表现出从病毒症状中恢复。然而,较高光照强度下系统沉默的减少和病毒症状严重程度的降低是由植物源库状态的变化引起的,最终影响了小RNA或病毒基因组的韧皮部转运。相比之下,在25°C恒温且较低光照强度(<300 μE/m²/s)下,本氏烟草植株中沉默信号有强烈的系统移动,且从病毒感染中恢复的能力降低。由于RNA干扰(RNAi)构建体瞬时农杆菌浸润时转录本积累减少,导致较高温度下基因特异性siRNA的积累减少,这主要是因为农杆菌的T-DNA转移活性较差,也可能伴随着韧皮部转运减少。