Baksa Ivett, Nagy Tibor, Barta Endre, Havelda Zoltán, Várallyay Éva, Silhavy Dániel, Burgyán József, Szittya György
Institute of Plant Biotechnology, National Agricultural Research and Innovation Centre, Agricultural Biotechnology Institute, Szent-Györgyi Albert ut 4, H-2100, Gödöllő, Hungary.
BMC Genomics. 2015 Dec 1;16:1025. doi: 10.1186/s12864-015-2209-6.
Nicotiana benthamiana is a widely used model plant species for research on plant-pathogen interactions as well as other areas of plant science. It can be easily transformed or agroinfiltrated, therefore it is commonly used in studies requiring protein localization, interaction, or plant-based systems for protein expression and purification. To discover and characterize the miRNAs and their cleaved target mRNAs in N. benthamiana, we sequenced small RNA transcriptomes and degradomes of two N. benthamiana accessions and validated them by Northern blots.
We used a comprehensive molecular approach to detect and to experimentally validate N. benthamiana miRNAs and their target mRNAs from various tissues. We identified 40 conserved miRNA families and 18 novel microRNA candidates and validated their target mRNAs with a genomic scale approach. The accumulation of thirteen novel miRNAs was confirmed by Northern blot analysis. The conserved and novel miRNA targets were found to be involved in various biological processes including transcription, RNA binding, DNA modification, signal transduction, stress response and metabolic process. Among the novel miRNA targets we found the mRNA of REPRESSOR OF SILENCING (ROS1). Regulation of ROS1 by a miRNA provides a new regulatory layer to reinforce transcriptional gene silencing by a post-transcriptional repression of ROS1 activity.
The identified conserved and novel miRNAs along with their target mRNAs also provides a tissue specific atlas of known and new miRNA expression and their cleaved target mRNAs of N. benthamiana. Thus this study will serve as a valuable resource to the plant research community that will be beneficial well into the future.
本氏烟草是一种广泛用于植物 - 病原体相互作用以及植物科学其他领域研究的模式植物物种。它易于转化或进行农杆菌浸润,因此常用于需要蛋白质定位、相互作用或基于植物的蛋白质表达和纯化系统的研究。为了发现和鉴定本氏烟草中的微小RNA(miRNA)及其切割的靶标信使核糖核酸(mRNA),我们对两个本氏烟草种质的小RNA转录组和降解组进行了测序,并通过Northern杂交进行了验证。
我们采用综合分子方法从各种组织中检测并实验验证本氏烟草的miRNA及其靶标mRNA。我们鉴定出40个保守的miRNA家族和18个新的微小RNA候选物,并采用基因组规模方法验证了它们的靶标mRNA。通过Northern杂交分析证实了13个新miRNA的积累。发现保守和新的miRNA靶标参与各种生物学过程,包括转录、RNA结合、DNA修饰、信号转导、应激反应和代谢过程。在新的miRNA靶标中,我们发现了沉默抑制因子(ROS1)的mRNA。miRNA对ROS1的调控提供了一个新的调控层面,通过对ROS1活性的转录后抑制来加强转录基因沉默。
鉴定出的保守和新miRNA及其靶标mRNA还提供了本氏烟草已知和新miRNA表达及其切割靶标mRNA的组织特异性图谱。因此,本研究将成为植物研究界的宝贵资源,在未来很长一段时间内都将发挥有益作用。