Involvement of RDR6 in short-range intercellular RNA silencing in Nicotiana benthamiana

In plants, non-cell autonomous RNA silencing spreads between cells and over long distances. Recent work has revealed insight on the genetic and molecular components essential for cell-to-cell movement of RNA silencing in Arabidopsis. Using a local RNA silencing assay, we report on a distinct mechanism that may govern the short-range (6–10 cell) trafficking of virus-induced RNA silencing from epidermal to neighbouring palisade and spongy parenchyma cells in Nicotiana benthamiana. This process involves a previously unrecognised function of the RNA-dependent RNA polymerase 6 (RDR6) gene. Our data suggest that plants may have evolved distinct genetic controls in intercellular RNA silencing among different types of cells

Antiviral Silencing and Suppression of Gene Silencing in Plants

RNA silencing is an evolutionary conserved sequence-specific gene inactivation mechanism that contributes to the control of development, maintains heterochromatin, acts in stress responses, DNA repair and defends against invading nucleic acids like transposons and viruses. In plants RNA silencing functions as one of the main immune systems. RNA silencing process involves the small RNAs and trans factor components like Dicers, Argonautes and RNA-dependent RNA poly- merases. To deal with host antiviral silencing responses viruses evolved mecha- nisms to avoid or counteract this, most notably through expression of viral suppressors of RNA silencing. Due to the overlap between endogenous and antiviral silencing pathways while blocking antiviral pathways viruses also impact endogenous silencing processes. Here we provide an overview of antiviral silencing pathway, host factors implicated in it and the crosstalk between antiviral and endogenous branches of silencing. We summarize the current status of knowledge about the viral counter-defense strategies acting at various steps during virus infection in plants with the focus on representative, well studied silencing suppres- sor proteins. Finally we discuss future challenges of the antiviral silencing and counter-defense research field

EFFECTS OF TYROSINE AND PLANT GROWTH REGULATORS ON GROWTH AND DEVELOPMENT OF GLORIOSA SUPERBA LINN., A MEDICINAL PLANT, IN VITRO

The study of effects of tyrosine and plant growth regulators on rhizome cultures was carried out on modified Murashige Skoog medium. The sterile rhizomes were cut and cultured on MS medium, supplemented with 1 mg/l 2,4-D, 1 mg/l BA and various concentrations of tyrosine under light and dark condition. The experimental data showed that the highest percentage of callus formation was on the medium with 50 mg/l tyrosine, in the dark condition (100%) and in the light condition (85%). The average fresh weight of callus cultured in the dark for 16 weeks was 6.25 g. Shoot induction was performed using the combination of NAA and BA for 36 weeks. The experimental data revealed that the shoot regeneration from callus was 100% on the medium with 4 mg/l BA and 4 mg/l NAA. Comparison among various concentrations of BA and NAA showed that shoot formation was 83% and 50% on the medium containing 4 mg/l BA and 4 mg/l kinetin, respectively. The chromosome number from the root tip obtained from the tissue culture was 2n = 22. Acknowledgements: Dept. of Biology, Khon Kaen University provided funding and all participants in this project

Virus-induced gene silencing as a reverse genetics tool to study gene function

Reverse genetics has proven to be a powerful approach to elucidating gene function in plants, particularly in Arabidopsis. Virus-induced gene silencing (VIGS) is one such method and achieves reductions in target gene expression as the vector moves into newly formed tissues of inoculated plants. VIGS is especially useful for plants that are recalcitrant for transformation and for genes that cause embryo lethality. VIGS provides rapid, transient knockdowns as a complement to other reverse genetics tools and can be used to screen sequences for RNAi prior to stable transformation. High-throughput, forward genetic screening is also possible by cloning libraries of short gene fragments directly into a VIGS plasmid DNA vector, inoculating, and then looking for a phenotype of interest. VIGS is especially useful for studying genes in crop species, which currently have few genetic resources. VIGS facilitates a rapid comparison of knockdown phenotypes of the same gene in different breeding lines or mutant backgrounds, as the same vector is easily inoculated into different plants. In this chapter, we briefly discuss how to choose or construct a VIGS vector and then how to design and carry out effective experiments using VIGS

A Laboratory-intensive Course on RNA Interference and Model Organisms

RNA interference (RNAi) is a powerful method to silence gene expression in a variety of organisms and is generating interest not only as a useful tool for research scientists but also as a novel class of therapeutics in clinical trials. Here, we report that undergraduate and graduate students with a basic molecular biology background were able to demonstrate conceptual knowledge and technical skills for using RNAi as a research tool upon completion of an intensive 8-wk RNAi course with a 2-h lecture and 5-h laboratory per week. Students were instructed on design of RNAi experiments in model organisms and perform multiweek laboratory sessions based on journal articles read and discussed in class. Using Nicotiana benthamiana, Caenorhabditis elegans, and mammalian cell culture, students analyzed the extent of silencing using both qualitative assessment of phenotypic variations and quantitative measurements of RNA levels or protein levels. We evaluated the course over two semesters, each with a separate instructor. In both semesters, we show students met expected learning outcomes as demonstrated by successful laboratory experiment results, as well as positive instructor assessments of exams and lab reports. Student self-assessments revealed increased confidence in conceptual knowledge and practical skills. Our data also suggest that the course is adaptable to different instructors with varying expertise

AGO1-miR173 complex initiates phased siRNA formation in plants

MicroRNA (miRNA)-guided cleavage initiates entry of primary transcripts into the transacting siRNA (tasiRNA) biogenesis pathway involving RNA-DEPENDENT RNA POLYMERASE6, DICER-LIKE4, and SUPPRESSOR OF GENE SILENCING3. Arabidopsis thaliana TAS1 and TAS2 families yield tasiRNA that form through miR173-guided initiation–cleavage of primary transcripts and target several transcripts encoding pentatricopeptide repeat proteins and proteins of unknown function. Here, the TAS1c locus was modified to produce synthetic (syn) tasiRNA to target an endogenous transcript encoding PHYTOENE DESATURASE and used to analyze the role of miR173 in routing of transcripts through the tasiRNA pathway. miR173 was unique from other miRNAs in its ability to initiate TAS1c-based syn-tasiRNA formation. A single miR173 target site was sufficient to route non-TAS transcripts into the pathway to yield phased siRNA. We also show that miR173 functions in association with ARGONAUTE 1 (AGO1) during TAS1 and TAS2 tasiRNA formation, and we provide data indicating that the miR173–AGO1 complex possesses unique functionality that many other miRNA–AGO1 complexes lack