Abstract

Viroids are plant-pathogenic molecules made up of single-stranded circular non-coding RNAs. How replicating viroids interfere with host silencing remains largely unknown. In this study, we investigated the effects of a nuclear-replicating Potato spindle tuber viroid (PSTVd) on interference with plant RNA silencing. Using transient induction of silencing in GFP transgenic Nicotiana benthamiana plants (line 16c), we found that PSTVd replication accelerated GFP silencing and increased Virp1 mRNA, which encodes bromodomain-containing viroid-binding protein 1 and is required for PSTVd replication. DNA methylation was increased in the GFP transgene promoter of PSTVd-replicating plants, indicating involvement of transcriptional gene silencing. Consistently, accelerated GFP silencing and increased DNA methylation in the of GFP transgene promoter were detected in plants transiently expressing Virp1. Virp1 mRNA was also increased upon PSTVd infection in natural host potato plants. Reduced transcript levels of certain endogenous genes were also consistent with increases in DNA methylation in related gene promoters in PSTVd-infected potato plants. Together, our data demonstrate that PSTVd replication interferes with the nuclear silencing pathway in that host plant, and this is at least partially attributable to Virp1. This study provides new insights into the plant-viroid interaction on viroid pathogenicity by subverting the plant cell silencing machinery.

Highlights

  • Many eukaryotes share highly abundant classes of small RNAs that range in size from 20 to 25 nucleotides produced from longer double-stranded RNA precursors through the action of RNase III-like Dicer or Dicer-like (DCL) enzymes[1,2]

  • We showed that Potato spindle tuber viroid (PSTVd) infection in N. benthamiana and its natural host potato plants triggered RNA silencing and produced a large amount of siRNA derived from PSTVd (siPSTVd)

  • Our results show that PSTVd replication in both N. benthamiana and potato plants induced Virp[1] and enhanced gene silencing by interfering with DNA methylation

Read more

Summary

Introduction

Many eukaryotes share highly abundant classes of small RNAs (sRNAs) that range in size from 20 to 25 nucleotides (nt) produced from longer double-stranded RNA (dsRNA) precursors through the action of RNase III-like Dicer or Dicer-like (DCL) enzymes[1,2]. The sRNAs participate in RNA silencing (or RNA interference, RNAi) by binding to an ARGONAUTE (AGO) protein in RNA-induced silencing complexes (RISCs) and act as sequence-specificity determinants through RNA-RNA and RNA-DNA interactions. The TGS pathway consists of RNA-directed DNA methylation (RdDM), which requires both 24-nt small interfering RNAs (siRNAs) and long non-coding RNA transcripts as well as proteins, such as DNA-dependent RNA polymerase IV (Pol IV), RNA-dependent RNA polymerase 2 (RDR2) and AGO4 for de novo DNA methylation. This pathway has a great impact on the expression and constitution of the plant genome[5]. Our results demonstrate that the host Viroid-binding bromodomain-containing protein, Virp[1], which is required and induced by PSTVd infection, may partially contribute to the interference of the nuclear silencing pathway in PSTVd-infected plants

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call