Abstract

RNA silencing pathways control eukaryotic gene expression transcriptionally or posttranscriptionally in a sequence-specific manner. In RNA silencing, the production of double-stranded RNA (dsRNA) gives rise to various classes of 20–24 nucleotide (nt) small RNAs (smRNAs). In Arabidopsis thaliana, smRNAs are often derived from long dsRNA molecules synthesized by one of the six genomically encoded RNA-dependent RNA Polymerase (RDR) proteins. However, the full complement of the RDR-dependent smRNAs and functions that these proteins and their RNA-binding cofactors play in plant RNA silencing has not been fully uncovered. To address this gap, we performed a global genomic analysis of all six RDRs and two of their cofactors to find new substrates for RDRs and targets of the resulting RDR-derived siRNAs to uncover new functions for these proteins in plants. Based on these analyses, we identified substrates for the three RDRγ clade proteins (RDR3–5), which had not been well-characterized previously. We also identified new substrates for the other three RDRs (RDR1, RDR2, and RDR6) as well as the RDR2 cofactor RNA-directed DNA methylation 12 (RDM12) and the RDR6 cofactor suppressor of gene silencing 3 (SGS3). These findings revealed that the target substrates of SGS3 are not limited to those solely utilized by RDR6, but that this protein seems to be a more general cofactor for the RDR family of proteins. Additionally, we found that RDR6 and SGS3 are involved in the production of smRNAs that target transcripts related to abiotic stresses, including water deprivation, salt stress, and ABA response, and as expected the levels of these mRNAs are increased in rdr6 and sgs3 mutant plants. Correspondingly, plants that lack these proteins (rdr6 and sgs3 mutants) are hypersensitive to ABA treatment, tolerant to high levels of PEG8000, and have a higher survival rate under salt treatment in comparison to wild-type plants. In total, our analyses have provided an extremely data-rich resource for uncovering new functions of RDR-dependent RNA silencing in plants, while also revealing a previously unexplored link between the RDR6/SGS3-dependent pathway and plant abiotic stress responses.

Highlights

  • In all eight mutants tested we identified a number of transcripts that had a significant decrease in small RNAs (smRNAs) read counts as compared to in Col-0 flower buds (Table 1)

  • We found that a large proportion of 21–22 nt smRNAs with 50 adenosine bias was lost in the rdr6 mutant, indicating RDR6 plays a crucial role in the biogenesis of this smRNA population

  • We provide insights into new substrates processed by RNA-dependent RNA Polymerase (RDR) resulting in smRNA biogenesis, new smRNA populations produced by RDRs, and global determination of targets of RDR-derived short interfering RNAs (siRNAs)

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Summary

Introduction

With 71% of the world’s population currently experiencing water scarcity [1] and the projected increase in human population to 12.3 billion people by 2100 [2], there is an urgent need to develop crops that can survive under stressful conditions to meet the future. The plant hormone abscisic acid (ABA) is a major regulator of plant response to abiotic stresses. Exogenous ABA treatment, a method universally applied to mimic abiotic stresses, causes stomata closure and induces the expression of stress-responsive genes [3,4]. Previous studies reported that small RNAs (smRNAs) can regulate the ABA signaling pathway and play critical roles in the stress tolerance of Arabidopsis thaliana (hereafter Arabidopsis) [5]. Some of the proteins involved in the synthesis of these populations of smRNAs are still unknown

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