Abstract

BackgroundIntroduction of a transgene that transcribes RNA homologous to an endogenous gene in the plant genome can induce silencing of both genes, a phenomenon termed cosuppression. Cosuppression was first discovered in transgenic petunia plants transformed with the CHS-A gene encoding chalcone synthase, in which nonpigmented sectors in flowers or completely white flowers are produced. Some of the flower-color patterns observed in transgenic petunias having CHS-A cosuppression resemble those in existing nontransgenic varieties. Although the mechanism by which white sectors are generated in nontransgenic petunia is known to be due to RNA silencing of the CHS-A gene as in cosuppression, whether the same trigger(s) and/or pattern of RNA degradation are involved in these phenomena has not been known. Here, we addressed this question using deep-sequencing and bioinformatic analyses of small RNAs.ResultsWe analyzed short interfering RNAs (siRNAs) produced in nonpigmented sectors of petal tissues in transgenic petunia plants that have CHS-A cosuppression and a nontransgenic petunia variety Red Star, that has naturally occurring CHS-A RNA silencing. In both silencing systems, 21-nt and 22-nt siRNAs were the most and the second-most abundant size classes, respectively. CHS-A siRNA production was confined to exon 2, indicating that RNA degradation through the RNA silencing pathway occurred in this exon. Common siRNAs were detected in cosuppression and naturally occurring RNA silencing, and their ranks based on the number of siRNAs in these plants were correlated with each other. Noticeably, highly abundant siRNAs were common in these systems. Phased siRNAs were detected in multiple phases at multiple sites, and some of the ends of the regions that produced phased siRNAs were conserved.ConclusionsThe features of siRNA production found to be common to cosuppression and naturally occurring silencing of the CHS-A gene indicate mechanistic similarities between these silencing systems especially in the biosynthetic processes of siRNAs including cleavage of CHS-A transcripts and subsequent production of secondary siRNAs in exon 2. The data also suggest that these events occurred at multiple sites, which can be a feature of these silencing phenomena.

Highlights

  • Introduction of a transgene that transcribes RNA homologous to an endogenous gene in the plant genome can induce silencing of both genes, a phenomenon termed cosuppression

  • We analyzed the mRNA and Short interfering RNA (siRNA) of the Chalcone synthase (CHS)-A gene in the white and pigmented portions of petal tissues of petunia plants that have cosuppression or naturally occurring RNA silencing of the chalcone synthase-A (CHS-A) gene

  • Small RNA profiles suggest a common mechanism of RNA degradation in cosuppression and naturally occurring RNA silencing of the CHS-A gene We found that various features of small RNA production in white petal tissues are common to J-type and Red Star plants: predominant size class, exon-2-specific production, the highly abundant species, and in-phase production of siRNAs

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Summary

Introduction

Introduction of a transgene that transcribes RNA homologous to an endogenous gene in the plant genome can induce silencing of both genes, a phenomenon termed cosuppression. The mechanism by which white sectors are generated in nontransgenic petunia is known to be due to RNA silencing of the CHS-A gene as in cosuppression, whether the same trigger(s) and/or pattern of RNA degradation are involved in these phenomena has not been known We addressed this question using deep-sequencing and bioinformatic analyses of small RNAs. RNA silencing refers collectively to diverse RNA-mediated pathways of nucleotide-sequence-specific inhibition of gene expression. In Arabidopsis, small RNA-mediated cleavage can trigger conversion of the targeted RNA to dsRNA by RNA-dependent RNA polymerase 6 (RDR6), which is cleaved into 21-nt phased siRNAs by DCL4 These siRNAs can include those termed transacting siRNAs (tasiRNAs), which silence other gene(s) in trans [10,11,12]. A recent study indicated that the presence of 22-nt RNA in either strand of the small RNA duplex is sufficient for this reaction [15]

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