DNA Methylation Influences the Expression of DICER-LIKE4 Isoforms, Which Encode Proteins of Alternative Localization and Function

• Published in: The Plant cell Vol. 28; no. 11; pp. 2786 - 2804
• Main Authors: Pumplin, Nathan, Sarazin, Alexis, Jullien, Pauline E., Bologna, Nicolas G., Oberlin, Stefan, Voinnet, Olivier
• Format: Journal Article
• Language: English
• Published: United States American Society of Plant Biologists 01-11-2016
• Subjects: Arabidopsis; Arabidopsis - genetics; Arabidopsis - metabolism; Arabidopsis Proteins - genetics; Arabidopsis Proteins - metabolism; Arabidopsis thaliana; DNA Methylation; DNA Transposable Elements - genetics; Gene Expression Regulation, Plant; Protein Isoforms - genetics; Protein Isoforms - metabolism; Ribonuclease III - genetics; RNA Replicase - genetics; RNA Replicase - metabolism; RNA, Small Interfering - genetics
• ISSN: 1040-4651; 1532-298X
• DOI: 10.1105/tpc.16.00554

Plant RNA silencing operates via RNA-directed DNA-methylation (RdDM) to repress transcription or by targeting mRNAs via posttranscriptional gene silencing (PTGS). These pathways rely on distinct Dicer-like (DCL) proteins that process doublestranded RNA (dsRNA) into small-interfering RNAs (siRNAs). Here, we explored the expression and subcellular localization of Arabidopsis thaliana DCL4. DCL4 expression predominates as a transcription start site isoform encoding a cytoplasmic protein, which also represents the ancestral form in plants. A longer DCL4 transcript isoform encoding a nuclear localization signal, DCL4NLS, is present in Arabidopsis, but DNA methylation normally suppresses its expression. Hypomethylation caused by mutation, developmental reprogramming, and biotic stress correlates with enhanced DCL4NLS expression, while hypermethylation of a DCL4 transgene causes a reduction in DCL4NLS expression. DCL4NLS functions in a noncanonical siRNA pathway, producing a unique set of 21-nucleotide-long “disiRNAs,” for DCL4NLS isoform-dependent siRNAs, through the nuclear RdDM dsRNA synthesis pathway. disiRNAs originate mostly from transposable elements (TEs) and TEoverlapping/proximal genes, load into the PTGS effector ARGONAUTE1 (AGO1), and display a subtle effect on transcript accumulation together with overlapping 24-nucleotide siRNAs. We propose that, via PTGS, disiRNAs could help to tighten the expression of epigenetically activated TEs and genes using the methylation-state-responsive DCL4NLS.