The miR9863 family regulates distinct Mla alleles in barley to attenuate NLR receptor-triggered disease resistance and cell-death signaling

• Published in: PLoS genetics 2014-12, Vol.10 (12), p.e1004755-e1004755
• Main Authors: Liu, Jie, Cheng, Xiliu, Liu, Da, Xu, Weihui, Wise, Roger, Shen, Qian-Hua
• Format: Article
• Language: English
• Subjects: Alleles; Ascomycota; Barley; Base Sequence; Binding sites; Biology and life sciences; Botanical research; Cell Death; Defense; Disease Resistance; Epigenetic Repression; Experiments; Fungi; Gene expression; Gene Expression Regulation, Plant; Gene Silencing; Genetic aspects; Genetic research; Genomes; Health aspects; Hordeum - genetics; Hordeum - microbiology; Infections; MicroRNA; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; Molecular Sequence Data; Nucleic Acid Conformation; Plant Diseases - microbiology; Plant Immunity - genetics; Plant immunology; Plant Proteins - genetics; Plant Proteins - metabolism; Polymorphism, Single Nucleotide; RNA sequencing; RNA, Plant - genetics; RNA, Plant - metabolism; RNA, Small Interfering - genetics; RNA, Small Interfering - metabolism; Signal Transduction; Studies; Transcription, Genetic; Translations; Triticum - genetics
• ISSN: 1553-7404; 1553-7390; 1553-7404
• DOI: 10.1371/journal.pgen.1004755

Barley (Hordeum vulgare L.) Mla alleles encode coiled-coil (CC), nucleotide binding, leucine-rich repeat (NB-LRR) receptors that trigger isolate-specific immune responses against the powdery mildew fungus, Blumeria graminis f. sp. hordei (Bgh). How Mla or NB-LRR genes in grass species are regulated at post-transcriptional level is not clear. The microRNA family, miR9863, comprises four members that differentially regulate distinct Mla alleles in barley. We show that miR9863 members guide the cleavage of Mla1 transcripts in barley, and block or reduce the accumulation of MLA1 protein in the heterologous Nicotiana benthamiana expression system. Regulation specificity is determined by variation in a unique single-nucleotide-polymorphism (SNP) in mature miR9863 family members and two SNPs in the Mla miR9863-binding site that separates these alleles into three groups. Further, we demonstrate that 22-nt miR9863s trigger the biogenesis of 21-nt phased siRNAs (phasiRNAs) and together these sRNAs form a feed-forward regulation network for repressing the expression of group I Mla alleles. Overexpression of miR9863 members specifically attenuates MLA1, but not MLA10-triggered disease resistance and cell-death signaling. We propose a key role of the miR9863 family in dampening immune response signaling triggered by a group of MLA immune receptors in barley.