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A combined microRNA and transcriptome analyses illuminates the resistance response of rice against brown planthopper
A combined microRNA and transcriptome analyses illuminates the resistance response of rice against brown planthopper
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A combined microRNA and transcriptome analyses illuminates the resistance response of rice against brown planthopper
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A combined microRNA and transcriptome analyses illuminates the resistance response of rice against brown planthopper
A combined microRNA and transcriptome analyses illuminates the resistance response of rice against brown planthopper

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A combined microRNA and transcriptome analyses illuminates the resistance response of rice against brown planthopper
A combined microRNA and transcriptome analyses illuminates the resistance response of rice against brown planthopper
Journal Article

A combined microRNA and transcriptome analyses illuminates the resistance response of rice against brown planthopper

2020
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Overview
Background The brown planthopper (BPH, Nilaparvata lugens Stål) is a kind of phloem-feeding pest that adversely affects rice yield. Recently, the BPH-resistance gene, BPH6 , was cloned and applied in rice breeding to effectively control BPH. However, the molecular mechanisms underlying BPH6 are poorly understood. Results Here, an integrated miRNA and mRNA expression profiling analysis was performed on BPH6-transgenic (BPH6G) and Nipponbare (wild type, WT) plants after BPH infestation, and a total of 217 differentially expressed miRNAs (DEMs) and 7874 differentially expressed mRNAs (DEGs) were identified. 29 miRNAs, including members of miR160, miR166 and miR169 family were opposite expressed during early or late feeding stages between the two varieties, whilst 9 miRNAs were specifically expressed in BPH6G plants, suggesting involvement of these miRNAs in BPH6-mediated resistance to BPH. In the transcriptome analysis, 949 DEGs were opposite expressed during early or late feeding stages of the two genotypes, which were enriched in metabolic processes, cellular development, cell wall organization, cellular component movement and hormone transport, and certain primary and secondary metabolite synthesis. 24 genes were further selected as candidates for BPH resistance. Integrated analysis of the DEMs and DEGs showed that 34 miRNAs corresponding to 42 target genes were candidate miRNA-mRNA pairs for BPH resistance, 18 pairs were verified by qRT-PCR, and two pairs were confirmed by in vivo analysis. Conclusions For the first time, we reported integrated small RNA and transcriptome sequencing to illustrate resistance mechanisms against BPH in rice. Our results provide a valuable resource to ascertain changes in BPH-induced miRNA and mRNA expression profiles and enable to comprehend plant-insect interactions and find a way for efficient insect control.