Affiliation:
1. Institute of Plant Biology and Department of Life Science National Taiwan University Taipei Taiwan
2. Institute of Plant and Microbial Biology Academia Sinica Taipei Taiwan
3. Department of Civil and Environmental Engineering, South Kensington Campus Imperial College London London UK
4. Institute of Molecular Biology National Chung Hsing University Taichung Taiwan
Abstract
AbstractField‐grown rice (Oryza sativa L.), when exposed to various environmental stresses, produces high amounts of reactive oxygen species, such as H2O2. MicroRNAs (miRNAs) play crucial roles in plant stress responses. This study characterized the functions of H2O2‐regulated miRNAs in rice. Small RNA deep sequencing revealed that miR156 levels decreased following H2O2 treatment. Searches of the rice transcriptome and degradome databases indicated that OsSPL2 and OsTIFY11b are miR156‐target genes. Interactions between miR156 and OsSPL2 and OsTIFY11b were confirmed using transient expression assays through agroinfiltration. In addition, the levels of OsSPL2 and OsTIFY11b transcripts were lower in transgenic rice plants overexpressing miR156 than in wild‐type plants. The OsSPL2‐GFP and OsTIFY11b‐GFP proteins were localized to the nucleus. Yeast two‐hybrid and bimolecular fluorescence complementation assays indicated interactions between OsSPL2 and OsTIFY11b. Furthermore, OsTIFY11b interacted with OsMYC2 to regulate the expression of OsRBBI3‐3, which encodes a proteinase inhibitor. The results suggested that H2O2 accumulation in rice suppresses the expression of miR156, and induces the expression of its target genes, OsSPL2 and OsTIFY11b, whose proteins interact in the nucleus to regulate the expression of OsRBBI3‐3, which is involved in plant defense.
Funder
National Taiwan University
Cited by
2 articles.
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