4.8 Article

Osa-miR1320 targets the ERF transcription factor OsERF096 to regulate cold tolerance via JA-mediated signaling

Journal

PLANT PHYSIOLOGY
Volume 189, Issue 4, Pages 2500-2516

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/plphys/kiac208

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Funding

  1. National Natural Science Foundation of China [31971826, U20A2025]
  2. Special Funds from the Central Finance to Support the Development of Local Universities
  3. China Postdoctoral Science Foundation [2021T140185, 2020M670929]
  4. Postdoctoral Science Foundation of Heilongjiang Province [LBH-Z20028]
  5. Fund Program for the Scientific Activities of Selected Returned Overseas Professionals in Heilongjiang Province
  6. Open Project of Key Laboratory of Germplasm Enhancement, Physiology and Ecology of Food Crops in Cold Region
  7. Ministry of Education [CXSTOP2021001]

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miR1320, a rice species-specific microRNA, regulates cold stress tolerance in rice by targeting the ethylene-responsive transcription factor OsERF096 and repressing the JA-mediated cold signaling pathway. The study provides insights into the regulatory mechanism of miR1320 and OsERF096 under cold stress and demonstrates the impact of OsERF096 on hormone content and signaling pathways.
miR1320, a rice species-specific microRNA, targets the ethylene-responsive transcription factor OsERF096 to regulate cold stress tolerance by repressing JA-mediated cold signaling pathway. MicroRNAs play key roles in abiotic stress response. Rice (Oryza sativa L.) miR1320 is a species-specific miRNA that contributes to miR168-regulated immunity. However, it is still unknown whether miR1320 is involved in rice response to abiotic stress. In this study, we illustrated that the miR1320 precursor generated two mature miR1320s, miR1320-3p, and miR1320-5p, and they both displayed decreased expression under cold stress. Genetic evidence showed that miR1320 overexpression resulted in increased cold tolerance, while miR1320 knock down (KD) reduced cold tolerance. Furthermore, an APETALA2/ethylene-responsive factor (ERF) transcription factor OsERF096 was identified as a target of miR1320 via 5 '-RACE and dual luciferase assays. OsERF096 expression was altered by miR1320 overexpression and KD and exhibited an opposite pattern to that of miR1320 in different tissues and under cold stress. Consistently, OsERF096 negatively regulated cold stress tolerance. Furthermore, we suggested that OsERF096 could bind to the GCC and DRE cis-elements and act as a transcriptional activator in the nucleus. Based on RNA-sequencing and targeted metabolomics assays, we found that OsERF096 modified hormone content and signaling pathways. Finally, phenotypic and reverse transcription-quantitative PCR assays showed that jasmonic acid (JA) methyl ester application recovered the cold-sensitive phenotype and JA-activated expression of three Dehydration Responsive Element Binding genes in the OsERF096-OE line. Taken together, our results strongly suggest that the miR1320-OsERF096 module regulates cold tolerance by repressing the JA-mediated cold signaling pathway.

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