Journal
HORTICULTURE RESEARCH
Volume 9, Issue -, Pages -Publisher
OXFORD UNIV PRESS INC
DOI: 10.1093/hr/uhac192
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Funding
- National Key R&D Program of China [2019YFD1000102-02]
- National Natural Science Foundation of China [31972390]
- Construction of Beijing Science and Technology Innovation and Service Capacity in Top Subjects [CEFF-PXM2019_014207_000032]
- 2115 Talent Development Program of China Agricultural University
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This study reports the identification of drought-responsive miRNA, miR164g, in the wild apple species Malus sieversii and elucidates its role in apple drought tolerance. MiR164g expression is significantly inhibited under drought stress and it cleaves the transcripts of the transcription factor MsNAC022. Overexpression of miR164g enhances sensitivity to drought stress, while overexpression of MsNAC022 increases tolerance to drought stress by enhancing ROS scavenging enzymes activity and related gene expression levels.
Under drought stress, reactive oxygen species (ROS) overaccumulate as a secondary stress that impairs plant performance and thus severely reduces crop yields. The mitigation of ROS levels under drought stress is therefore crucial for drought tolerance. MicroRNAs (miRNAs) are critical regulators of plant development and stress responses. However, the complex molecular regulatory mechanism by which they function during drought stress, especially in drought-triggered ROS scavenging, is not fully understood. Here, we report a newly identified drought-responsive miRNA, miR164g, in the wild apple species Malus sieversii and elucidate its role in apple drought tolerance. Our results showed that expression of miR164g is significantly inhibited under drought stress and it can specifically cleave transcripts of the transcription factor MsNAC022 in M. sieversii. The heterologous accumulation of miR164g in Arabidopsis thaliana results in enhanced sensitivity to drought stress, while overexpression of MsNAC022 in Arabidopsis and the cultivated apple line 'GL-3' (Malus domestica Borkh.) lead to enhanced tolerance to drought stress by raising the ROS scavenging enzymes activity and related genes expression levels, particularly PEROXIDASE (MsPOD). Furthermore, we showed that expression of MsPOD is activated by MsNAC022 in transient assays. Interestingly, Part1 (P1) region is the key region for the positive regulation of MsPOD promoter by MsNAC022, and the different POD expression patterns in M. sieversii and M. domestica is attributed to the specific fragments inserted in P1 region of M. sieversii. Our findings reveal the function of the miR164g-MsNAC022 module in mediating the drought response of M. sieversii and lay a foundation for breeding drought-tolerant apple cultivars.
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