Genome-wide characterization of the Csa-miR156 family revels its dynamic role in drought stress response in cucumber
摘要
Cucumber (Cucumis sativus L.) production is often compromised by drought stress, resulting in significant yield and quality losses. MicroRNAs (miRNAs) are small non-coding RNAs that play essential roles in regulating plant growth, development, and stress responses. In a previous study, our team obtained miRNA, transcriptome, and degradome sequencing data from drought-stressed cucumber seedlings. Using integrated analyses, we identified 17 members of the miR156 family (Csa-miR156s) and their corresponding target genes in the current study. Bioinformatic approaches were employed to characterize the Csa-miR156s, analyze their expression profiles, and investigate their regulatory relationships with target genes. Additionally, quantitative real-time PCR (qPCR) was used to assess the expression of Csa-miR156s under PEG-simulated drought stress. The results indicated that the miR156 family is divided into four major branches, with the 17 members distributed across them. Fifteen Csa-miR156s were located on five cucumber chromosomes, while the remaining two were repeatedly distributed in chloroplast, mitochondrial, and scaffold sequences. The 17 mature Csa-miR156s were derived from 17 distinct precursor sequences, all of which could form stable stem-loop secondary structures. Analysis of promoter regions revealed that Csa-miR156s contained cis-acting elements associated with responses to light, hormones, or stresses, as well as biosynthesis and metabolism. Expression analyses showed differential expression patterns between Csa-miR156s and their target genes, and qPCR confirmed significant changes in Csa-miR156 expression under drought stress compared with controls. These results suggest that Csa-miR156s are likely involved in the drought stress response in cucumber, thus providing a robust theoretical foundation and offering candidate genes for the future genetic improvement of drought tolerance in cucumber.