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Integrative physiological evaluation and whole-transcriptome analysis reveal non-coding RNA–associated drought responses in oat (Avena sativa L.)

Sep 2026 · BMC Plant Biology · 0 citations

TL;DR

A comprehensive overview of ncRNA-mediated drought responses in oat seedlings is provided by integrating physiological evaluation with whole-transcriptome profiling, and the predicted regulatory networks provided valuable candidate regulatory modules for future functional validation and molecular breeding aimed at improving drought tolerance in oat.

Abstract

Oat ( Avena sativa L.) is an important cereal crop used for both food and forage production, but its productivity is severely constrained by drought stress. Although non-coding RNAs (ncRNAs) are increasingly recognized as key regulators of plant responses to abiotic stress, the coordinated regulatory roles of long non-coding RNAs (lncRNAs), circular RNAs (circRNAs), and microRNAs (miRNAs) in oat drought adaptation remain poorly understood. In this study, four oat cultivars with contrasting drought tolerance were evaluated at the seedling stage under controlled drought conditions using 21 morphological, physiological, and photosynthetic traits. Principal component analysis (PCA) was performed to calculate a comprehensive drought resistance index ( F value), allowing an integrated assessment of drought tolerance among the cultivars. Zhongyan No.1 (Z1) exhibited the highest drought tolerance, followed by Baiyan No.7 (B7), Denmark 440 (D4), and Longyan No.3 (L3). Based on these results, leaves from Z1 plants exposed to drought for 6 days were selected for whole-transcriptome sequencing. Transcriptome analysis identified 10,446 differentially expressed mRNAs, 116 differentially expressed lncRNAs, and 13 differentially expressed miRNAs. Functional enrichment analyses revealed that these drought-responsive transcripts were significantly enriched in pathways related to photosynthetic carbon fixation, starch and sucrose metabolism, glycolysis/gluconeogenesis, and glyoxylate and dicarboxylate metabolism, suggesting extensive transcriptional reprogramming of carbon metabolism in response to drought stress. Furthermore, an lncRNA–miRNA–mRNA competing endogenous RNA (ceRNA) network was constructed, identifying a drought-responsive regulatory module centered on miR156 and comprising two lncRNAs, one miRNA, and eleven target mRNAs. By integrating physiological evaluation with whole-transcriptome profiling, this study provided a comprehensive overview of ncRNA-mediated drought responses in oat seedlings by integrating physiological evaluation with whole-transcriptome profiling. The predicted regulatory networks, particularly the miR156-centered ceRNA module, provided valuable candidate regulatory modules for future functional validation and molecular breeding aimed at improving drought tolerance in oat.

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