Chengdu Institute of Biology, Chinese Academy of Sciences, No.9, Section 4 of South RenMin Road, Wuhou District, Chengdu, 610041, Sichuan, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Funct Integr Genomics. 2020 Mar;20(2):177-190. doi: 10.1007/s10142-019-00710-2. Epub 2019 Aug 21.
MicroRNAs (miRNAs) participate in multiple biological processes in plant. Cd accumulation ability differs among varieties in wheat, but little is known about miRNAs and their function in Cd accumulation of wheat under Cd stress. Therefore, the present study detected small RNAs responsible for differential Cd accumulation between two contrasting wheat genotypes (low-Cd accumulation one L17 and high-Cd accumulation one H17) to identify novel targets to further study Cd stress in wheat. Under normal conditions, 139 miRNAs were differentially expressed between L17 and H17, while this value reached 142 after Cd exposure. For Cd-induced DEMs, total 25 miRNAs were differentially expressed in L17 after Cd treatment, while, 70 Cd-induced DEMs were found in H17. Moreover, GO analysis revealed that target genes of DEMs related to lipid biosynthetic process and chlorophyll binding are uniquely enriched in L17, target genes of DEMs related to ribosome biogenesis and sucrose alpha-glucosidase activity are uniquely enriched in H17. By pathway analysis, target genes of DEMs related to PI3K-Akt signaling pathway was specifically enriched in L17, target genes of DEMs related to carbohydrate digestion and absorption pathway was uniquely enriched in H17. In addition, miRNA-gene co-expression showed that tae-miR9774 was uniquely expressed between L17Cd and L17CK, while tae-miR398 was specially expressed between H17Cd and H17CK. Our results suggested that Cd-accumulating ability of L17 and H17 varied from the expression of induced unique miRNA, such as expression of tae-miR-9774 and tae-miR-398. Our study not only provide the foundation for further exploring the miRNAs-induced molecular mechanisms of Cd accumulation in wheat but also supply novel strategies for improving phytoremediation ability of food plants through genetic engineering.
微小 RNA(miRNAs)参与植物的多种生物学过程。在小麦中,不同品种对镉的积累能力存在差异,但对镉胁迫下小麦中 miRNAs 及其功能知之甚少。因此,本研究检测了两种不同镉积累能力的小麦基因型(低镉积累基因型 L17 和高镉积累基因型 H17)之间差异镉积累的小 RNA,以鉴定新的靶标,进一步研究小麦中的镉胁迫。在正常条件下,L17 和 H17 之间有 139 个 miRNAs 表达差异,而在镉暴露后,这一数值达到了 142 个。对于 Cd 诱导的 DEMs,Cd 处理后 L17 中有 25 个 miRNA 表达差异,而 H17 中有 70 个 Cd 诱导的 DEMs。此外,GO 分析表明,DEMs 靶基因与脂质生物合成过程和叶绿素结合相关的在 L17 中特异富集,与核糖体生物发生和蔗糖α-葡萄糖苷酶活性相关的 DEMs 靶基因在 H17 中特异富集。通过通路分析,DEMs 靶基因与 PI3K-Akt 信号通路相关的在 L17 中特异富集,DEMs 靶基因与碳水化合物消化和吸收途径相关的在 H17 中特异富集。此外,miRNA-基因共表达表明,tae-miR9774 仅在 L17Cd 和 L17CK 之间表达,而 tae-miR398 仅在 H17Cd 和 H17CK 之间表达。我们的结果表明,L17 和 H17 的镉积累能力的差异源于诱导型特异 miRNA 的表达,如 tae-miR-9774 和 tae-miR-398 的表达。本研究不仅为进一步探索小麦中 Cd 积累的 miRNA 诱导分子机制提供了基础,也为通过遗传工程提高食用植物的植物修复能力提供了新的策略。