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中国农学通报 ›› 2019, Vol. 35 ›› Issue (5): 49-57.doi: 10.11924/j.issn.1000-6850.casb18100007

• 林学 园艺 园林 • 上一篇    下一篇

香蕉冷胁迫相关microRNA差异表达分析

王静毅, 刘菊华, 金志强, 徐碧玉   

  1. 中国热带农业科学院热带作物生物技术研究所农业部热带作物生物学与遗传资源利用重点实验室
  • 收稿日期:2018-10-06 修回日期:2018-11-15 接受日期:2018-11-26 出版日期:2019-02-13 发布日期:2019-02-13
  • 通讯作者: 徐碧玉
  • 基金资助:
    国家自然科学基金“香蕉低温胁迫响应miRNA特异表达谱及其靶基因筛选鉴定”(31501043);国家现代农业产业技术体系“国家香蕉产业 技术体系”(CARS-31);中央级公益性科研院所基本科研业务费项目“香蕉基因组学及重要功能基因的挖掘”(1630052017018);中央级公益性科研院 所基本科研业务费项目“香蕉果实品质形成机理及调控技术”(1630052016006)。

Expression Profiling of Cold-responsive MicroRNA in Banana

  • Received:2018-10-06 Revised:2018-11-15 Accepted:2018-11-26 Online:2019-02-13 Published:2019-02-13

摘要: 研究香蕉miRNA在冷胁迫处理下的动态表达,初步探索miRNA在香蕉冷胁迫过程中的可能作用。利用茎环引物实时荧光RT-PCR (stem-loop qRT-PCR)策略,检测冷胁迫响应miRNA在5℃冷胁迫处理不同时间点香蕉幼苗叶片中的表达模式。结果表明,在检测的15个香蕉miRNAs中,不同的miRNA 在同一冷胁迫时间下的表达量存在很大差异。根据其表达模式,可将15个miRNA分成4组。组1 和组2中的12个miRNA (miR159e, miR159f, miR160-3p, miR397a, miR399j, miR164e, miR444a, miR408, miR5179, miR530, miR535和miR5538),在5°C冷胁迫处理下表达量总体为上调,其在胁迫过程中的平均表达水平高于对照CK (0 h) ,说明冷胁迫诱导此类miRNA的表达。第3组包括miR156l、miR162a和miR166a,其在5℃冷胁迫处理各时间点的表达量均低于对照,为下调表达,说明冷胁迫抑制此类miRNA的表达。第4组仅含一个miRNA,即miR156a,除在冷胁迫处理12 h表达量明显上调外,其余时间点均下调表达。对这些miRNAs 作用的靶基因进行预测和分析发现,它们主要参与植物的新陈代谢、信号传导和生长发育过程等。这为进一步验证与低温胁迫相关的目的miRNA 的功能提供理论依据。

关键词: 高温胁迫, 高温胁迫, 油用向日葵, 关键温度, 河套地区

Abstract: To explore the potential roles of miRNA in banana under cold stress, weSanalyzed their dynamic expression of cold responsive miRNAs in banana. The expression profiling of cold-responsive miRNAs in banana leaves was detected by stem-loop qRT-PCR after 0, 2, 4, 8 , 12 and 24 h of cold stress at 5°C. The results showed that fifteen potential cold-responsive miRNA were expressed and exhibited different expression patterns at different treatment stages. The 15 miRNA were divided into four groups according to their expression pattern. Generally, the expressions of Group I (miR159e, miR159f, miR160-3p, miR397a, miR399j, miR408, miR5179, miR530, miR535 and miR5538) and II (miR164e and miR444a) were upregulated at 5°C cold stress. During the cold stress, the average expression level of these miRNA was higher than the control (0 h). miR156l, miR162a and miR166a were in Group III, and their expression was reduced during the whole period of the cold treatment. Group IV had only one miRNA (miR156a). Its expression was significantly increased only at 12 h and reduced at the rest of the time points under cold stress. The analysis on the target genes of these miRNA revealed that these miRNA participated in the signal transduction, growth and development and stress response under abiotic stress. These findings provide valuable information for further functional characterization of miRNA associated with cold stress in banana.

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