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整合 mRNA、microRNA 转录组和降解组分析为毛竹雄蕊发育提供了新的见解。

Integrated mRNA, MicroRNA Transcriptome and Degradome Analyses Provide Insights into Stamen Development in Moso Bamboo.

机构信息

International Center for Bamboo and Rattan, Key Laboratory of Bamboo and Rattan Science and Technology, State Forestry and Grassland Administration, Beijing 100102, China.

Beijing Advanced Innovation Center for Tree Breeding by Molecular Design, Beijing University of Agriculture, Beijing, China.

出版信息

Plant Cell Physiol. 2020 Jan 1;61(1):76-87. doi: 10.1093/pcp/pcz179.

Abstract

A flower is an essential organ for sexual reproduction in flowering plants, which has been extensively studied in model plants. In this study, we used transcriptomic, small RNA and degradome analyses to characterize key microRNAs (miRNAs) and their targets in floral organs of moso bamboo. In total, we identified 13,051 differentially expressed genes and 109 known miRNAs from 26 miRNA families. We aligned the miRNAs to known miRNA databases and revealed some conserved as well as novel miRNAs. Sixteen conserved miRNAs were specifically and highly expressed in stamens, including miRNA159 and miRNA166. In situ hybridization shows that miRNA159 plays a key role in the regulation of stamen development, and the expression levels of its targets PheMYB98 and PheMYB42 were low. Furthermore, Phe-MIRNA159 partially recovers phenotypes of mir159ab double mutant. Overexpression of Phe-MIR159 could cause failure in anther dehisce, and the mature pollens could not be dispersed and further reduce fertility in Arabidopsis. Semi-thin section result shows that anther endothelial layer of Phe-MIRNA159 overexpressing lines is lack of secondary thickening, resulting in limited force for anther opening. Phe-miR159 may regulate the expression of genes related to secondary thickening through negative regulation of AtMYB33, affecting the anther dehiscence. Taken together, this study provides insights regarding molecular networks underlying floral organs development of moso bamboo.

摘要

花是开花植物有性繁殖的重要器官,在模式植物中已得到广泛研究。在这项研究中,我们使用转录组学、小 RNA 和降解组分析来描述毛竹花器官中的关键 microRNAs(miRNAs)及其靶标。总共从 26 个 miRNA 家族中鉴定出 13051 个差异表达基因和 109 个已知 miRNA。我们将 miRNA 与已知的 miRNA 数据库进行比对,揭示了一些保守和新的 miRNA。16 个保守 miRNA 在雄蕊中特异性高度表达,包括 miRNA159 和 miRNA166。原位杂交显示 miRNA159 在雄蕊发育调控中起关键作用,其靶基因 PheMYB98 和 PheMYB42 的表达水平较低。此外,Phe-MIRNA159 部分恢复了 mir159ab 双突变体的表型。Phe-MIR159 的过表达会导致花药开裂失败,成熟花粉无法分散,进一步降低拟南芥的育性。半薄切片结果表明,Phe-MIRNA159 过表达系的花药内皮层缺乏二次加厚,导致花药开口的力有限。Phe-miR159 可能通过负调控 AtMYB33 来调节与次生加厚相关基因的表达,从而影响花药开裂。总之,这项研究为毛竹花器官发育的分子网络提供了新的见解。

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