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植物研究 ›› 2020, Vol. 40 ›› Issue (2): 284-292.doi: 10.7525/j.issn.1673-5102.2020.02.016

• 研究报告 • 上一篇    下一篇

杜仲雄花芽2个发育时期转录组分析

朱利利1,2, 杜庆鑫1,2, 何凤1,2, 庆军1,2, 杜红岩1,2   

  1. 1. 中国林业科学研究院经济林研究开发中心, 郑州 450003;
    2. 国家林业局杜仲工程技术研究中心, 郑州 450003
  • 收稿日期:2019-03-18 出版日期:2020-03-05 发布日期:2020-03-06
  • 通讯作者: 杜红岩,E-maile:dhy515@126.com E-mail:杜红岩,E-maile:dhy515@126.com
  • 作者简介:朱利利(1990-),女,博士研究生,主要从事杜仲育种与栽培。
  • 基金资助:
    "十三五"国家重点研发计划(2017YFD0600702)

Sequencing Analysis of Transcriptome of Male Floral Bud at Two Development Stages in Eucommia ulmoides

ZHU Li-Li1,2, DU Qing-Xin1,2, HE Feng1,2, QING Jun1,2, DU Hong-Yan1,2   

  1. 1. Non-timber Forest Research and Development Center of Chinese Academy of Forestry, Zhengzhou 450003;
    2. Eucommia Engineering Research Center of National Forestry Administration, Zhengzhou 450003
  • Received:2019-03-18 Online:2020-03-05 Published:2020-03-06
  • Supported by:
    The National Key Research and Invention Program of Thirteenth(2017YFD0600702)

摘要: 杜仲(Eucommia ulmoides)雄花富含多种活性成分和营养成分,具有重要的药用和营养价值。为了揭示杜仲雄蕊原基发育相关基因的表达情况,为杜仲雄花芽发育分子调控机制研究提供理论参考。本文以杜仲良种"华仲11号"( "Huazhong No.11" )为材料,采用lllumina高通量测序技术,分别对苞叶原基分化期和雄蕊原基分化期的花芽进行转录组测序,通过生物信息学对2个发育时期的转录组进行比较分析,筛选出与雄花芽形态发育相关的差异基因。结果显示,转录组测序共获得40.48 Gb过滤数据,各样品的clean reads与杜仲基因组进行序列比对,比对效率为90.56%~93.01%。在2个发育时期筛选出583个差异表达基因,其中在雄蕊原基发育期上调基因315个,下调基因267个。差异基因GO和KEGG功能分析显示,差异基因富集在与生长发育、光周期途径、激素合成和信号传导、碳代谢等相关的生物过程和代谢通路。结果显示光周期途径是杜仲成花诱导的重要途径,同时雄花芽在形态分化过程中受碳水化合物、植物激素和其他代谢物质调控。此外,MADS-box家族成员FLCSOC1、AGL3和AGL8参与杜仲雄蕊器官发育。本研究为杜仲花发育基因调控提供了基础数据,也为雄花用杜仲的分子育种提供了参考。

关键词: 杜仲, 雄花芽, 不同发育时期, 转录组测序, 差异表达基因

Abstract: The male floral bud Eucommia ulmoides is rich in healthily kinds of nutrition compositions and active matter, which with a high nutritional and medicinal value. The transcriptome of male floral bud during two differentiation stages was sequenced, aimed to comprehend the expression of genes involved in the stamen development of E.ulcommia. lllumina high-throughput sequencing technology was applied to detect the transcriptome sequencing data of the male flora bud of ‘Huazhong No.11’ during bract differentiation and stamen differentiation stages. Obtained clean data was analyzed including gene function annotation and differentially expressed genes(DEGs) screening was analyzed by bioinformatics methods. A total of 40.48 Gb clean data were obtained, approximately 90.00% of the clean reads were mapped to the E.ulmoides reference genome. It was found that 315 genes were significantly up-regulated and 269 genes were significantly down-regulated in the male flower buds at stamen differentiation stage. GO and KEGG analyses of DEGs showed the DEGs were enriched in development process, photoperiodism, hormone biosynthetic and signal transduction process, carbon metabolism and other processes and pathways associated with flower induction. The photoperiodic was perhaps the most important pathway for the floral induction of E.ulcommia, and the carbohydrates, plant hormone and other metabolic substances was required in the process of male floral bud differentiation. Importantly, the members of MADs-box including FLC, SOC1, AGL3 and AGL8 regulated the stamen formation of E.ulcommia. It provides a significant reference for studying the genes involved in the floral organs and molecular breeding of E.ulcommia.

Key words: Eucommia ulmoides, male floral bud, different developmental stages, transcriptome, differentially expressed genes

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