华北农学报 ›› 2019, Vol. 34 ›› Issue (5): 23-29. doi: 10.7668/hbnxb.201751719

所属专题: 生物技术

• 作物遗传育种·种质资源·生物技术 • 上一篇    下一篇

菘蓝IiCYP79B2基因的克隆与表达分析

胡向阳, 屈新运, 吴格格, 秦苗苗, 刘蕊, 高天娥, 李焘   

  1. 西北濒危药材资源开发国家工程实验室, 药用资源与天然药物化学教育部重点实验室, 陕西师范大学, 陕西 西安 710119
  • 收稿日期:2019-04-06 出版日期:2019-10-28
  • 通讯作者: 李焘(1976-),女,湖南衡阳人,副教授,博士,主要从事植物次生代谢调控研究。
  • 作者简介:胡向阳(1994-),男,河南驻马店人,硕士,主要从事植物次生代谢调控研究。
  • 基金资助:
    国家重点研发计划中医药现代化研究重点专项(2017YFC1701300);陕西省社会发展科技攻关项目(2016SF-390);陕西师范大学勤助科研项目(KY2018YB004)

Cloning and Expression Analysis of IiCYP79B2 from Isatis indigotica Fort.

HU Xiangyang, QU Xinyun, WU Gege, QIN Miaomiao, LIU Rui, GAO Tian, LI Tao   

  1. National Engineering Laboratory for Resource Developing of Endangered Chinese Crude Drugs in Northwest of China, Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, Shaanxi Normal University, Xi'an 710119, China
  • Received:2019-04-06 Published:2019-10-28

摘要: 为了探究菘蓝IiCYP79B2基因的结构、特性和功能,对菘蓝IiCYP79B2基因进行了克隆,并进一步开展了生物信息学分析和不同条件下的表达模式研究。相关研究结果显示:IiCYP79B2基因全长1 827 bp,包含1个内含子,ORF全长1 629 bp,编码542个氨基酸。其编码的蛋白含有2个跨膜结构域,无信号肽,定位于叶绿体类囊体膜上,属于主要由无规则卷曲和α-螺旋构成的亲水性蛋白,与白芥的亲缘关系最近。qRT-PCR分析结果表明:IiCYP79B2基因在菘蓝各组织中的表达量由高到低依次为叶 > 茎 > 果 > 花 > 根,在不同发育时期的表达量依次为营养生长期 > 花期 > 幼苗期 > 萌芽期;此外,该基因的表达还显著响应茉莉酸甲酯(MJ)和葡萄糖(Glu)信号的诱导,受到水杨酸(SA)和低温(Cold)胁迫的抑制。相关研究结果为进一步探讨IiCYP79B2基因的功能提供了有效的试验依据。

关键词: 菘蓝, IiCYP79B2, 基因克隆, 表达分析

Abstract: In order to explore the structure, characteristics and functions of IiCYP79B2 gene in Isatis indigotica, the IiCYP79B2 gene was cloned and the bioinformatics analysis and expression patterns under different conditions were carried out. The results showed that the full length of the gene was 1 827 bp with an intron, and its ORF was 1 629 bp, encoding 542 amino acids. IiCYP79B2 protein contained two transmembrane domains without signal peptide. The protein was localized in the chloroplast thylakoid membrane and mainly consisted of random coils and α-helix structures, having the closest relationship with Sinapis alba. The qRT-PCR analysis showed that the expression levels of IiCYP79B2 in different tissues were leaf > stem > fruit > flower > root, and the expression levels at different development stages were vegetative growth > flowering > seedling > germination. Moreover, IiCYP79B2 could be induced significantly by MJ and Glu, and repressed by SA and cold. The obtained results provided some experimental evidences for further studying the functions of IiCYP79B2 gene.

Key words: Isatis indigotica Fort., IiCYP79B2, Gene cloning, Expression analysis

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引用本文

胡向阳, 屈新运, 吴格格, 秦苗苗, 刘蕊, 高天娥, 李焘. 菘蓝IiCYP79B2基因的克隆与表达分析[J]. 华北农学报, 2019, 34(5): 23-29. doi: 10.7668/hbnxb.201751719.

HU Xiangyang, QU Xinyun, WU Gege, QIN Miaomiao, LIU Rui, GAO Tian, LI Tao. Cloning and Expression Analysis of IiCYP79B2 from Isatis indigotica Fort.[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2019, 34(5): 23-29. doi: 10.7668/hbnxb.201751719.

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