生物技术通报 ›› 2021, Vol. 37 ›› Issue (8): 141-151.doi: 10.13560/j.cnki.biotech.bull.1985.2021-0068

• 研究报告 • 上一篇    下一篇

葡萄AKR基因家族的鉴定和组织特异性表达分析

马亚男1(), 卢旭2, 魏云春1, 李康1, 魏若男1, 李胜1(), 马绍英3()   

  1. 1.甘肃农业大学生命科学技术学院,兰州 730070
    2.甘肃农业大学园艺学院,兰州 730070
    3.甘肃农业大学基础实验教学中心,兰州 730070
  • 收稿日期:2021-01-17 出版日期:2021-08-26 发布日期:2021-09-10
  • 作者简介:马亚男,女,硕士研究生,研究方向:农艺与种业;E-mail: m568518983@qq.com
  • 基金资助:
    甘肃省重大专项(20ZD7NA007-02)

Identification and Tissue Specific Expression Analysis of AKR Gene Family in Grape

MA Ya-nan1(), LU Xu2, WEI Yun-chun1, LI Kang1, WEI Ruo-nan1, LI Sheng1(), MA Shao-ying3()   

  1. 1. College of Life Science and Technology,Gansu Agricultural University,Lanzhou 730070
    2. College of horticulture,Gansu Agricultural University,Lanzhou 730070
    3. Basic Experimental Teaching Center of Gansu Agricultural University,Lanzhou 730070
  • Received:2021-01-17 Published:2021-08-26 Online:2021-09-10

摘要:

醛酮还原酶(aldo-keto reductase,AKR)是一类NADP-依赖型氧化还原酶,通过对葡萄AKR基因鉴定分析,旨在揭示葡萄AKR基因分子生物学功能和遗传调控机制。基于2020年最新组装的葡萄参考基因组数据,利用生物信息学对葡萄AKR基因进行理化性质、基因结构、Motif分析、顺式作用元件、亚细胞定位、二级结构预测以及组织特异性表达分析,最后用荧光定量分析了葡萄AKR基因在盐胁迫下表达水平变化。从全基因组水平上共鉴定出13个葡萄AKR基因家族成员,分为2个亚族;基因结构分析显示,不同成员编码的氨基酸序列外显子数目及位置存在差异;motif分析表明,AKR蛋白保守结构域高度相似;顺式作用元件分析显示,该基因上游启动子元件不仅存在核心元件和增强元件,同时还存在各种激素及胁迫响应元件,器官特异性元件和光调控元件;二级结构和亚细胞定位预测表明,该基因家族主要在细胞核中表达,并以α-螺旋和不规则卷曲为主。基因芯片表达谱分析显示,AKR家族成员间表达水平差异大且存在组织特异性。荧光定量结果显示,盐胁迫条件下VvAKR02、VvAKR05、VvAKR07、VvAKR11、VvAKR12和VvAKR13表达量显著上调。从葡萄中鉴定了13个AKR家族基因,并分析其盐胁迫下的表达水平,对于挖掘葡萄AKR家族中耐盐基因提供了一定的理论依据和实验基础。

关键词: 葡萄, AKR基因家族, 生物信息学, 基因芯片表达谱, 盐胁迫

Abstract:

Aldo-Keto Reductase(AKR)is a kind of NADP-dependent oxidoreductase. Through the identification and analysis of grape AKR genes,the aim is to reveal the molecular biological function and genetic regulation mechanism of AKR genes. Based on the latest assembly reference genome data of grape in 2020,bioinformatics was used to analyze the physicochemical properties,gene structure,Motif analysis,cis-acting elements,subcellular localization,secondary structure prediction,and tissue-specific expression analysis of grape AKR genes. Finally,fluorescence quantitative analysis was used to analyze the change of grape AKR gene expressions under salt stress. Thirteen members of AKR gene family were identified at the genome-wide level and divided into 2 subfamilies. Genetic structure analysis demonstrated that the number and location of exons among different members varied. Motif analysis showed that the conserved domains of AKR protein were highly similar. The cis-acting element analysis showed that the upstream promoter elements of this gene not only had core elements and enhancement elements,but also had various hormone and stress response elements,organ specific elements and light regulatory elements. The prediction of secondary structure and subcellular localization indicated that the gene family was mainly expressed in the nucleus,and was dominated by α-helix and irregular coil. Analysis via gene chip expression profile showed that the expression levels of AKR family members were significantly different and had tissue specificity. Fluorescence quantitative results showed that the expression levels of VvAKR02,VvAKR05,VvAKR07,VvAKR11,VvAKR12 and VvAKR13 were up-regulated under salt stress. In conclusion,13 AKR family genes were identified from grape and their expression levels under salt stress were analyzed,which may provide a theoretical and experimental basis for mining salt-tolerant genes in AKR family of grape.

Key words: grape, the AKR gene family, bioinformatics, gene chip expression profile, salt stress