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花生AhDGAT2a基因启动子的克隆和功能验证

郑玲 史灵敏 田海莹 单雷 边斐 郭峰 宣宁 万书波 彭振英

作物学报2016,Vol.42Issue(7):1094-1099,6.
作物学报2016,Vol.42Issue(7):1094-1099,6.DOI:10.3724/SP.J.1006.2016.01094

花生AhDGAT2a基因启动子的克隆和功能验证

Cloning and Functional Analysis of PeanutAhDGAT2a Promoter

郑玲 1史灵敏 2田海莹 1单雷 3边斐 1郭峰 2宣宁 1万书波 2彭振英1

作者信息

  • 1. 山东省农业科学院生物技术研究中心 /山东省作物遗传改良与生态生理重点实验室,山东济南 250100
  • 2. 山东大学生命科学学院,山东济南 250100
  • 3. 新疆农业大学农学院,新疆乌鲁木齐 830000
  • 折叠

摘要

Abstract

Diacylglycerol acyltransferase (DGAT) is a rate-limiting enzyme in triacylglycerol (TAG) biosynthesis pathway. In this study, GenomeWalking method was used for cloning the promoter sequence ofAhDGAT2a gene from Luhua 14, and finally a 1200 bp fragment flanking 5′-upstream ofAhDGAT2a was obtained and named as pAhDGAT2a. The crucial regulatory elements in pAhDGAT2a were further analyzed with software PlantCARE. There were many TATA-box, CAAT-box, light regulation, stress and defense response and hormone response elements. To assess the activity of pAhDGAT2a, we constructed pAhDGAT2a:GUS cassettes and introduced it into the tobacco SR1 genome by Agrobacterium-mediated transformation. Expression pattern was monitored by histochemical staining. Results showed that GUS activity driven by the pAhDGAT2a was detected in almost all vegetative and reproductive tissues, with a higher expression level in stigma, anther and young seeds than in the other organs, indicating thatpAhDGAT2a has a constitutive promoter activity.

关键词

花生/AhDGAT2a基因/启动子/功能验证

Key words

Arachis hypogaeaL./AhDGAT2a gene/Promoter/Function analysis

引用本文复制引用

郑玲,史灵敏,田海莹,单雷,边斐,郭峰,宣宁,万书波,彭振英..花生AhDGAT2a基因启动子的克隆和功能验证[J].作物学报,2016,42(7):1094-1099,6.

基金项目

本研究由山东省自然科学基金项目(ZR2013CM036)和山东省良种工程项目(2014-2017)资助。 This study was supported by Natural Science Foundation of Shandong (ZR2013CM036) and Shandong Province Germplasm Innovation and Utilization Project (2014-2017) (ZR2013CM036)

作物学报

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