期刊文献+

北柴胡成花基因的克隆及时空表达分析 被引量:3

Cloning and spatio-temporal expression analysis of flowering genes in Bupleurum chinense DC.
原文传递
导出
摘要 开花是植物生长发育的关键环节,本研究从北柴胡植株中克隆得到4个与成花相关的基因,分别命名为BcSVP、BcPAF1、BcCO、BcFT,并进行了同源性比对;以actin和EF-1α作为双内参,对4个基因在北柴胡植株不同器官和不同发育阶段的时空表达差异进行分析。结果表明,BcSVP主要在根中表达,相对表达量较低;BcPAF1和BcCO在不同部位均有较高表达,二者相对表达量伴随花期进程均呈先上升后缓慢下降趋势;BcFT基因主要在茎中表达,相对表达量在盛花期急剧上升。本文首次克隆并分析了与北柴胡植株成花相关4个基因的相对表达量,为解析柴胡植株成花分子调控机制奠定了基础。 In this study we isolated and cloned four flowering-related genes from Bupleurum chinense DC.,named BcSVP,BcPAF1,BcCO,and BcFT.Actin and EF-1αwere used as double internal standards to analyze the spatial and temporal differences in the expression of four genes in different tissues and flowering stages of Bupleurum chinense DC.qRT-PCR analysis showed that the BcSVP gene was mainly expressed in root,and its relatively expression level was low.BcPAF1 and BcCO were both highly expressed in different parts,and their relative expression level showed an increasing trend and then slowly decreasing with the flowering development process.BcFT was mainly expressed in the stem,and the relatively expression level was increased sharply in the flowering stage.In summary,four genes related to flowering of Bupleurum chinense DC.were cloned and their relative expression levels were characterized,laying a foundation for elucidating the molecular mechanisms that regulate the flowering stage of Bupleurum chinense.
作者 李敏 张全芳 蒲高斌 刘艳艳 刘谦 步迅 张永清 LI Min;ZHANG Quan-fang;PU Gao-bin;LIU Yan-yan;LIU Qian;BU Xun;ZHANG Yong-qing(Shandong University of Traditional Chinese Medicine,Jinan 250355,China;Bio-Tech Research Center,Shandong Academy of Agricultural Sciences,Jinan 250100,China)
出处 《药学学报》 CAS CSCD 北大核心 2021年第4期1188-1196,共9页 Acta Pharmaceutica Sinica
基金 山东省高校中药质量控制与全产业链建设协同创新中心(CYLXTCX2020) 山东省重点研发计划(2019GSF108163) 山东省重点研发计划“中医经方精准化关键技术示范研究”课题(2016CYJS08A01) 山东省创新公共服务平台计划(2018JGX111) 山东省政府公派出国留学项目(201802036)。
关键词 北柴胡 成花基因 克隆 时空表达模式 Bupleurum chinense flowering gene cloning spatio-temporal expression
  • 相关文献

参考文献13

二级参考文献150

共引文献448

同被引文献59

引证文献3

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部