梅PmARF17克隆及其在花发育中与内源激素的调控模式  

Isolation of PmARF17 and Its Regulation Pattern of Endogenous Hormones During Flower Development in Prunus mume

作　　者：李艳林 SHAHID Iqbal 侍婷[1] 宋娟 倪照君[1] 高志红[1] LI YanLin;SHAHID Iqbal;SHI Ting;SONG Juan;NI ZhaoJun;GAO ZhiHong(College of Horticulture,Nanjing Agricultural University,Nanjing 210095;Jiangsu Academy of Agricultural Sciences,Nanjing 210014)

机构地区：[1]南京农业大学园艺学院,南京210095 [2]江苏省农业科学院,南京210014

出　　处：《中国农业科学》2021年第13期2843-2857,共15页Scientia Agricultura Sinica

基　　金：国家自然科学基金(31971703,31772282);中国博士后基金(2018M640497);江苏省博士后基金(2018K216C);中央高校基本科研业务费专项资金(SYSB201805)。

摘　　要：【目的】分析梅PmARF17的生物学功能,探究梅花发育进程中其表达丰度与内源激素动态变化的关系,为梅花发育的调控研究提供依据。【方法】以梅品种‘大嵌蒂’为试材,克隆PmARF17,利用生物信息学软件分析基因结构、系统进化及其与其他物种同源蛋白的差异;亚细胞定位确定PmARF17蛋白在细胞中作用的部位;以梅品种‘大嵌蒂’和‘龙眼’不同发育阶段的花芽、叶芽、花器官为试材,利用qRT-PCR检测PmARF17时空表达模式,通过UPLC法测定IAA、GA3、ABA、ZT含量的动态变化,并与PmARF17的表达进行相关性分析;克隆PmARF17启动子,分析启动子的顺式作用元件,利用瞬时表达解析PmARF17与GA3的调控模式。【结果】从梅品种‘大嵌蒂’中克隆得到PmARF17,系统进化树分析表明PmARF17蛋白与其他植物的ARF蛋白序列高度同源;亚细胞定位表明其作用于细胞核和细胞膜上;qRT-PCR表达和内源激素含量的相关性分析表明,PmARF17的表达与IAA含量的变化趋势没有明显的相关性。PmARF17在雌蕊完好花芽中的表达水平相对不完全花芽显著上调,而GA3含量与PmARF17的表达趋势一致。ABA和ZT含量总体上与PmARF17的表达呈相反的趋势,表明两者可能抑制PmARF17的表达。PmARF17启动子含有GA顺式元件,且具有启动活性和组织表达特异性,在花瓣、雄蕊及根部特异表达。【结论】PmARF17可能是梅花发育的正调控基因,促进梅雌蕊的正常发育。PmARF17的表达可能受到GA3的正调控,其可能通过作用于雄蕊和花瓣,进而影响梅的雌蕊发育进程。【Objective】The purposes of this study were to analyze the biological functions of PmARF17 gene and to explore the regulation pattern between the expression of PmARF17 and plant endogenous hormones,which could provide the basis for studying the regulatory mechanism of pistil abortion in Prunus mume.【Method】PmARF17 gene was isolated from the cultivar Daqiandi of Prunus mume,and the gene structure,phylogeny and homology with other species were analyzed by bioinformatics software.Subcellular localization determined the position of PmARF17 protein in the cell.qRT-PCR was used to detect the spatiotemporal expression pattern of PmARF17 in different stages of flower buds,leaf buds,flower buds with different pistil morphology,and different mature floral organs of the varieties Daqiandi and Longyan.The contents of IAA,GA3,ABA and ZT in flower buds,leaf buds,pistil morphology flower buds and different mature flower organs of Daqiandi and Longyan were determined by UPLC method,and the correlation analysis was conducted with the q RT-PCR expression of PmARF17.Cloning,element analysis and transient expression of Pm ARF17 promoter were performed to study the regulation pattern between PmARF17 and GA3.【Result】Phylogenetic tree analysis showed PmARF17 protein sequence was highly conserved with ARF protein of other plants.Subcellular localization experiment showed PmARF17 protein was located on the nucleus and cell membrane.The correlation analysis between q RT-PCR expression and endogenous hormone content showed the expression of PmARF17 had no obvious similarity with the change trend of IAA content in different flower samples.The expression of PmARF17 in complete pistil was significantly up-regulated compared to incomplete pistil,and GA3 content was consistent with the expression trend of PmARF17.The content of ABA and ZT in different flower samples and the expression of PmARF17 showed an overall opposite trend,indicating that they might inhibit the expression of Pm ARF17.The Pm ARF17 promoter contained GA cis-elemen

关 键 词：梅 生长素响应因子 雌蕊发育 基因表达 内源激素 瞬时表达 

分 类 号：S662.4[农业科学—果树学]