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杜鹃红山茶CaAPX基因的克隆、表达及功能分析
引用本文:王江英,范正琪,殷恒福,李辛雷,吴斌,李纪元. 杜鹃红山茶CaAPX基因的克隆、表达及功能分析[J]. 林业科学研究, 2016, 29(4): 471-479
作者姓名:王江英  范正琪  殷恒福  李辛雷  吴斌  李纪元
作者单位:中国林业科学研究院亚热带林业研究所, 浙江省林木育种技术研究重点实验室, 浙江 杭州 311400;江苏省连云港市农业科学院花卉研究中心, 江苏 连云港 222006;中国林业科学研究院亚热带林业研究所, 浙江省林木育种技术研究重点实验室, 浙江 杭州 311400;中国林业科学研究院亚热带林业研究所, 浙江省林木育种技术研究重点实验室, 浙江 杭州 311400;中国林业科学研究院亚热带林业研究所, 浙江省林木育种技术研究重点实验室, 浙江 杭州 311400;中国林业科学研究院亚热带林业研究所, 浙江省林木育种技术研究重点实验室, 浙江 杭州 311400;中国林业科学研究院亚热带林业研究所, 浙江省林木育种技术研究重点实验室, 浙江 杭州 311400
基金项目:国家‘十二·五’科技支撑计划课题(2012BAD01B0703);浙江省花卉新品种选育重大科技专项(2012C12909-6);浙江省与中国林业科学研究院省院合作林业科技项目(2012SY02);国家农业科技成果转化资金项目(GB2013GB24320606);国家林业局引进国际先进林业科学技术项目(948项目)(2014-4-16)
摘    要:[目的]利用分子生物学技术探讨杜鹃红山茶CaAPX基因的表达模式及在模式植物烟草中所起的抗寒、耐热作用,为今后山茶花抗逆育种奠定基础。[方法]根据山茶花同源序列设计特异性引物,利用同源克隆和3’,5’-RACE技术,从杜鹃红山茶嫩叶组织中克隆出抗坏血酸过氧化物酶(APX),命名为CaAPX,基因全长1 097 bp,开放阅读框753 bp,编码250个氨基酸。实时荧光定量PCR对杜鹃红山茶7种组织和温度胁迫下该基因的表达模式进行分析。[结果]表明:CaAPX基因在杜鹃红山茶7种组织中均得到表达,但表达水平不一,表达量由高到低依次为:未成熟果实嫩叶花苞叶芽种胚花瓣花芽,其中,未成熟果实中的表达量是其它组织的2.6811.44倍;温度胁迫处理8 h后该基因呈上调表达,CaAPX基因表达量分别是0 h的3.49和2.67倍。CaAPX基因转化烟草分析表明,过量表达CaAPX基因后,APX活性提高了2.58 4.09倍,抗坏血酸(As A)含量提高了2.673.56倍,并且转基因烟草植株的抗寒、耐热能力也获得提高。[结论]通过过量表达CaAPX基因能够提高烟草植株的抗寒、耐热性,为山茶花抗逆育种提供了科学依据。

关 键 词:杜鹃红山茶  基因克隆  温度胁迫  表达分析  转基因烟草
收稿时间:2015-05-12

Cloning, Expression and Functional Analysis of CaAPX Gene from Camellia azalea
WANG Jiang-ying,FAN Zheng-qi,YIN Heng-fu,LI Xin-lei,WU Bin and LI Ji-yuan. Cloning, Expression and Functional Analysis of CaAPX Gene from Camellia azalea[J]. Forest Research, 2016, 29(4): 471-479
Authors:WANG Jiang-ying  FAN Zheng-qi  YIN Heng-fu  LI Xin-lei  WU Bin  LI Ji-yuan
Affiliation:Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Key Laboratory of Tree Breeding of Zhejiang Province, Hangzhou 311400, Zhejiang, China;Flower Research Center of Lianyungang Academy of Agricultural Sciences, Lianyungang 222006, Jiangsu, China;Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Key Laboratory of Tree Breeding of Zhejiang Province, Hangzhou 311400, Zhejiang, China;Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Key Laboratory of Tree Breeding of Zhejiang Province, Hangzhou 311400, Zhejiang, China;Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Key Laboratory of Tree Breeding of Zhejiang Province, Hangzhou 311400, Zhejiang, China;Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Key Laboratory of Tree Breeding of Zhejiang Province, Hangzhou 311400, Zhejiang, China;Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Key Laboratory of Tree Breeding of Zhejiang Province, Hangzhou 311400, Zhejiang, China
Abstract:[Objective] Using molecular biology techniques to investigate the expression patterns of CaAPX gene in Camellia azalea, and to carry out the functional analysis of CaAPX in tobacco under temperature stress. [Method] On the basis of homologous sequences of C. japonica, an ascorbate peroxidase (APX) gene was isolated from the tender leaf in C. azalea by the 3'', 5''-RACE technology named CaAPX. The full-length cDNA of CaAPX is 1 097 bp, containing a 753 bp ORF which encodes 250 amino acids. [Result] Quantitative real-time PCR analysis indicated that the CaAPX was expressed differently in all examined camellia tissues, and the expression levels in order were immature green fruit, tender leaf, flower, leaf bud, seed embryo, petal and flower bud. The highest expression level of CaAPX was in immature green fruit, approximately ranging 2.68 to 11.44 times as high as that of the other six groups. It was also found that the expression level was notably up-regulated in leaves of camellia plants subjected to abnormal temperatures. Furthermore, the APX activity in transgenic plants increased by 158%-309%, and the AsA content increased by 167%-256% as higher as wild type plants. In addition, the over expression of CaAPX enhanced cold and heat stress tolerance in transgenic plants under temperature stresses. [Conclusion] The over expression of CaAPX from C. azalea could enhance the cold and heat stress tolerance in transgenic tobacco, and which also provide a basis in molecular breeding of resistance adversity of Camellias in the future.
Keywords:Camellia azalea  gene clone  temperature stress  expression analysis  transgenic tobacco
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