| 烟草脱落酸受体基因NtPYR1和NtPYL9的克隆及表达模式分析 |
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| 引用本文： | 黄佳,夏玉珍,赵影影,史艳梅,李锋,金立锋,谢贺,魏攀,王晨,杨军,陈继峰,林福呈,王燃. 烟草脱落酸受体基因NtPYR1和NtPYL9的克隆及表达模式分析[J]. 烟草科技, 2015, 48(7): 1-8. DOI: 10.16135/j.issn1002-0861.20150701 |
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| 作者姓名： | 黄佳 夏玉珍 赵影影 史艳梅 李锋 金立锋 谢贺 魏攀 王晨 杨军 陈继峰 林福呈 王燃 |
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| 作者单位： | 1.1. 郑州大学生命科学学院, 郑州高新技术产业开发区科学大道100号 450001;2.2. 中国烟草总公司郑州烟草研究院, 郑州高新技术产业开发区枫杨街2号 450001;3.3. 红塔烟草(集团)有限责任公司, 云南省玉溪市红塔大道118号 653100;4.4. 郑州大学化学与分子工程学院, 郑州高新技术产业开发区科学大道100号 450001;5.5. 云南省烟草农业科学院, 昆明市圆通街33号 653100 |
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| 基金项目： | 中国烟草总公司郑州烟草研究院科技项目"烟草类胡萝卜素含量的遗传调控和材料验证"(902013CZ0620)和"烟草萜类化合物合成关键基因Ntggpps功能分析和调控机制研究"(902012CZ0340) |
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| 摘 要： | 为揭示烟草脱落酸(ABA)受体基因NtPYR1和NtPYL9的生物学功能,以拟南芥PYR1和PYL9基因为探针,在NCBI中通过同源比对查找普通烟草表达序列标签(Expressed sequence tag,EST)序列,将EST序列进行拼接并设计特异性引物,从普通烟草红花大金元c DNA文库中克隆出NtPYR1和NtPYL9基因,其开放阅读框长分别为678 bp和564 bp,分别编码225个和187个氨基酸。NtPYR1和NtPYL9蛋白都具有一个保守的疏水性结构域,同属于PYR/PYL/RCAR ABA受体基因家族,NtPYR1和NtPYL9与番茄同源蛋白的相似性分别达到79.10%和95.24%。遗传聚类分析结果显示:NtPYR1和NtPYL9与番茄和马铃薯同源基因的遗传进化距离最近,说明PYR1和PYL9在茄科植物中较为保守。定量PCR对烟草不同组织表达模式分析表明,NtPYR1和NtPYL9在烟草不同组织中均有表达,分别在子叶和须根中的表达量最高。NtPYR1和NtPYL9表达均受ABA抑制,同时受H2O2诱导,说明两基因可能参与烟草的抗逆生理过程。
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| 关 键 词： | 烟草 脱落酸(ABA) 受体基因 NtPYR1 NtPYL9 克隆 表达模式 |
| 收稿时间： | 2014-06-30 |
Cloning and Expression Pattern Analysis of ABA Receptor Genes NtPYR1 and NtPYL9 in Nicotiana tabacum |
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| HUANG Jia,XIA Yuzhen,ZHAO Yingying,SHI Yanmei,LI Feng,JIN Lifeng,XIE He,WEI Pan,WANG Chen,YANG Jun,CHEN Jifeng,LIN Fucheng,WANG Ran. Cloning and Expression Pattern Analysis of ABA Receptor Genes NtPYR1 and NtPYL9 in Nicotiana tabacum[J]. Tobacco Science & Technology, 2015, 48(7): 1-8. DOI: 10.16135/j.issn1002-0861.20150701 |
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| Authors: | HUANG Jia XIA Yuzhen ZHAO Yingying SHI Yanmei LI Feng JIN Lifeng XIE He WEI Pan WANG Chen YANG Jun CHEN Jifeng LIN Fucheng WANG Ran |
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| Affiliation: | 1.1. College of Life Science, Zhengzhou University, Zhengzhou 450001, China;2.2. Zhengzhou Tobacco Research Institute of CNTC, Zhengzhou 450001, China;3.3. Hongta Tobacco(Group)Co. Ltd., Yuxi 653100, Yunnan, China;4.4. College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450001, China;5.5. Yunnan Academy of Tobacco Agricultural Sciences, Kunming 653100, China |
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| Abstract: | In order to reveal the biological function of abscisic acid(ABA) receptor genes,NtPYR1 and NtPYL9,in Nicotiana tabacum L.(N.tabacum),the encoding sequences of PYR1 and PYL9 in Arabidopsis thialianawere used as probes to find out homologous expressed sequence tags(ESTs) from N.tabacum genome in NCBI.Specific primers were designed following EST stitching,and NtPYR1 and NtPYL9 genes were cloned from cDNA library of cv.Honghuadajinyuan(N.tabacum).The open reading frames(ORFs) of NtPYR1 and NtPYL9 were 678 bp and 564 bp in length and encoded proteins of 225 and 187 amino acids,respectively.Both NtPYR1 and NtPYL9 contained a conserved hydrophobic domain and belonged to PYR/PYL/RCAR ABA receptor gene family.The similarity between NtPYR1/NtPYL9 and their homologous proteins in Solanum lycopersicum reached 79.10% and 95.24%,respectively.The results of phylogenetic analysis showed that the genetic distances between NtPYR1/NtPYL9 and their homologous genes in tomato and potato were the nearest,which indicated that PYR1 and PYL9 genes were relatively conserved in Solanaceae family.The quantitative PCR analysis of the expression patterns of NtPYR1 and NtPYL9 showed that the two could be expressed in various tissues,particularly in cotyledons and fibrous roots.The expression of NtPYR1 and NtPYL9 could be inhibited by ABA,while induced by H2O2,it implied that they might take part in the stress response process in tobacco plants. |
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