首页|辣椒CaCBF1A基因的克隆及非生物胁迫下表达分析

辣椒CaCBF1A基因的克隆及非生物胁迫下表达分析

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为揭示CaCBF1A基因在辣椒抗逆机制中发挥的功能,对辣椒CaCBF1A基因进行克隆与分析.以豫椒101为材料,根据参考基因组序列设计引物,通过PCR技术从辣椒基因组cDNA中获得CBF基因CaCBF1A.经生物信息学分析,该基因具有一个完整的ORF(471 bp),编码156个氨基酸.CaCBF1A编码的蛋白质包含保守的AP2 DNA结合域.对其亚细胞定位、跨膜结构进行分析,预测其定位在叶绿体中,存在跨膜结构.荧光定量PCR检测结果表明,低温、高温和盐胁迫均可诱导CaCBF1A基因的表达,其表达量在迅速达到峰值后又降低,说明CaCBF1A是一个逆境胁迫快速响应基因,推测其在辣椒抗逆机制中起着重要的作用.
Cloning and Expression Analysis of CaCBF1A Gene from Capsicum annuum L.under Abiotic Stress
To reveal the roles of CaCBF1A gene played in pepper,the CaCBF1A gene was cloned and analyzed.According to the CBF gene sequence from Capsicum annuum genome,the primer was designed.Yujiao 101 was taken as material and CaCBF1A was acquired from the genome of pepper by PCR.The bioinformatics analysis results indicated that the gene possessed complete ORF with length of 471 bp,encoding 156 amino acids.Protein encoded by CaCBF1A gene in pepper contained conservative AP2 DNA binding domain.Besides,the subcellular localization and membrane structure were analyzedJt was predicted that protein encoded by CaCBF1A was located in chloroplasts,and contained transmembrane structure.Furthermore,the results by fluorescence quantitative PCR showed that cold,high temperature and salt stress could induce the expression of CaCBF1A gene,the expression level of which was decreased rapidly after peak point.These could provide some indication that CaCBF1A was rapid response gene,which played important roles in the resistance mechanisms of pepper.

Capsicum annuum L.CBF genegene cloningabiotic stressexpression analysis

魏小春、李艳、姚秋菊、原玉香、赵艳艳、王志勇、姜俊、段俊枝、蒋武生

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河南省农业科学院园艺研究所,河南郑州450002

驻马店市农业科学院,河南驻马店463000

河南省农业科学院农业经济与信息研究所,河南郑州450002

辣椒 CBF基因 基因克隆 非生物胁迫 表达分析

国家大宗蔬菜产业技术体系豫北综合试验站项目河南省重大科技专项

CARS-25-G-27151100110400

2016

河南农业科学
河南省农业科学院

河南农业科学

CSTPCDCSCD北大核心
影响因子:0.787
ISSN:1004-3268
年,卷(期):2016.45(12)
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