石榴PgGPX基因克隆及盐胁迫下的表达分析
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国家自然科学基金(30900971)


Cloning of PgGPX Gene in Pomegranate and Its Expression Analysis under Salt Stress
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    摘要:

    该研究以‘红玉石籽’籽粒为材料,通过RACE技术克隆了石榴GPX基因,利用Real-time PCR检测石榴在不同器官中及石榴叶片在盐胁迫处理下的相对表达量。结果表明:(1)PgGPX基因cDNA全长872 bp,其中开放阅读框504 bp,编码168个氨基酸。生物信息学分析显示,该蛋白具有植物GPX的典型结构,与可可树、荔枝、甜橙、玉米等植物的GPX基因相比,具有较高的一致性,分别为90.30%、87.40%、86.80%、86.20%。(2)PgGPX在石榴的叶片、花瓣和籽粒中均有所表达,且具有组织特异性,在盐胁迫下,石榴叶片中的PgGPX表达量显著上升。推测PgGPX基因在胁迫反应中可能发挥重要作用。

    Abstract:

    In this study,the gene GPX(glutathione peroxidase) was cloned by RACE from the seeds of ‘Hongyushizi’,a cultivar of pomegranate.The expression of PgGPX in different organs of ‘Hongyushizi’ and its leaves under salt stress were analyzed by Real-time PCR.The results showed that the length of PgGPX was 872 bp and its ORF was 504 bp which encoding 168 amino acids.Bioinformatics analysis showed PgGPX possessed a typical conserved domain of GSH-Peroxidase and had high consistency with Theobroma cacao,Litchi chinensis,Ricinus communis and Zea mays as 90.30%,87.40%,86.80% and 86.20%,respectively.The real-time PCR results showed the expression of PgGPX in leaf,petal and aril were all detected and its expression had tissue specificity.The expression levels of PgGPX increased obviously under salt stress indicated that it may play an important role in stress reaction.

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彭媛媛,龚凌燕,曹丹琴,等.石榴PgGPX基因克隆及盐胁迫下的表达分析[J].西北植物学报,2014,34(9):1735-1741

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  • 在线发布日期: 2014-10-15
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