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园艺学报 ›› 2017, Vol. 44 ›› Issue (7): 1335-1343.doi: 10.16420/j.issn.0513-353x.2017-0187

• 研究论文 • 上一篇    下一篇

津田芜菁BrPIP1 的克隆及其在非生物胁迫下的表达分析

宋 珊,马 璇,闫海芳*   

  1. 东北林业大学生命科学学院,哈尔滨 150040
  • 出版日期:2017-07-25 发布日期:2017-07-25

Cloning and Expression of the BrPIP1 Gene in Brassica rapa subsp. rapa ‘Tsuda’Under Abiotic Stress

SONG Shan,MA Xuan,and YAN Haifang*   

  1. College of Life Sciences,Northeast Forestry University,Harbin 150040,China
  • Online:2017-07-25 Published:2017-07-25

摘要:

克隆得到津田芜菁(Brassica rapa ssp. rapifera‘Tsuda’)质膜内在蛋白(plasma membrane
intrinsic proteins,PIPs)基因全长cDNA 序列,命名为BrPIP1(GenBank 登录号为KJ173685),全长为
1 056 bp,开放阅读框为861 bp,编码286 个氨基酸。荧光定量PCR 分析BrPIP1 在不同组织以及其在温
度、脱水、渗透、ABA 和盐等非生物胁迫条件下幼苗中的表达表明,该基因表达具有组织特异性,在花
瓣中表达量最高,花蕾中次之;在上述非生物胁迫下表达量都有不同程度增加,暗示BrPIP1 在非生物胁
迫应答中发挥作用。

关键词: 芜菁(蔓菁), PIP1, 基因克隆, 非生物胁迫, 表达分析

Abstract:

In this study,we cloned the plasma membrane intrinsic proteins1(PIP1)gene from
Brassica rapa‘Tsuda’,which was designated as BrPIP1 with the accession number of KJ173685 in the
NCBI GenBank. The full cDNA sequence of the BrPIP1 gene has 1 056 base pairs,containing an open
reading frame of 861 bp encoding a protein of 286 amino acids. We determined the expression of the
BrPIP1 gene in different tissues and under different abiotic stress conditions , such as extreme
temperature,dehydration,adverse osmosis,abscisic acid(ABA)and salt stress by quantitative-PCR
analysis. The results demonstrated that the highest expression levels of the BrPIP1 gene could be reached
in the petal,followed by the bud,with tissue specificity. The expression of the BrPIP1 gene was
upregulated under the aforementioned stress conditions,suggesting that the BrPIP1 gene may play a role
in response of abiotic stresses.

Key words: Brassica rapa, PIP1, gene cloning, abiotic stress, gene expression