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园艺学报 ›› 2014, Vol. 41 ›› Issue (5): 907-914.

• 蔬菜 • 上一篇    下一篇

洋葱成花素基因AcFT 的克隆与表达分析

刘彬昕,王 勇*,陈 典,韦贺远   

  1. 东北农业大学园艺学院,农业部东北地区园艺作物生物学与种质创制重点实验室,哈尔滨 150030
  • 出版日期:2014-05-25 发布日期:2014-05-25
  • 基金资助:

    公益性行业(农业)科研专项项目(200903018)

Molecular Cloning and Expression Analysis of AcFT Florigen Gene in Allium cepa

  1. Department of Horticulture,Key Laboratory of Biology and Genetic Improvement of Horticultural Crops,Northeast
    Region,Ministry of Agriculture,The Northeast Agriculture University,Harbin 150030,China
  • Online:2014-05-25 Published:2014-05-25

摘要: 以春化后但尚未抽薹的洋葱品系‘1007’的叶片为试材,采用RT-PCR 结合RACE 的方法
克隆得到了洋葱成花素基因的cDNA 全长序列,将其命名为AcFT(GenBank 登录号为KF913629)。该基
因cDNA 全长791 bp,开放读码框为534 bp,推测其编码的蛋白由177 个氨基酸残基组成,等电点为7.89,
分子量为19.8 kD。将AcFT 与大葱、鸢尾等植物的成花素氨基酸序列进行同源性比对,结果显示洋葱与
其他植物的氨基酸序列同源性均在65%以上,其中洋葱与大葱的成花素氨基酸的同源性高达98.31%。实
时荧光定量RT-PCR 分析结果表明,洋葱AcFT 基因在抽薹前后的根、叶鞘、叶片、假茎和花序等不同部
位均有表达,尤以春化后抽薹前的叶片中表达量最高。

关键词: 洋葱, AcFT 基因, RACEPCR, 荧光定量, 表达分析

Abstract: The florigen gene which designated as AcFT isolated from the leaf of Allium cepa line,
‘1007’from vernalization period to bolting period(GenBank accession No. KF913629). The full-length
cDNA of florigen gene in A. cepa was obtained by RT-PCR and Rapid Amplification of cDNA Ends. The
cDNA sequence of AcFT was 791 bp long and the open reading frame was 534 bp long which could
encode a putative protein of 177 amino acids with a molecular weight of 19.8 kD and a theoretical pI of
7.89. Compared and analyzed the amino acid sequence of florigen gene with Allium fistulosum,Iris fulva
and so on,the A. cepa shared over 65% nucleotide sequence similarity with others and the similarity of
amino acids with the florigen gene in A. fistulosum is 98.31%. Fluorescence quantitative RT-PCR system
followed was established to examine the expression of AcFT. As a result,the AcFT gene from A. cepa
detected during th e different tissues that was root leaf sheath,leaf,stem and inflorescence from bolting to
vernalization,and it was highly expressed in leaves before bolting after vernalization.

Key words: Allium cepa, AcFT gene, RACEPCR, fluorescence quantitative, expression analysis

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