• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

金线莲甘露糖-1-磷酸尿苷转移酶基因的克隆与表达分析

Cloning and Expression of Mannose-1-phosphate Guanyltransferase Gene in Anoectochilus roxburghii

  • 摘要:
      目的  甘露糖是金线莲多糖重要组成成分,对甘露糖-1-磷酸尿苷转移酶(GMP)基因进行克隆和基因表达调控分析,为进一步研究金线莲多糖的生物合成奠定基础。
      方法  以梅花山金线莲植株为材料,克隆ArGMP基因的cDNA序列和基因组序列,利用在线软件进行生物信息学分析,并对其基因表达调控模式进行qRT-PCR分析。
      结果  金线莲ArGMP基因ORF区序列长1086 bp,共编码361个氨基酸;基因组序列长度为1760 bp,含有3个内含子,GenBank登录号OQ030271。生物信息学分析表明:ArGMP蛋白是一种较稳定的、无跨膜结构的亲水蛋白,该蛋白与铁皮石斛、深圳拟兰、蝴蝶兰等兰科植物的亲缘关系较近。qRT-PCR结果显示:ArGMP基因在金线莲不同组织中的表达量差异显著,在花中的表达量最高;在不同种植温度处理条件下,25 ℃时表达量最高,高温严重抑制其表达;35 ℃高温处理不同时间显示,处理3 h后ArGMP基因表达量显著下降;而不同浓度NaCl胁迫处理对ArGMP基因表达基本无影响。
      结论  克隆了甘露糖-1-磷酸尿苷转移酶基因的cDNA序列和基因组序列,发现该基因具有组织特异性表达的特点,且该基因受温度调控,而不受盐胁迫调控,这为进一步研究金线莲多糖生物合成调控机制奠定理论基础。

     

    Abstract:
      Objective  Cloning and expression of mannose-1-phosphate guanyltransferase (GMP) gene that regulates the polysaccharide synthesis in Anoectochilus roxburghii were studied.
      Method  ArGMP cDNA and genome sequences were cloned, and bioinformatics analyzed using online software. Gene expression pattern was then determined by qRT-PCR.
      Result  The ORF of ArGMP was 1 086 bp encoded 361 amino acids with a length of 1 760 bp that contained 3 introns. It has an accession number of OQ030271 in GenBank. A stable hydrophilic protein free of a transmembrane structure, it was closely related to those of Dendrobium officinale, Apostasia shenzhenica, and Phalaenopsis equestris. Expressed differently in different tissues, the highest level was found in the flowers. The expression varied under different temperatures that peaked at 25 ℃, decreased significantly after 3 h at 35 ℃, and was severely inhibited beyond that. However, it was not affected by the stress exerted by NaCl in different concentrations.
      Conclusion  The cDNA and sequence of GMP gene from A. roburghii were successfully cloned to display a tissue-specific expression pattern that could be significantly affected by temperature but not salt stress.

     

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