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园艺学报 ›› 2015, Vol. 42 ›› Issue (11): 2306-2314.doi: 10.16420/j.issn.0513-353x.2015-0513

• 研究报告 • 上一篇    下一篇

茶树硫酸盐转运蛋白基因CsSUL3.5 的克隆与表#br# 达分析

胡玉荣1,岳 川1,周 超2,黄玉婷1,曹红利1,郝心愿1,王新超1,
曾建明1,*   

  1. 1 中国农业科学院茶叶研究所,国家茶树改良中心/农业部茶树生物学与资源利用重点实验室,杭州 310008;2 西
    南大学食品科学学院,重庆 400715
  • 出版日期:2015-11-25 发布日期:2015-11-25
  • 基金资助:

    国家现代农业产业技术体系建设专项资金项目(CARS-23);中国农业科学院科技创新工程项目(CAAS-ASTIP-2014-TRICAAS);
    浙江省农业新品种选育重大科技专项(2012C12905)

Cloning and Expression Analysis of Sulfate Transporter CsSUL3.5 Gene in#br# Tea Plant

HU Yu-rong1,YUE Chuan1,ZHOU Chao2,HUANG Yu-ting1,CAO Hong-li1,HAO Xin-yuan1,WANG#br# Xin-chao1,and ZENG Jian-ming1,*   

  1. 1Tea Research Institute of the Chinese Academy of Agricultural Sciences,National Center for Tea Improvement/Key
    Laboratory of Tea Biology and Resources Utilization,Hangzhou 310008,China;2College of Food Science,Southwest
    University,Chongqing 400715,China
  • Online:2015-11-25 Published:2015-11-25

摘要:

采用电子克隆与RT-PCR 相结合的方法获得茶树硫酸盐转运蛋白(CsSUL3.5)的cDNA 序
列,并进行了相关生物信息学分析。克隆到茶树CsSUL3.5 cDNA 序列2 017 bp(GenBank 登录号
KP984500),包含完整的开放阅读框(ORF)1 914 bp,编码637 个氨基酸。生物信息学分析显示,CsSUL3.5
编码的蛋白分子量为70.38 kD,无信号肽,是疏水性的非分泌蛋白,有11 个跨膜区;与其他物种相似性
均在60%以上,与烟草的相似性最高(74%),具有硫酸盐转运蛋白家族典型的保守结构域和空间结构,
属于硫酸盐转运蛋白家族。系统进化分析表明茶树的CsSUL3.5 属于第3 亚家族,与芝麻的关系比较近。
荧光定量PCR 表明该基因在茶树幼苗根与成熟叶中均有表达;Na2SO4 与Na2SeO4 处理均能显著诱导
CsSUL3.5 的表达。

关键词: 茶树, CsSUL3.5, 硒, 克隆, 表达分析

Abstract:

The cDNA of putative sulfate transporter(CsSUL3.5)gene(GenBank accession number
KP984500)was cloned from tea plant[Camellia sinensis(L.)O. Kuntze]. Bioinformatics analysis
indicated that the cDNA of CsSUL3.5 containing 1 914 bp ORF encoded 637 amino acids residues with a
putative molecular mass of 70.38 kD. It was predicted that CsSUL3.5 was a non-secretory protein without
a signal peptide. CsSUL3.5 could be located in the plasma membrane with 11 transmembrane domains.
Further analyses showed that CsSUL3.5 had the typically conserved domain and the highest identity(74%)with Sulfate Transporter 3.5 of Nicotiana sylvestris. The real-time PCR analysis showed that
CsSUL3.5 transcripts were significantly increased upon the treatment of Na2SO4 and Na2SeO4.

Key words: tea plant, CsSUL3.5, selenium, cloning, expression analysis

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