拟穴青蟹14-3-3基因全长cDNA的克隆及组织表达分析
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浙江大学动物科学学院,浙江大学动物科学学院,浙江大学动物科学学院,浙江大学动物科学学院,浙江大学动物科学学院

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浙江省重大科技专项农业项目(2008C12008)


The full length cDNA cloning and expression profile of 14-3-3 gene from the mud crab(Scylla paramamosain)
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College of Animal Science,Zhejiang University,College of Animal Science,Zhejiang University,College of Animal Science,Zhejiang University,College of Animal Science,Zhejiang University,College of Animal Science,Zhejiang University

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    摘要:

    采用RT-PCR及RACE技术, 从拟穴青蟹眼柄组织中克隆获得14-3-3基因cDNA全序列。序列分析结果表明:拟穴青蟹14-3-3基因全长1 112 bp, 开放阅读框长744 bp, 编码由247个氨基酸组成的蛋白, 分子量为28.086 ku, 等电点为4.675。与其他物种14-3-3基因氨基酸序列进行同源性比较分析显示, 拟穴青蟹14-3-3基因与斑节对虾14-3-3基因同源性最高(95%), 依次为墨吉对虾(93%)、苜蓿切叶蜂(92%)。聚类分析表明, 拟穴青蟹14-3-3基因氨基酸序列与斑节对虾、墨吉对虾紧密聚为一支。经荧光定量检测, 拟穴青蟹14-3-3基因在肝胰腺和肌肉中的表达量较高, 其次为鳃、眼柄、心脏和肠, 在胃中表达最少。盐度骤变实验结果表明:盐度胁迫24 h后, 盐度的下降(5)或者上升(15、20、25、30)都引起了14-3-3基因在鳃中的表达量极显著上升(P<0.01), 盐度变化的幅度越大, 14-3-3基因的表达量越多。实验结果为进一步深入研究14-3-3基因的功能及调控机理奠定基础。

    Abstract:

    Full-length cDNA sequence of 14-3-3 gene was isolated from the eyestalk of mud crab Scylla paramamosain through RT-PCR and RACE. Sequence analysis indicated that 14-3-3 gene had an open reading frame of 744 bp encoding 247aa of 28.086 ku and pI at 4.675. The amino acid sequences of 14-3-3 gene possessed 95%, 93%, 92% identity with the 14-3-3 genes of Penaeus monodon, Fenneropenaeus merguiensis, Megachile rotundata respectively. 14-3-3 protein firstly clustered with 14-3-3 proteins of Penaeus monodon and Fenneropenaeus merguiensis in the phylogenetic analysis. The expression of 14-3-3 gene in tissues was analyzed by Real-Time PCR, the result showed that 14-3-3 gene was most expressed in hepatopancreas and muscle, then in eyestalk, intestinal, heart and gill, the lest in stomach. After 24h’s stress in salinity, the expression of 14-3-3 gene increased great significantly (P<0.01) whatever the salinity reduced (5) or raise (15, 20, 25, 30). The more the salinity changed, the more the 14-3-3 gene expressed. These results will serve further studies on functions and regulation mechanism of 14-3-3 genes.

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舒妙安,张龙韬,徐宾朋,胡杭娇,郭晓令.拟穴青蟹14-3-3基因全长cDNA的克隆及组织表达分析[J].水产学报,2012,36(8):1193~1200

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  • 收稿日期:2012-02-22
  • 最后修改日期:2012-03-21
  • 录用日期:2012-06-01
  • 在线发布日期: 2012-08-22
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