刘玉姣, 朱华平, 卢迈新, 刘志刚, 曹建萌, 高风英, 可小丽. 罗非鱼催乳素I基因的组织分布及盐胁迫对其表达的影响[J]. 南方水产科学, 2014, 10(6): 51-58. DOI: 10.3969/j.issn.2095-0780.2014.06.008
引用本文: 刘玉姣, 朱华平, 卢迈新, 刘志刚, 曹建萌, 高风英, 可小丽. 罗非鱼催乳素I基因的组织分布及盐胁迫对其表达的影响[J]. 南方水产科学, 2014, 10(6): 51-58. DOI: 10.3969/j.issn.2095-0780.2014.06.008
LIU Yujiao, ZHU Huaping, LU Maixin, LIU Zhigang, CAO Jianmeng, GAO Fengying, KE Xiaoli. Effect of salinity stress on expression of PRLⅠgenes from tilapias and their distribution in different tissues[J]. South China Fisheries Science, 2014, 10(6): 51-58. DOI: 10.3969/j.issn.2095-0780.2014.06.008
Citation: LIU Yujiao, ZHU Huaping, LU Maixin, LIU Zhigang, CAO Jianmeng, GAO Fengying, KE Xiaoli. Effect of salinity stress on expression of PRLⅠgenes from tilapias and their distribution in different tissues[J]. South China Fisheries Science, 2014, 10(6): 51-58. DOI: 10.3969/j.issn.2095-0780.2014.06.008

罗非鱼催乳素I基因的组织分布及盐胁迫对其表达的影响

Effect of salinity stress on expression of PRLⅠgenes from tilapias and their distribution in different tissues

  • 摘要: 采用同源克隆方法从橙色莫桑比克罗非鱼(Oreochromis mossambicus)、荷那龙罗非鱼(O.hornorum)及其正反交子代垂体中克隆了催乳素Ⅰ基因(PRLⅠ),并对其核苷酸序列和推导的氨基酸序列进行了比对分析。结果显示,4种罗非鱼的PRLⅠ基因序列长度均为798 bp,ORF长639 bp,共编码212个氨基酸;橙色莫桑比克罗非鱼和荷那龙罗非鱼仅在31号位点存在一个氨基酸残基差异。用qPCR方法分析橙色莫桑比克罗非鱼和荷那龙罗非鱼PRLⅠ基因在不同组织或器官中的表达,结果表明罗非鱼PRLⅠ基因在垂体中的表达量最高,在其他组织中的表达量较低;盐胁迫后4种罗非鱼垂体中的PRLⅠmRNA水平均显著降低,而在其他组织中的表达变化不大。由此可知PRLⅠ基因主要在垂体表达,参与罗非鱼的渗透压调节。

     

    Abstract: The prolactinⅠ(PRLⅠ) genes were cloned from pituitary glands of Oreochromis mossambicus, O.hornorum and their hybrids by homology cloning approach. The cDNA sequences and amino acid sequences deduced from them were analyzed through alignment. The results show that PRLⅠgenes from the four different species of tilapia consisted of 798 bp including open reading frame (ORF) of 639 bp, and encoded a putative protein of 212 amino acids. There was onlyamino acid residue difference between O.mossambicus and O.hormorum at the 31st site. The expression of PRLⅠgenes in different tissues and organs of O.mossambicus and O.hornorum as well as the relative expression of PRLⅠgenes of the four species of tilapia under salt stress were analyzed by real time quantitative PCR (qPCR). The results reveal that PRLⅠtranscript was detected at high level in pituitary and lowlevel in other tissues and organs. The expression of PRLⅠdecreased significantly after exposure to salt stress in pituitary. These results suggest that PRLⅠgenes play an important role in theosmoregulation of tilapia.

     

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