赵超平, 郭华阳, 张健, 朱克诚, 郭梁, 张楠, 刘宝锁, 杨静文, 张殿昌. 卵形鲳鲹AQP1a分子特征及其对急性盐度胁迫的表达响应[J]. 南方水产科学, 2018, 14(4): 56-65. DOI: 10.3969/j.issn.2095-0780.2018.04.007
引用本文: 赵超平, 郭华阳, 张健, 朱克诚, 郭梁, 张楠, 刘宝锁, 杨静文, 张殿昌. 卵形鲳鲹AQP1a分子特征及其对急性盐度胁迫的表达响应[J]. 南方水产科学, 2018, 14(4): 56-65. DOI: 10.3969/j.issn.2095-0780.2018.04.007
ZHAO Chaoping, GUO Huayang, ZHANG Jian, ZHU Kecheng, GUO Liang, ZHANG Nan, LIU Baosuo, YANG Jingwen, ZHANG Dianchang. Molecular characteristics and expression analysis of AQP1a from Trachinotus ovatus under acute salinity stress[J]. South China Fisheries Science, 2018, 14(4): 56-65. DOI: 10.3969/j.issn.2095-0780.2018.04.007
Citation: ZHAO Chaoping, GUO Huayang, ZHANG Jian, ZHU Kecheng, GUO Liang, ZHANG Nan, LIU Baosuo, YANG Jingwen, ZHANG Dianchang. Molecular characteristics and expression analysis of AQP1a from Trachinotus ovatus under acute salinity stress[J]. South China Fisheries Science, 2018, 14(4): 56-65. DOI: 10.3969/j.issn.2095-0780.2018.04.007

卵形鲳鲹AQP1a分子特征及其对急性盐度胁迫的表达响应

Molecular characteristics and expression analysis of AQP1a from Trachinotus ovatus under acute salinity stress

  • 摘要: 水通道蛋白(aquaporin,AQPs)是由内在膜蛋白组成的超家族,介导水分子的跨膜运输,对渗透压调节具有重要作用。为研究AQP1a在急性盐度胁迫下对卵形鲳鲹 (Trachinotus ovatus)的渗透压调节作用,该研究获得AQP1a基因。基因全长1 078 bp,开放阅读框786 bp,编码261个氨基酸,具有MIP家族特有序列(HINPAVTLG)和2个天冬酰胺−脯氨酸−丙氨酸蛋白基序。qRT-PCR结果显示,AQP1a在11个被测组织中均有表达,在性腺中的表达量最高,其次是鳃和肠,在肌肉中表达量最低。在急性盐度胁迫下,当转入淡水时,AQP1a在鳃的表达量在第4小时显著上升,而在肾和肠中没有显著变化;当转入盐度10和20海水时,鳃中AQP1a的表达量在第2和第4小时显著升高,然后下降趋于稳定;转入盐度10海水时,肠中AQP1a的表达量均上升,肾中AQP1a的表达量呈先上升后下降趋势;转入盐度20海水时,肠中AQP1a的表达量仅在第4、第8和第48小时显著上升,肾中AQP1a的表达量在第12小时达到最大;转入盐度40海水中,鳃中AQP1a的表达量明显下降,相反,在肾和肠中AQP1a的表达量均明显上调。这些结果反映了AQP1a在不同组织中的功能特异性,证实了AQP1a在卵形鲳鲹盐度适应中起重要作用。

     

    Abstract: Aquaporin, a superfamily of internal membrane proteins that mediate transmembrane transport of water molecules, plays an important role in osmotic adjustment. AQP1a gene was obtained in order to study the role of AQP1a in osmoregulation of Trachinotus ovatus under acute salinity stress. The sequence of AQP1a gene was 1 078 bp with an open reading frame of 786 bp encoding 261 amino acids. The structural analysis shows that it has the structural characteristics of MIP family-specific sequence (HINPAVTLG) and two asparagine-proline-alanine (NPA) motifs. The qRT-PCR results show that AQP1a was distributed in the 11 tested tissues, highest in gonads and then in gill, intestine and liver, lowest in muscle. Under acute salinity stress, after being transfered to fresh water, the expression of AQP1a in gill increased at 4th hour, while there was no significant change in the expression in kidney and intestine. After being transfered to 10‰ and 20‰ salinity seawater, the expression of AQP1a in gill increased significantly at 2nd and 4th hour, and then decreased gradually. When being transferred to 10‰ salinity seawater, the expression of AQP1a in intestine increased. In kidney, the expression of AQP1a first increased and then decreased. When being transferred to 20‰ salinity seawater, the expression of AQP1a in intestine only increased significantly at 4th, 8th and 48th hour. In kidney, the expression of AQP1a reached the maximum at 12th hour. In 40‰ salinity seawater, the expression of AQP1a in gill decreased significantly. On the contrary, the expression of AQP1a in kidney and intestine were significantly up-regulated. The results reveal that the specificity of AQP1a functions in different tissues and plays an important role in T.ovatus salinity adaptation.

     

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