| 引用本文: | 高 沿,胡超群,任春华,钱 璟,何香燕,江 晓,黄 文.凡纳滨对虾水孔蛋白-4的cDNA克隆及盐度胁迫对其肝胰腺mRNA表达水平的影响[J].海洋科学,2017,41(2):61-70. |
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| 凡纳滨对虾水孔蛋白-4的cDNA克隆及盐度胁迫对其肝胰腺mRNA表达水平的影响 |
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高 沿1,2, 胡超群1, 任春华1, 钱 璟1, 何香燕1,2, 江 晓1, 黄 文1
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1.中国科学院 南海海洋研究所, 中国科学院热带海洋生物资源与生态重点实验室 广东省应用海洋生物学重点实验室;2.中国科学院大学
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| 摘要: |
| 为了探索水孔蛋白(Aquaporin, AQP)在凡纳滨对虾(Litopenaeus vannamei)渗透压调节过程中作用, 本研究通过RACE方法获得克隆的凡纳滨对虾AQP(命名为LvAQP4)的cDNA全长序列, 并分析了盐度胁迫对其肝胰腺mRNA表达的影响。结果发现:LvAQP4 cDNA序列全长为1 048 bp, 其中包括75 bp的5＇UTR, 187 bp的3＇UTR 和786 bp的ORF。根据ORF序列推导出LvAQP4编码261个氨基酸, 预测其分子质量为27.85 kDa, 等电点为8.11。推导的氨基酸序列与其他甲壳物种的AQP相似度为48.8%到97.3%。进化分析显示LvAQP4属于AQP1-like亚族、AQP4类。定量PCR(qPCR)检测到LvAQP4在不同组织中均有表达, 其中鳃的表达量最高, 肝胰腺、肌肉、脑和眼柄中也较高, 而血淋巴、肠、胃和胸神经节中表达量则较低。在高盐(盐度40)刺激下, 凡纳滨对虾的肝胰腺LvAQP4 mRNA表达量会随着时间推移而上升, 到6 h达到最高, 而后逐步下降。而在低盐(盐度4)刺激下, 凡纳滨对虾的肝胰腺LvAQP4 mRNA表达量并无明显变化。在原代分离和培养的肝胰腺细胞中, 培养液中加入额外的NaCl会剂量依赖地提高LvAQP4 mRNA表达水平。同样, 通过在培养液中额外加入蔗糖提高培养液渗透压,也会剂量依赖地提高LvAQP4 mRNA表达水平, 但作用不如NaCl明显。这些结果表明盐度与肝胰腺LvAQP4的表达量有关, LvAQP4对凡纳滨对虾的渗透压调节具有非常重要的作用。 |
| 关键词: 凡纳滨对虾(Litopenaeus vannamei) LvAQP4 盐度胁迫 渗透压调节 |
| DOI：10.11759/hykx20160201003 |
| 分类号: |
| 基金项目:广东省中国科学院全面战略合作专项(2013B091300020);广东省省级科技计划项目(2014B030301064, 2015B020231007); 国家高技术研究发展计划(“863”计划)(2012AA10A404-4) |
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| Molecular cloning of aquaporin-4 (AQP4) gene in the Pacific white shrimp (Litopenaeus vannamei) and the effect of salinity stress on its expression in hepatopancreas |
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GAO Yan,HU Chao-qun,REN Chun-hua,QIAN Jing,HE Xiang-yan,JIANG Xiao,HUANG Wen
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| Abstract: |
| In this study, to explore the function of aquaporin (AQP) in the osmoregulation of Litopenaeus vannamei, the full-length cDNA of L. vannamei aquaporin-4 (termed as LvAQP4) was cloned by RACE method, and the effect of salinity stress on the transcriptional expression of LvAQP4 in the hepatopancreas was examined. The results showed that the full length cDNA of LvAQP4 was 1048 bp in length, containing a 75 bp 5＇UTR, a 187 bp 3＇UTR, and a 786 bp ORF that encode for a deduced protein of 261 amino acids with the estimated molecular mass of 27.85 kDa and an isoelectric point of 8.11. The LvAQP4 protein shared identities from 48.8% to 97.3% with its counterparts in other decapod species. Additionally, the phylogenetic analysis suggested that LvAQP4 belonged to AQP1-like subfamily and clustered with other AQP4s. Quantitative real-time PCR (qPCR) showed that the expression of LvAQP4 was ubiquitous, with the highest expression in the gills. The expression levels of LvAQP4 were also high in the hepatopancreas, muscle, brain, and eyestalk but low in hemocytes, intestine, stomach, and thoracic ganglion. Under hypersalinity stress (40), the expression levels of LvAQP4 mRNA in the hepatopancreas increased consistently from the beginning to 6 h, reaching the highest level at 6 h, and then decreased after that. Under hypersalinity stress (4), on the contrary, the mRNA levels of LvAQP4 showed no significant change. In the hepatopancreatic primary cells, the expression levels of LvAQP4 mRNA exhibited a dose-dependent upregulation when increased dosage of NaCl was added. Similar results were observed with addition of sucrose in the culture medium to increase the osmotic pressure, but the effect of sucrose on LvAQP4 transcripts was weaker than that with NaCl. These results suggested that the expression of LvAQP4 in the hepatopancreas was affected by salinity and LvAQP4 may play important roles in the osmoregulation of L. vannamei. |
| Key words: Litopenaeus vannamei LvAQP4 salinity stress osmoregulation |
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