三疣梭子蟹心激肽基因克隆及在低盐适应中的功能验证
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1. 中国水产科学研究院黄海水产研究所, 农业农村部海洋渔业可持续发展重点实验室, 山东 青岛 266071;
2. 青岛海洋科学与技术国家实验室, 海洋渔业科学与食物产出过程功能实验室, 山东 青岛 266071

作者简介:

孙东方(1991-),男,硕士研究生,主要从事三疣梭子蟹遗传育种研究.E-mail:961012207@qq.com

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中图分类号:

S917

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国家自然科学基金面上项目(41576147,41776160);国家虾产业技术体系(CARS-48);山东省泰山领军人才工程高效生态农业创新类计划(LJNY2015002);中国水产科学研究院黄海水产研究所基本科研业务费资助(20603022018027);山东省重点研发计划(2018GSF121030,2016GSF115028).


Cloning of crustacean cardioactive peptide and its functional verification under low-salt adaptation in swimming crab (Portunus trituberculatus)
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1. Key Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture and Rural Affairs;Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China;
2. Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, China

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    摘要:

    采用RACE技术克隆获得三疣梭子蟹()心激肽(CCAP)基因。该基因全长606 bp,5'端非编码区72 bp,3'端非编码区108 bp,开放阅读框426 bp,编码141个氨基酸,预测分子量15.6 kD,理论等电点9.55。同源性分析表明,三疣梭子蟹CCAP与拟穴青蟹()的CCAP同源性较高,分别为85%和82%。系统进化树分析显示,三疣梭子蟹与蓝蟹首先聚为一支,之后再与拟穴青蟹相聚。组织表达分析发现,CCAP基因在胸神经节中的相对表达量最高,其次是脑和眼柄组织。通过分析CCAP基因在低盐胁迫过程中的表达规律发现,低盐可显著改变CCAP在胸神经节中的表达模式,在24 h,48 h和72 h实验组的表达量显著高于对照组(<0.05),分别为对照组的1.73,2.16和2.19倍。体外注射CCAP多肽可降低三疣梭子蟹在低盐条件下的死亡率,并诱发钠钾ATP酶(Na+/K+-ATPase)和V型ATP酶(V-ATPase)酶活力显著提高。本实验结果暗示CCAP通过调控Na+/K+-ATPase和V-ATPase活力以达到盐度适应的作用。

    Abstract:

    The swimming crab , an important marine economic animal widely distributed in China, belongs to Crustacea, Decapoda, Decapoda, is an aquatic crustacean with wide tolerance to salinity (13.7-47.7). Salinity is one of the most important environmental factors affecting the growth and development of . Ingestion, molting, growth, metabolism, immunity, and other processes in are greatly affected by salinity. Therefore, it is important to study the mechanism of salinity adaptation to breed improved salt-tolerant varieties of . In this study, random amplification of cDNA ends technology was used to clone the crustacean cardioactive peptide (CCAP) gene. The full-length CCAP gene was 606 base pairs (bp) long, including an open reading frame of 426 bp, 5' untranslated region of 72 bp, and 3' untranslated region of 108 bp, with a poly A structure. Amino acid sequence analysis showed that the CCAP gene encodes 141 amino acids with a predicted molecular weight of 15.6 kD and isoelectric point of 9.55. Homology analysis showed that the homology between CCAP of Callinectes sapidus was higher at 85% and 82%, respectively. Phylogenetic analysis showed that were clustered first, followed by . Tissue expression analysis revealed that the relative expression of the CCAP gene was highest in the in thoracic ganglia, followed by in the brain and eye stalk. Analysis of the expression pattern of the CCAP gene during low-salinity stress showed that low salinity significantly altered the expression pattern of CCAP in the thoracic ganglia; CCAP gene expression in the experimental group was significantly higher than that in the control group at 24, 48, and 72 h ( < 0.05) with values 1.73-, 2.16-, and 2.19-fold higher than that in the control group, respectively. P. trituberculatus under low-salinity conditions and the activities of Na+/K+-ATPase and V-ATPase were significantly increased. The results demonstrate that CCAP plays a protective role in under low-salinity conditions by regulating osmotic pressure and may be associated with increased Na+/K+-ATPase and V-ATPase activities to modulate the osmotic pressure balance in .

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孙东方,吕建建,高保全,环朋朋,蔡影,刘萍.三疣梭子蟹心激肽基因克隆及在低盐适应中的功能验证[J].中国水产科学,2019,26(2):261-270
SUN Dongfang, LYU Jianjian, GAO Baoquan, HUAN Pengpeng, CAI Ying, LIU ping. Cloning of crustacean cardioactive peptide and its functional verification under low-salt adaptation in swimming crab (Portunus trituberculatus)[J]. Journal of Fishery Sciences of China,2019,26(2):261-270

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  • 在线发布日期: 2019-03-27
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