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刀鲚MSTN基因的克隆及其组织表达
引用本文:杜富宽,聂志娟,徐钢春,徐跑,顾若波.刀鲚MSTN基因的克隆及其组织表达[J].中国水产科学,2014,21(4):684-692.
作者姓名:杜富宽  聂志娟  徐钢春  徐跑  顾若波
作者单位:中国水产科学研究院 淡水渔业研究中心, 农业部淡水渔业和种质资源利用重点实验室, 江苏 无锡 214081
基金项目:国家科技支撑计划项目(2012BAD26B05); 中央级公益性科研院所基本科研业务费院级专项(2012A0705); 江苏省水产三新工程重大专项(DZ2012-1).
摘    要: 运用同源克隆的方法和RACE技术, 从刀鲚(Coilia nasus)肌肉组织中克隆了肌肉生成抑制素基因(Myostatin, MSTN)cDNA全长并分析了肌肉生长抑制素基因在刀鲚不同组织的表达情况。结果表明, 刀鲚MSTN 基因的cDNA全长2 252 bp, 编码区1 125 bp, 编码374氨基酸。二级结构预测显示, 刀鲚MSTN具有MSTN家族的典型结构域, 包含PfamTGFB结构域。运用荧光定量的方法检测了该基因在刀鲚不同组织中的表达。结果显示MSTN基因在健康刀鲚肌肉和脑中呈高表达, 鳃、肝、脾、肠、肾和头肾中微量表达。根据以上研究结果认为, 刀鲚MSTN基因的序列具有高度保守性, 组织表达模式相似, 推测该基因的功能也具有高度保守性。本研究旨为MSTN基因在刀鲚后续育种工作提供基础依据。

关 键 词:刀鲚    MSTN基因    克隆    组织表达
修稿时间:2015/8/3 0:00:00

Cloning and tissue expression of the MSTN gene in Coilia nasus
DU Fukuan,NIE Zhijuan,XU Gangchun,XU Pao,GU Ruobo.Cloning and tissue expression of the MSTN gene in Coilia nasus[J].Journal of Fishery Sciences of China,2014,21(4):684-692.
Authors:DU Fukuan  NIE Zhijuan  XU Gangchun  XU Pao  GU Ruobo
Institution:Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi 214081, China
Abstract:

 Estuarine tapertail anchovy (Coilia nasus, junior synonym C. ectenes) are widely distributed throughout the Yangtze River, the coastal waters of China and Korea, and the Ariake Sound of Japan. The species is commercially important because of its nutritional value and taste. In recent years, overharvest and changes in the aquatic ecosystem almost resulted in the extinction of the species in the middle reaches of the Yangtze River. Researchers have evaluated a number of measures to conserve the species, including captive breeding in ponds, artificial propagation, and larval rearing. As a result, the immediate threat to C.nasus has been alleviated at present. However, artificially cultured C. nasus grow relatively slowly (~125 g in 2+ years) so there is a need to improve the growth rate. To determine the molecular mechanisms controlling growth and meat quality in Coilia nasus, we cloned the myostatin gene in C. nasus by homologous cloning methods. Its full-length cDNA was 2 252 bp long, with a 1 125 bp open reading frame (ORF) that encoded a 374 amino acid protein. The C. nasusu MSTN protein was predicted to contain a signal peptide sequence, conserved cysteine ​​residues, and RXXR proteolytic sites. Gene expression was deduced by qRT-PCR. The MSTN gene of C. nasus was expressed strongly in the muscle and brain, but weakly in the gills, liver, spleen, intestine, kidney, and head kidney. MSTN expression in C. nasus was not limited to skeletal muscle. Our results suggest that the biological actions of MSTN in C. nasus, and possibly in other fishes, may not be limited to skeletal muscle growth repression, but may also influence different cell types and organ systems, particularly brain cells. The MSTN gene has shown significant potential in mammalian breeding programs, and our results provide for a basis for development of breeding programs in C. nasus.

 


Keywords:Coilia nasus  MSTN gene  expression pattern
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