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黄鳍鲷(Sparus latus)两种生长激素受体的cDNA克隆及组织表达分析
引用本文:马细兰,冷婷婷,刘启智,周立斌,张 勇,林浩然.黄鳍鲷(Sparus latus)两种生长激素受体的cDNA克隆及组织表达分析[J].海洋与湖沼,2011,42(6):830-838.
作者姓名:马细兰  冷婷婷  刘启智  周立斌  张 勇  林浩然
作者单位:中山大学有害生物控制与资源利用国家重点实验室 生命科学学院 水生经济动物研究所暨广东省水生经济动物良种繁育重点实验室;华南师范大学生命科学学院; 惠州学院生命科学系 生物技术研究所;中山大学有害生物控制与资源利用国家重点实验室 生命科学学院 水生经济动物研究所暨广东省水生经济动物良种繁育重点实验室;中山大学有害生物控制与资源利用国家重点实验室 生命科学学院 水生经济动物研究所暨广东省水生经济动物良种繁育重点实验室;惠州学院生命科学系 生物技术研究所;中山大学有害生物控制与资源利用国家重点实验室 生命科学学院 水生经济动物研究所暨广东省水生经济动物良种繁育重点实验室;中山大学有害生物控制与资源利用国家重点实验室 生命科学学院 水生经济动物研究所暨广东省水生经济动物良种繁育重点实验室
基金项目:国家重点基础研究发展计划(973 计划)项目, 2010CB126302 号; 广东省自然科学基金资助项目, 9451601501001986 号; 广东省教育部产学研结合项目, 2010B090400551 号
摘    要:采用RT-PCR方法克隆了黄鳍鲷两种生长激素受体(Growth hormone receptor,GHR)的cDNA序列,序列分析表明:GHR1开放阅读框为1935bp,共编码645个氨基酸,GHR2开放阅读框为1749bp,共编码583个氨基酸,GHR1与GHR2的氨基酸同源性为36.7%。GHR1和GHR2在分子结...

关 键 词:黄鳍鲷  生长激素受体  cDNA克隆  Real-time  RT-PCR  组织表达
收稿时间:2011/2/15 0:00:00
修稿时间:2011/4/21 0:00:00

cDNAs CLONING AND TISSUES EXPRESSION OF TWO GROWTH HORMONE RECEPTORS IN YELLOW-FIN BREAM SPARUS LATUS
MA Xi-Lan,LENG Ting-Ting,LIU Qi-Zhi,ZHOU Li-Bin,ZHANG Yong and LIN Hao-Ran.cDNAs CLONING AND TISSUES EXPRESSION OF TWO GROWTH HORMONE RECEPTORS IN YELLOW-FIN BREAM SPARUS LATUS[J].Oceanologia Et Limnologia Sinica,2011,42(6):830-838.
Authors:MA Xi-Lan  LENG Ting-Ting  LIU Qi-Zhi  ZHOU Li-Bin  ZHANG Yong and LIN Hao-Ran
Institution:State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University;School of Life Sciences, South China Normal University; Departm;State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University;State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University;Department of Life Science, Institute of Biotechnology, Huizhou University;State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University;State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University
Abstract:Growth hormone (GH) has many important physiological roles in the control of growth, metabolism and reproduction, which is mediated by growth hormone receptor (GHR). In this study, two cDNAs encoding GHR were isolated from the liver of yellow-fin bream Sparus latus. The two cDNAs, one consisting of 1935bp and the other of 1749bp, encoding for putative 645- and 583-amino acid GHR (designated GHR1 and GHR2, respectively), shared 36.7% identity in deduced amino acid sequence. GHR1 and GHR2 showed the conserved structural characteristics of GHR family, including the FGEFS motif, the box1 and box2 regions, extracellular cysteine residues and intracellular tyrosine residues. However, there were differences of structural features between the two receptors as well. GHR2 lacked one pair of extracellular cysteines and 4 intracellular tyrosine residues which were conservative in GHR1. The structural discrepancies thus undoubtedly indicated the distinct biological functions of GHR1 and GHR2. Real-time RT-PCR analysis showed that both GHR1 and GHR2 mRNAs were presented in all tissues tested and expressed extremely highly in the liver. In most tissues, GHR2 expressed significantly higher than GHR1. The expression distinction of GHR1 and GHR2 in pituitary and peripheral tissues like liver, muscle, spleen, kidney and gonad indicated that the two receptors may have different biological functions.
Keywords:Yellow-fin bream  Sparus latus    Growth hormone receptor    cDAN clone    Real-time PCR    Tissue expression
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