首页 | 本学科首页   官方微博 | 高级检索  
     检索      

斜带石斑鱼(Epinephelus coioides)两种催乳素受体基因的 cDNA 克隆和 mRNA 表达分析
引用本文:张 勇,马细兰,陈勇智,李水生,陈华谱,刘晓春,林浩然.斜带石斑鱼(Epinephelus coioides)两种催乳素受体基因的 cDNA 克隆和 mRNA 表达分析[J].海洋与湖沼,2012,43(1):138-146.
作者姓名:张 勇  马细兰  陈勇智  李水生  陈华谱  刘晓春  林浩然
作者单位:1. 中山大学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,广州,510275
2. 华南师范大学生命科学学院,广州510631/惠州学院生命科学系生物技术研究所,惠州516007
3. 惠州学院生命科学系生物技术研究所,惠州,516007
基金项目:公益性行业(农业)科研专项, 200903046 号
摘    要:采用RT-PCR方法克隆了斜带石斑鱼两种催乳素受体(Prolactin receptor,PRLR)的cDNA序列,序列分析表明:PRLR1开放阅读框为1947bp,共编码649个氨基酸,PRLR2开放阅读框为1749bp,共编码487个氨基酸,PRLR1与PRLR2的氨基酸同源性为40.4%。用Real-time RT-PCR方法研究了PRLR1和PRLR2在各组织和早期发育不同阶段的表达情况,结果表明:PRLR1和PRLR2在所检测的12种组织中均有表达,其中以鳃、肾、肠表达量较高;PRLR1在受精期表达最高,PRLR2在视囊形成期表达最高,而且除受精卵期外PRLR2在各时期的表达量均高于PRLR1。

关 键 词:斜带石斑鱼  催乳素受体  cDNA克隆  Real-time  RT-PCR  mRNA表达
收稿时间:9/9/2011 12:00:00 AM
修稿时间:2011/11/16 0:00:00

cDNAs CLONING AND mRNA EXPRESSION OF TWO PROLACTIN RECEPTORS IN ORANGE-SPOTTED GROUPER EPINEPHELUS COIOIDES
ZHANG Yong,MA Xi-Lan,CHEN Yong-Zhi,LI Shui-Sheng,CHEN Hua-Pu,LIU Xiao-Chun and LIN Hao-Ran.cDNAs CLONING AND mRNA EXPRESSION OF TWO PROLACTIN RECEPTORS IN ORANGE-SPOTTED GROUPER EPINEPHELUS COIOIDES[J].Oceanologia Et Limnologia Sinica,2012,43(1):138-146.
Authors:ZHANG Yong  MA Xi-Lan  CHEN Yong-Zhi  LI Shui-Sheng  CHEN Hua-Pu  LIU Xiao-Chun and LIN Hao-Ran
Institution:Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, Sun Yat-Sen University;School of Life Sciences, South China Normal University;Department of Life Science, Institute of Biotechnology, Huizhou University;Department of Life Science, Institute of Biotechnology, Huizhou University;Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, Sun Yat-Sen University;Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, Sun Yat-Sen University;Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, Sun Yat-Sen University;Institute of Aquatic Economic Animals and Guangdong Provincial Key Laboratory for Aquatic Economic Animals, Sun Yat-Sen University
Abstract:Prolactin (PRL) has many important physiological roles in the control of growth, osmoregulation and reproduction, which is mediated by prolactin receptor (PRLR). In this study, two cDNAs encoding PRLR were isolated from the gill of orange-spotted grouper Epinephelus coioides. The two cDNAs, one consisting of 1947bp and the other of 1749bp, encoding for putative 649- and 487-amino acid PRLR (designated PRLR1 and PRLR2, respectively), shared 40.4% identity in deduced amino acid sequence. PRLR1 and PRLR2 showed the conserved structural characteristics of PRLR family, including the WS motif, the box1 region, extracellular cysteine residues and intracellular tyrosine residues. However, there were differences of structural features between the two receptors as well. PRLR1 has 13 intracellular tyrosine residues while PRLR2 only has 8. The structural discrepancies thus undoubtedly indicated the distinct biological functions of PRLR1 and PRLR2. Real-time RT-PCR analysis showed that both PRLR1 and PRLR2 mRNAs were presented in all tissues tested and expressed extremely highly in gill, kidney and intestine, lowly in pituitary and hypothalamus. The expressions of PRLR1 and PRLR2 in different embryo developmental stages were also detected by real-time PCR. The strongest signal was detected in the fertilized egg stage for PRLR1, while in the stage of optic vesicle and smoite formation for PRLR2. The expression level of PRLR2 is much higher than PRLR1 in all stages examined except in the fertilized egg stage. The expression distinction of PRLR1 and PRLR2 suggested that they may play different roles during early development of orange-spotted grouper.
Keywords:Orange-spotted grouper Epinephelus coioides    Prolactin receptor    cDNA clone    Real-time RT-PCR  mRNA expression
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《海洋与湖沼》浏览原始摘要信息
点击此处可从《海洋与湖沼》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号