广西师范大学学报(自然科学版) ›› 2014, Vol. 32 ›› Issue (2): 175-180.

• • 上一篇    

鳜鱼Siniperca chuatsi红肌sMyHC1基因cDNA的克隆及其表达分析

易潭1,2, 刘希良2,3, 宾石玉3, 王开卓2, 吴萍2, 褚武英2, 陈韬1   

  1. 1. 湖南农业大学动物医学院,湖南长沙410128;
    2. 长沙大学生物工程与环境科学系,湖南长沙410003;
    3.广西师范大学生命科学学院,广西桂林541004
  • 收稿日期:2014-03-10 出版日期:2014-06-25 发布日期:2018-09-25
  • 通讯作者: 陈韬(1969—),男,湖南长沙人,湖南农业大学教授,博士。E-mail:chentao_114@163.com
  • 基金资助:
    国家自然科学基金资助项目(31340054);湖南省自然科学基金资助项目(14JJ2135)

Molecular Cloning and Expression Analysis of Slow Myosin Heavy Chain 1 (sMyHC1) Gene cDNA in Mandarin Fish(Siniperca chuatsi)

YI Tan1,2 , LIU Xi-liang2,3, BIN Shi-yu3, WANG Kai-zhuo2, WU Ping2, CHU Wu-ying2, CHEN Tao1   

  1. 1.College of Veterinary Medicine,Hunan Agricultural University, Changsha Hunan 410128,China;
    2. College of Biological Engineering and Environmental Science, Changsha University,Changsha Hunan 410003,China;
    3.College of Life Science, Guangxi Normal University, Guilin Guangxi 541004, China
  • Received:2014-03-10 Online:2014-06-25 Published:2018-09-25

摘要: 本研究采用同源克隆技术克隆鳜鱼红肌肌球蛋白重链1(sMyHC1)基因cDNA序列,其总长为5 940 bp。经生物信息学分析表明,鳜鱼sMyHC1基因cDNA编码区全长5 823 bp,总共编码1 940个氨基酸。序列分析表明,鳜鱼MyHC1基因cDNA存在3个ATP结合位点、3个actin结合位点、1个ELC结合位点、1个RLC结合位点和2个Loop环。对鳜鱼sMyHC1基因进行成鱼红、白肌表达分析表明,其在红肌和心肌中的表达量显著高于白肌。研究结果为深入研究鳜鱼肌纤维分型及鳜鱼肉质研究提供可靠的实验数据和理论基础。

关键词: 鳜鱼, 红肌, 肌球蛋白重链基因, 基因克隆, 序列分析

Abstract: The slow Myosin heavy chain 1 of Mandarin fish was cloned by Homologous cloning technology. The slow Myosin heavy chain 1 gene is 5 823 bp in length and encodes 1 940 amino acids. Sequence analysis showed that the slow Myosin heavy chain 1 contains three ATP binding sites,three actin binding sites, one ELC binding site,one RLC binding site and two Loops ring. The expression level in red muscle was significantly higher than that in white muscle and cardiac muscle. The above results will make contribution to provide reliable experimental data and theoretical basis for the muscle phenotype and the research of meat quility of Siniperca chuatsi.

Key words: Siniperca chuatsi, red muscle, myosin heavy chain gene, gene clone, sequence analysis

中图分类号: 

  • 753
[1] 周瑞雪,褚武英,宾石玉,等.鳜肌球蛋白轻链2基因cDNA的克隆及其发育表达分析[J].湖南师范大学自然科学学报,2009,32(3):78-83.
[2] ZHANG Jian-She,CHU Wu-ying,CHEN Jia,et al.cDNA cloning and expression analysis of myosin heavy chain (MYH) gene of the Mandarin fish, Sniperca kneri[J].Aquacuture Reseach,2009,40(4):412-418.
[3] 周瑞雪,黄斌,蒙涛,等. 鳜碱性肌球蛋白轻链基因cDNA的克隆及其发育表达分析[J].水生生物学报,2010,34(5):927-934.
[4] 刘志军,董佩佩,贾俊静,等.肌球蛋白重链MyHC基因与肉品质的关系[J].兽药与饲料添加剂,2009,3(6):28-31.
[5] 成嘉,褚武英,张建社. 鱼类肌肉组织发生和分化相关基因的研究进展[J].生命科学研究,2010,14(4):355-362.
[6] CHU Wu-ying,LIU Lu-sha,LI Yu-long,et al.Systematic identification and differential expression profiling of microRNAs from white and red muscles of Siniperca chuatsi[J]. Current Molecular Medicine,2013,13(8):1397-1407.
[7] 符贵红,张建社.鱼类肌球蛋白重链基因研究进展及展望[J].生物技术通讯,2008,19(2):306-309.
[8] WEAVER F E,STAUFTER K A,CONGHLIN D J.Myosin heavy chain expresaion in the red,white and ventricular muscle of juvenile stages of rainbow trout[J].The Journal of Experimental Zoology,2001,290(7):751-758.
[9] JOHNSTON I A,GOLDSPINK G.Themodynamic activation parameters of fish myofibrillar ATPase enzyme and evolutionary adaptations to termperature[J].Nature,1975,257:620-622.
[10] GOLDSPINK G,TURAY L,HANSEN E,et al.Switches in fish myosin genes induced by environment temperature in muscle of the carp[J].Symposia of the Society for Experimental Biology,1992,46:139-149.
[11] TAO Yan,KOBAYASHI M,FUKUSHIMA H,et al.Changes in enzymatic and structural properties of grass carp fast skeletal myosin induced by the laboratory-conditioned thermal acclimation and seasonal acclimatization[J].Fisheries Science,2005,71:195-204.
[12] CHU Wu-ying,CHEN Jia,ZHOU Rui-xue,et al.Characterization and ontogenetic expression analysis of the myosin light chains from the fast white muscle of mandarin fish Siniperca chuatsi[J].Journal of Fish Biology, 2011,78(4):1225-1238.
[13] CHU Wu-ying,FU Gui-hong,CHEN Jia,et al. Gene expression profiling in muscle tissues of the commercially important teleost,Siniperca chuatsi L. [J]. Aquaculture International,2010,18(4):667-678.
[14] NAKAYA M,WATABE S,OOI T.Differences in the thermal stability of acclimation temperature-associated types of carp myosin and its rod on differential scanning calorimetry[J]. Biochemistry,1995,34(9):3114-3120.
[15] JOWETT T.Analysis of protein and gene expression[J]. Methods in Cell Biology,1999,59:63-85.
[16] KARLSSON A H,KLONT R E,FERNANDEZ X.Skeletal muscle fibres as factors for pork quality[J].Livestock Production Science,1999,60(2/3):255-269.
[17] 赵发兰,陈敦学,农小献,等.斑鳜肌球蛋白轻链2基因cDNA的克隆及其纵向表达分析[J].生命科学研究,2011,15(1):13-18.
[18] TIDYMAN W E,MOORE L A,BANDMAN E.Expression of fast myosin heavy chain transcripts in developing and dystrophic chicken skeletal muscle[J].Developmental Dynamics,1997,208(4):491-504.
[1] 秦新民, 张渝, 刘玉洁, 郭丹妮, 李惠敏. 沙田柚S-RNase基因的克隆及序列分析[J]. 广西师范大学学报(自然科学版), 2015, 33(1): 139-145.
[2] 王开卓, 宾石玉, 李虹辉, 李玉珑, 刘知行, 张建社, 褚武英. 翘嘴鳜生长抑制素基因的克隆及其表达分析[J]. 广西师范大学学报(自然科学版), 2013, 31(4): 109-114.
[3] 赵志常, 胡福初, 胡桂兵, 王惠聪, 杨转英, 苏纯兰, 李加强. 荔枝类黄酮糖基转移酶(UFGT)基因的克隆及其原核表达研究[J]. 广西师范大学学报(自然科学版), 2011, 29(4): 104-110.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!
版权所有 © 广西师范大学学报(自然科学版)编辑部
地址:广西桂林市三里店育才路15号 邮编:541004
电话:0773-5857325 E-mail: gxsdzkb@mailbox.gxnu.edu.cn
本系统由北京玛格泰克科技发展有限公司设计开发