重组人-α干扰素基因(Hu-IFN-α)在草鱼体内的整合与表达
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
草鱼年产量占我国淡水鱼总产量的20%。其生长快、饲料来源广、饲养成本低和肉味鲜美。但草鱼病害多,危害严重,目前草鱼由苗种养至成鱼的成活率仅为10-15%,每年给我国淡水养殖业造成数亿元经济损失。特别是病毒性的草鱼出血病,流行季节长,发病死亡率高,因此,对草鱼出血病的有效防治一直是世界各国水产科学工作者艰苦探索而又未能找到理想解决办法的世界性难题。现代分子生物学技术突飞猛进的发展为我们切底解决这一难题提供了可能性和有效途径。综观国内外近些年来对转基因鱼的研究及结果证明,通过转基因定向培育出符合人们所需要的优良鱼种是完全可能的,也是十分有意义的。通过基因转移进行鱼类抗病育种研究,是鱼类转基因研究中的一个新的方向。
     人-α干扰素(hu-α-IFN)是人体因病毒感染或其它诱生剂作用等所产生的一类非特异性抗病毒物质,是调节细胞功能的一类重要的糖蛋白。其作用是通过与细胞膜上的特异性受体结合,引发级联性的信号放大过程,将信号最后传递到细胞核内,对一系列基因的表达进行调控,并引发各种生理反应,整体性地提高自身的免疫和抗病毒能力。本研究的目的在于以人的α-干扰素基因(IFN-α)作为目的基因,与鲤鱼β-肌动蛋白基因启动子在体外重组,利用原核显微注射转基因技术将人-α干扰素基因导入草鱼基因组而开展的抗病转基因草鱼育种研究,其结合了干扰素和基因工程育种抗草鱼出血病病毒的优点,以期获得对草鱼出血病具有天然抗性的转基因鱼,并在此基础上培育出草鱼抗病新品系。从而探索出一种从根本上解决草鱼出血病的有效途径。
     实验通过将hu-α-IFN基因重组分子采用显微注射法将这种重组基因转化草鱼1-2细胞期的受精卵,即以Narashige显微注射仪,将5nl DNA(约10~6~10~7分子)直接注射到选择好的受精卵核的动物极上。2000年共显微注射32197粒草鱼受精卵,出苗12945尾草鱼鱼苗,经孵化培育最后获得1120尾五寸左右草鱼,对1120尾草
    
    鱼提取血液总DNA进行PCR和Southern杂交检测,2000年转导的草鱼的PCR检
    测结果,有672尾草鱼即600k转化个体的总DNA能扩增出一条485kb的特异分子
    带,说明转化个体整合有huJ-IFN基因,经Southern杂交进一步证实,转入的抗病
    相关基因己在转基因草鱼体内染色体上得以整合,但整合位点没有固定区域,整合
    的拷贝数存在较大差异。对 PCR呈阳性的草鱼 672尾个体进行 ELISA检测,在 158
    尾草鱼中检出有人a-干扰素的表达即阳性率为23.5%,但基因表达水平在个体间有
    很大差异,对ELISA检测呈阳性的转基因草鱼接种草鱼出血病病毒的攻毒试验,证
    明了转基因鱼对草鱼出血病毒的抗性比普通草鱼提高了60{0儿
The annual yield of grass carp covers 20% in total output of the fresh water fish,which is fast growing and tastes delicious,besides, the forages of grass carp are various ,with a lower cost of raising,However, at present,the serious diseaes of grass carp results in a lower survival rate 10-15%,which cause more then billions yuan economic losses per year to the fresh water cultiuation ,especially, Hemorrhagic virus of carp lasts for a long period of time and features a high death rate,therefore,it' s a woed-wide problem for the aquacultural scientific researchers to discover an effective settlement ,which is still under the discussion. The rapid development of modem molecular biology technique suppies a possible and efficient way for us to solove the problem completely with a comprehensive researches results to transgenic fish in recent years both domestic and aboard,it proves that it' s possible and makes great senses to cultivate a high quality fish to meet the satisifaction of the people . Making anti-dis
    
    
    ease breeding researches of fish by transfer
    gene is a new direction in transfergene researches offish.
    Hu-α -IFN is a sort of biological activity mass of
    broad-spectrum antivirus and have evdient effictiveness to varities of viral-disease . it was important glucoprotein modulating cell functions by combination to idiosyncrasy receptor on cell membrane, which inducing process of cascade signal magnifying, then passing signals into nucleus to induce the modulation of the serial gene expression and viarous physiological reaction, and inhence immunity and antivirus. Take advantage of the character of hu- α -IFN, The recombination gene was recombinated hu- α -IFN gene
    and carp β -actin gene promoter, then it was migrate into the body of lower vertebrate grass carp. Through studing its integration, expression and antivirus, expected to gain a new kind of grass carp assumed notable antivirus of Hemorrhagic virus of carp . the research adopts that Hu- α -IFN gene were introduced into the nuclei of oocytes or cytoplasm of Grass carp to develop anti-disease transgenic grass carp breeding researches,combing the adva
    ntag
    e of Hu- α -IFN gene and breeding by Genetic engineering,with an aim of finding out an effective way of solving antivirus of Hemorrhagic virus of carp completely.
    
    
    
    
    IN research of transgenic fish , Hu- α -IFN gene ( recombination gene) is cutdown and introduced into the nuclei of oocytes or cytoplasm of Grass carp at one-cell or two-cell stage via micyoinjection by Narashige micyoinjection apparatus . the recombination gene micyoinjected is 5nl DNA (about 106-107) into everyone oocytes or cytoplasm of Grass carp. There were 32197 oocytes of 12 series via micyoinjection and achived 12945 fries in 2000 year , By hatching and raising .Genomic DNA was extracted from Grass carp who were transformated in 1120 Grass carp presented postive reaction by blood . The transgenic Grass carp were detected by PCR , Southern blot. The results showed that PCR applify a 485 specific molecular band in 672 individuals, the rate of positive reaction is 60%, Southern blot result shows a strong signal in transgenic fish . It is concluded that Hu- α -IFN gene has been integrated and expression . It is also that foreign gene integrating position and copy number is different individuals , By ELIS
    A detecting , 23.5% transgenic fish' were detected Hu- α -IFN gene expression in all 672 transgenic fish , but Expression level of Hu-α -DFN is significant difference in different individuals and growth period.
    it is also conformed that transgenic Grass carp presented masculine in ELISA detecting have more resistivity than control Grass carp in inoculatived GCHV testing , the rate is 60-70% .
引文
1 倪达书,汪建国主编.草鱼生物学与疾病.北京:科学出版社,1999
    2 Palmiter R D,Brinster R L,Hammer R E.,et al.Dramatic growth of mice that develop from egga microinjected with meta Hothionein-growth hormone fusion genes. Nature, 1982,300:611-615
    3 Chourrout,D. et al., 1996.High efficiengcy gene transfer in rainbow trout by microinjection into egg cytoplasm. Aquaculture. 51:143-150
    4 Ozato, K. et al., 1986. Production of transgenic fish. Cell Differ. 19:237-244
    5 Brem, G. et al.,1998.Geng transfer in tilapia. Aquaculture,68:209-219
    6 Chen, T. T. Powers, D. A.,1990.Transgenic fish. TIBTECH. 8:219-225
    7 Gong, Z. Y., Vielkind, J.,Hew, C. L., (1991)Mol. Marine Biol. Biotech. 1:64-72
    8 White, J. R. et al., CN1154142A, C12N15/17,p5-7
    9 Zhu,Z. et al.,1985.Z. Angew Ichthyol. 1:31-34
    10 朱作言等,1986.科学通报,31:988-990
    11 张念慈,杨广智.草鱼出血病病毒在ZC-7901细胞株中的适应培养及其病毒培养物的某些生物学特性,鱼病简讯,1986,2:7-8
    12 中国科学院水生生物研究所病毒组,草鱼出血病病原的研究,水生生物学集刊,1978,6(3):321-330
    13 中国科学院水生生物研究所病毒组、武汉大学病毒研究所电镜室,草鱼出血病病原的研究Ⅱ.电镜观察,水生生物学集刊,1980,7(1):75-84
    14 中国科学院武汉病毒研究所、中国水产科学研究院长江水产研究所,草鱼出血病毒的电子显微镜观察出报,淡水渔业,1983,3:39
    15 中国科学院武汉病毒研究所、中国水产科学研究院长江水产研究所,草鱼出血病病原-鱼呼肠孤病毒(FRV)核酸特性研究,淡水渔业,1984,4:7-9
    16 中国科学院武汉病毒研究协作组,草鱼出血病病毒精细结构的研究,淡水渔业,1984,(2):21-22
    
    
    17 毛树坚、邵健忠,杭绮等.草鱼出血病的病原研究,水产学报,13(1):1-4
    18 毛树坚,杭绮,陈汉民等.草鱼出血病两种病原病毒的细胞病理学观察,海洋与湖沼,19(5):435-438
    19 卢全章,雷武.草鱼出血病组织病理学研究,鱼病简讯,(1):14-17
    20 卢全章.草鱼胸腺组织学的研究,水生生物学报,15(4):327-332
    21 卢全章,郭琼林.草鱼出血病胸腺组织病理的研究,,中国水产学会鱼病研究会第二次代表大会学术讨论会论文摘要汇篇,1989,:74-75
    22 叶雪平,杨广智,罗毅志.免疫酶染色快速检测草鱼出血病病毒抗原的方法,1989,16,第二次全国鱼病研究学术讨论会论文会刊.
    23 陈燕燊,江育林.草鱼出血病病毒形态结构及理化特性的研究,科学通报,1983,18:138-1140
    24 陈燕燊,刘建平,黄森.从草鱼亲鱼卵提纯的病毒电镜观察,全国草鱼病研究学术讨论会论文汇编,1984,23
    25 邵健忠,毛树坚,沈一雨.草鱼出血病两种病原病毒的分离和致病性的研究,杭州大学学报,1989,17(1):74-79
    26 闵淑琴,洪世雯,蔡宜权.鱼呼肠病毒(FRV)抗血清的制备及其应用,水产学报,1986,10(4):383-387
    27 郑德崇,黄琪琰,蔡完其等.草鱼出血病组织病理研究,水产学报,1986,10(2):151-159
    28 章怀云.肖调义.张学文,等.草鱼出血病病毒GcHv991理化性质研究[J].湖南农业大学学报,1991,25(3):350~356.
    29 Wolf, K., 1998,Fish Virus and Fish Virus Disease, 8: 65-68,Comstock Publishing Associates A Division of cornell University Ithaca and London.
    30 柯丽华,方勤,蔡宜权.一株新的草鱼出血病病毒分离物的特性[J].水生生物学报,1990,14(2):153~159
    31 Murphy F A, Fauquet C M, Bishop D H L et al. Virus Taxnomy [J]. Arc hives of Virology, 1995, (suppl): 208~239
    32 田静,邹桂平,方勤.草鱼出血病病毒基因组的cDNA合成、克隆及序列分析[J].
    
    中国病毒学,1999,14:87~92
    33 方勤,田静.草鱼呼肠孤病毒(GCRV)部分基因片段cDNA文库的构建,中国病毒学,2001,15:84~90
    34 何丽华,王伟,方勤等,1992.草鱼出血病病毒多肽及其基因组的体外翻译,病毒学报.8(2);169—173
    35 黄蹈,柯丽华.蔡宜权等、1992.草鱼出血病病毒的反转录活性的研究.病毒学报,8(1):50—56
    36 陈燕新。1991.草鱼出血病病毒RNA基因组的分析.鱼类病害研究,13(2);1-5
    37 Wang Tie-hui, Chen Hong-xi, Liu han-qin et al. 1994,Purification of hemorrhagic Virus of Grass carp and the cDNA synthesis、cloning and sequening of its Genome Annual Report of FEBL. Beijing. International Academic publishers, 153-156.
    38 Winton J R, Lanman C N, Fryer J L et al . 1987,Morphological and biochemical properties of a novel groupe of reovirous isolated from aquatic animals, J Gen Virol, 68:353-364
    39 方勤,肖调义,等.草鱼呼肠孤病毒991分离株的病毒学特性分析,中国病毒学,2002,17(2):178-181
    40 方勤,肖调义,李旅等.四株草鱼呼肠孤病毒毒株的细胞感染特性分析,中国病毒学,2002,17(2):182-184
    41 李军,王铁辉,陆仁后等,1996a.鱼类病毒检测技术.海洋与朔沼通报,2:58—65
    42 李军,王铁辉,陆仁后等,1996b,逆转录聚合酶链式反应中dsRNA模板的快速制备.青岛海洋大学学报,26(4):495—499
    43 杨广志,罗毅志,叶雪平,1991.葡萄球菌A蛋白协同凝集试验快速检测草鱼出血病病毒的研究.水产学报,15(1):27—33
    44 江育林,李艳,李正秋,1993.两种快速检测技术试验条件的探索及特性比较.中国水产学会色病学分会第三次鱼病研讨论会论文摘要汇编.武汉
    45 邵健忠,项黎新,李亚南等,1996.应用Dot-ELIsA技术检测草鱼出血病病毒的研究,水产学报.20[3];6-11
    
    
    46 李军,王铁辉,周立冉等,1997.应用RT—PCR技术对草鱼出血病病鱼组织的初步研究.水产学报,2[2]:175—179
    47 Li J, Wang T, Liu H et al. 1997, A detection method of hemorrhagic Virus of Grass carp (GCHV) based on the reverse transcription polymerase chain reaction Diseases of Aquatic Organisms, 29:7-12
    48 朱心玲,李爱华,射巧雄,1993.克列奥鱼服康抗草鱼出血病病毒的实验研究.见:鱼病学研究论文集,北京:海洋出版社.20—25
    49 王铁辉,陈宏溪,1995.草鱼出血病研究进展.见:彭珍荣等缩.现代微生物学研究进展.武汉:武汉大学出版社,150—159
    50 江育林.李正秋.1991.病毒感染的草鱼细胞产生类干扰素物资的研究.病毒学报,7:30—35
    51 邵健忠,项黎新,李亚南等,1993.从草鱼细胞分离到一种出血病病毒蛋白因子的研究.病毒学报,9(4):352—360
    52 Isaasc A Lindanmannj. Proc. Rou. Sco. B, 1957, 145: 258-267
    53 王明俊,等.兽医生物制品学,北京:中国农业出版社1999
    54 李雅林,等.干扰素的研究进展.预防兽医学进展,2001,3(2):40-43
    55 侯云德,吴淑华.干扰素[M].北京:人民出版社,1981
    56 Roberts R M, Liu L, Guo Q, et al. The evolution of the type Ⅰ interferons [J].J. interferon Cytokine Res, 1998,18:805-816
    57 Mogen K E, Lewerenz M, Reboul J, et al. The type Ⅰ interferon receptor : structure, function and evolution of a family bus [J]. J interferon Cytokine Res, 1999,19:1069-1098
    58 Sen G C, Ransohoff R M. Interferon-induced antiviral actions and their regulation [J]. Adv Virus Res, 1993,42:57-102
    59 Imada K, Leonard J W. The Jak-STAT pathway [J]. Molecular Immunology, 2000,37:1-11
    60 Ible J N. STATs: singal transducers and activators of transcripton [J]. Cell, 1996,84:331-334
    61 Takeda K, Kaisho T, Kaisho T, Yoshida N, et al. Stat 3 activation is responsible for
    
    IL-16-dependent T-cell proliferation through preventing apoptosis: generation and characterization of T cell-specific Stat 3-deficient mice [J]. J Immunol, 1998,161:4652-4660
    62 Starr R, Willson T A, Viney E M, et al. A family of cytokine-inducible inhibitors of signalling [J]. Nature, 1997,84:917-921
    63 Zhang X, Blenis J,Li H C,et al. Requirement of serine phosphphorylation for formation of STA-promoter complexes [J]. Science, 1995,267:1990-1994
    64 Cella N, Groner B,Hynes N E. Characterization of Stat5a and Stat5b homodimers and heterodimers and their association with the glucocorticoid receptor in mammary cells [J]. Mol Cell Biol, 1998,18:1783-1792
    65 郭良耀.干扰素及其临床应用.福建医药杂志.1991,13(1):39
    66 章怀云等.HuIFN-α对草鱼出血病毒干扰作用的研究,湖南师范大学自然科学学报.1993,16:104-107
    67 符少辉,陈韬,汪冬庚等.人IFN-α诱导草鱼肾细胞对草鱼出血病毒抗性作用的研究,水生生物学报,1999,23(3):290-292
    68 侯云德等.现代分子病毒学选论.北京,科学出版社,182-197,1994
    69 王秋娟等.家蚕细胞基因工程HuIFN-α注射液抗Ⅱ型单纯疱疹病毒作用,中国药科大学学报,1996,27(9):557-561
    70 Cella N, Groner B, Hynes N E.Characterization of Stat5a and Stat5b homodimers and heterodimers and their association with the glucocorticoid receptor in mammary cells[J]. Mol Cell Biod, 1998,18:1783-1792.
    71 Imada K, Bloom E T, Nakajima H, et al. Stat5b is essential for nature killer cell-mediated proflliferation and cytolytic activity[J]. J Exp Mdd, 1998,188:2067-2074.
    72 Kawata T, Shevchenko A, Fukuzawa M, et al. SH2 signaling in a lower eukaryote: a Stat protein that regulates stalk cell differentiation in Dictyostelium[J].Cell, 1997,89:909-916.
    73 Christian Bogdan, The function of type Ⅰ interferons in antimicrobial immunity[J], Current Opinion in Immunology, 2000,12:419-424.
    74 Imada K,Leonard J W. The Jak-STAT pathway[J].Molecular Immunology, 2002,37:1-11.
    
    
    75 Siegal P F, Kadowaki N, Shodell M, et al. The nature of the principal type Ⅰ interferon-producing cells in human blood[J]. Science, 1999,284:1835-1837.
    76 Takaoka A, Mitani Y, Suemori H, et al..Cross talk between interferon-y and a/b signalling components in caveolar membrane domains[J]. Science, 2000,288:2357-2360.
    77 Roberts R M, Liu L, Guo Q,et al .The type Ⅰ interferons [J] .J Interferon Cytokine Res, 1999,19:1069-1098
    78 Mogensen K E, Lewerenz M, Reboul J et al. The type Ⅰ interferon receptor: structure function and evolution of a family bus[J]. J Interferon Cytokine Res, 1999, 19: 1069-1098.
    79 萨姆布鲁克 J,弗立奇 E F,曼尼阿蒂斯 T,分子克隆指南.金冬雁,黎孟枫等译.第二版.北京:科学出版社,1998
    80 陈立祥,符少辉,汪冬庚等.草鱼出血病毒962毒株的生物学特性研究[J],湖南农业大学学报,1998,24(6):468-470
    81 许淑英,李焕林等.草鱼出血病细胞培养弱毒疫苗的制备及其免疫效果[J],水产学报,1994,18(2):110-117
    82 Liu Z, Moav B, Faras J A, et al. Molecular and cellular biology, 1990, 10(7): 3432
    83 杨隽,杨东亚,郭志光,孙秀英。全鱼基因在鲤鱼体内整合行为的研究。黑龙江八一农垦大学学报,1997,9(1):57-59
    84 Inoue k,,Akita N, Shiba T.,et al. Netal-inducible activities of metallothionein promoters in fish cells and fly.Biochem. Biophys. Res. Cmm, 1992,185:1108-1114
    85 Dunham R A, Eash J ,Askins J and Townes T M. Transrer of the metalltthiomein-human guowth hormone fusion gene into channel catfish. Trans. Am. Fish Soc, 1987,116:87-97
    86 Guyomard R, Chourrout D and Houdebine L M. Gene transfer by microinjection into fertilized trout eggs:efficient integration and germ line transmission. Abstr.3rd, Inrernational Symposium of Genetics in Aquaculture, 1988,20.Norway.
    87 G. Brem, B.Brenig, G. borstgen-Schwark et al. Gene Transfer m Tilapia (oreochromis niloticus) Aguaculture (1998,68:209~219)
    88 Shamloal A M, Hadidi A. Sensitive detection of potato Spindle tuber and temperate.
    
    from free Viwoids by reverse transcription polymerase chain reaction probe Capture hybridization[J].J Virol Meth, 1999,80:145~155.
    89 Zerbun M,,Gibellni D,Musam Musam M, et al. Autoated detection of digoxigemn labeled B19 Parvowous amphems by a Capture hybridization assay[J].J Virol Meth, 1995,55:1~7
    90 Dale P J;Senior I J. 1997.The possible impacts of multiple transgenes. Proceedings of the 1997 Brighton Conference 265~272.
    91 Harding K;Harris P S. 1994.Risk assessments of the release of genetically modified plants:a review. MAFF 54PP.
    92 Messean A. 1997. Management of herbicide tolerant crops in Europe. Proceeding of the 1997 Brighton Conference 947~954.
    93 Rogers H J;Matharu B;Parkes H C . 1996 Monitoring releases of transgenic Plants theoretical and Practical Considerations BCPC Symposium Proceedings of, 39~45.
    94 Rudelsheim P;Hugbrechts I.1996.A Case study of hybrid oilseed rape: from Conce ption to Marketing. Report of the 4th NIAB International Forum, Genetically Modified Corp Cultivars 10PP.
    95 薛达元IVar Virgin生物安全管理与实践—南京生物安全国际研讨会论文集,1998,中国南京,中国环境科学出版社.
    96 Charron,j.,Malynn, B.A.,Robertson, E.J.,Goff, S.P.,Alt, W.,High-frequence disruption of the N-myc gene in embryonic stem and pro-B cell lines by homologyus recombination, Mol. Cell. Biol., 1990.10:1799-1804
    97 Gorman, C.M.,Moffat,L.F., and Howard, B.H., Recombinant genomes which express chloramphenicol acetyi transferase in manmalian cells ,Mol. Cell.Biol., 1982,2:1044-1051
    98 Gu,H.,Zou,Y.R., Rajewsky, K., Independent control of immunoglobulin swith recombination at individual switch regions evidence through Cre-loxp-mediated gene targeting, Cell. Vol., 1993,73:1155-1164
    99 Hasty, R, Rivera-perez, J., Bradley, A.,The role and fate DNA ends for homolgous. recombination in embryonic stem cells ,Mol. Cell. Biol., 1992,12:2464-2474
    
    
    100 Penman, DJ., Beeching, A.J., Penn, S.and Maclean, N., Factors affection survial and integration following microinjection of novel DNA into rainbow trout eggs, Aquaculture, 1990,85:35-50
    101 Potter, H., Dressler, D., On the mechanism of genetic recombination :electron microscopic observation of recombination intermediates,Proc.Natl. Acad. Sci.USA, 1976, 73:3000-3004
    102 Stasiak, A., Thrtee-stranded DNA structure :is it the secret of DNA homologous recombination?, Mol.Microbio., 1992, 6: 3267-3276
    103 Zhu,Z., G.Li, L.He, S.Chen,Novel gene transfer into the eggs of goldfish(Carassius auratus L. 1758),Z. angew. Ichthyol., 1985,1:31-34
    104 Zhu, Z.,Generation of fast growing transgenic fish:Methods and mechanisms .,in Transgenic Fish. Hew, C.L. and Fletcher, G.L(eds),Word scientific publishing,Singapore, 1992a, pp.92-119
    105 Zhu,Z., Growth hormone gene and the transgenic fish:In Agricultural Biotechnology. You, CB. and Chen, Z.Z.(eds). China science and Technology Press,Beijing, 1992b,pp. 106-116
    106 Yoon, S.J., Hellerman, E.M., Gross, M.L.,Liu,Z., Schneider, A.J., Faras, A.J., Hackett,P.B., Kapuscinski, A.R. and Guise,K.S., Transfer of the gene for neomycin resistance into goldfish, Carassius auratus. Aquaculture. 1990,85:21-23
    107 Thomas, K.R., Folger, K.R., Capecchi,M.R., High frequency targeting of genes to specific sites in the manmalian genome, Cell, 1986,44:419-428
    108 Van Deursen, J.,Wiering,B., Targeting of the creatine kinase M gene in embryonic stem cells using isogenic and nonisogenic vectors,Nucl. Acids. Res., 1992,20:3815-3820
    109 Wang s.&Hazelrigg T., Tmplications for bed mRNA localization from soatial distribution of exu protein in Drosophila oogenesis, Nature, 1994,369:400-403
    110 Westhusin,M., From mighty mice to mighty cow, Nature genetics, 1997,17:4-5
    111 Sedivy, J.M., Joyner, A.L., Gene targeting ,in gene targeting ,Oxford University Press, Oxford, Ny., 1992,77-122
    
    
    112 Stuart, G.W., McMurray,j.V.,and Westerfield,M., Replication, integration and stable germline transmission of foreign sequences injected into early zebrafish embryos,Development.1988,103:403-412
    113 Schwartzberg, P.L.,Robertson,E.J.,Goff, S.P.,Targeted gene disruption of the endogenous c-abllocus by homologous recombination with encoding a selectable fusion protein,Proc. Natl. Acad. Sci. USA, 1990,87:3210-3214
    114 Satyabhama, S.,Alan, L., Short-term efficient express of transfected DNA inj huan hematopoietic cells by electroporation:Definition of parameters and use of chemical stimulators,DNA, Mary ann Liebert,INC.,publishers,1988,7(3):203-209
    115 Liskayu,R.M.,Letson,A.,Stachelet,J.L.Homology requirement for efficient gene conversion between duplicated chromosomal sequences in mammalian cells, genetics, 1987,115:161-167
    116 Cui,Z., Zhu,Z., Cui,Y., Li, G. And Xu,K., Food consumption and enery budget in MThGh-transgentic F2 red carp (Cyprinus carpio L. Red var.).Chinese science Bulletin, 1996,41:591-596
    117 Duguay, S.J., Park, L.K.,Saadpour, M., and Dickhoff, W.W. Nucleotide sequence and tissue distribution of three insulin-like growth factor Ⅰ prohormones in salmon, Mol. Endocrinol, 6:1202-1210
    118 谢岳峰,朱作言.鱼类受精卵基因转移中的剂量效应,中国鱼类协会第三届会员代表大会及学术讨论会论文摘要汇编,1989,33-34
    119 邹钧、刘东,谢岳峰,朱作言。外源基因在鱼为胚胎发育过程中的发达。水生生物学报,1991,15(4):372-374
    120 朱作言,许克圣,谢岳峰等,转基因鱼模型的建立.中国科学,1989,B(2):147-155.
    121 Cui,Z.andZhu, Z., Hormonal replacement therapy in fish:human growth hormone gene unctionin hypophysectiomized carp,Fish Physiology and Biochemistry, 1993,12(2): 161-169
    122 Donaldson,E.M. and Hunter, G.A.,The Ocean release and contribution to the fishery of aa-female and sterile group of coho samon (oncorhynchus kisutch),In:Reproductive
    
    physiology of fish (eds. Richter C J J and Goos H J Th),p.78,wageningen, 1982
    123 Dumham,KA.,Eash, J.,Askins,J. And Townes, T.M., 1987.Transfer of the metallothionein human growth horone usion gene into channel catfish, Trans. Am. Fish. Soc. 116:87-91
    124 Devlin, R.,Yesaki, T.Y.,Blag,C.A.,Donaldson,E.,M.,Swanson, P. And Chan, W.,Extraordinary Salnon growth, Nature, 1994,371:209-210.
    125 夏德全,吴婷婷,杨弘等.人生长激素基因在团头鲂和鲤中的整合和表达.水产学报,1994,18(4):284—289.
    126 魏彦章,许克圣,俞豪祥,牛生长激素基因向“缩骨鲫”受精卵转移的初步研究.水产科技情报,1990,17(4):100-103
    127 孙孝文,梁利群,沈俊宝,全鱼基因工程鱼的构建.高技术通讯,1993,3(9):23—26.
    128 Mark L G, et al. Aquacultue,1992,103:253-273.
    129 龙华,尾里建二郎,若松佑子等.红色荧光蛋白(PEP)在转基因青鱼将中的表达.中国水产科学.2002,(2):97-99
    130 陈兰英,方福德.转基因研究的现状[J].生命的化学,1996,16(1):7-9
    131 Shigeru Takagi Sasado,Gen Tamiya, et al. An efficient expression vector for transgenic medaka construction [J].Mole Mar Biol,1994,3 (4): 192-199
    132 Tsai Huai-Jen, Wang Shu-huei,Koji Inoue, et al. Initiation of the transgenic lacZ gene expression in Medaka (Oryzias latipes)embryos[J].Molec Mar Biol Biot,1995,4(1):1-9
    133 汪亚平,胡炜,冯建新等,转“全鱼”生长激素基因鲤鱼及其F_1遗传分析,科学通报,2001,46(3):226-229

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700