期刊文献+

肝脏高效表达调控元件的构建及其表达效果的鉴定 被引量:2

Construction of a liver highly-effective control element and evaluation of its expression efficacy
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摘要 目的:构建一种肝脏高效表达调控元件,促进水动力转染外源基因在体内的长期高效表达。方法:构建了以hAAT基因作为报告基因,分别含有表达调控元件AerApoEAATP、ApoEAATP、A lbEAATP及CMV启动子的真核表达载体pC Ineo-AerApoEAATP-hAAT、pC Ineo-ApoEAATP-hAAT、pC Ineo-A lbEAATP-hAAT及pC Ineo-hAAT,水动力转染法将上述质粒分别转染BALB/c小鼠,定期检测小鼠血清中hAAT的浓度反应AerApoEAATP、ApoEAATP、A l-bEAATP及CMV的调控能力。结果与结论:所构建的表达调控元件AerApoEAATP具有较强的调控能力,其长期的调控水平高于CMV、A lbEAATP和ApoEAATP。 Objective: To construct a liver highly-effective control element that can prolong the expression time of hydrodynamically transfected gene. Methods: Plasmid pCIneo-AerApoEAATP-hAAT, pCIneo-ApoEAATP-hAAT, pCIneo-Al- bEAATP-hAAT and pCIneo hAAT were constructed respectively. All of them included hAAT gene as the reporter gene. BALB/c mice were transfected with the plasmids by hydrodynamical transfection technology. The activity of AerApoEAATP, ApoEAATP,AlbEAATP and CMV was compared by the concentration of hAAT. Results and Conclusion: The control element constructed is much stronger than ApoEAATP,AlbEAATP and CMV in the long-term expression.
出处 《军事医学科学院院刊》 CSCD 北大核心 2006年第3期206-208,229,共4页 Bulletin of the Academy of Military Medical Sciences
基金 国家自然科学基金 北京市自然科学基金资助项目(30300184 30400561 7063086)
关键词 BALB/C小鼠 Α1-抗胰蛋白酶 白蛋白 基因表达调控 BALB/c mice α1 - antitrypsin albumin gene expression regulation liver
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参考文献6

  • 1贾帅争,王全立.水动力转染基因在小鼠体内的长期高效表达[J].生物技术通讯,2005,16(3):307-309. 被引量:6
  • 2Kramer MG,Barajas M,Razquin N,et al.In vitro and in vivo comparative study of chimeric liver-specific promoters.[J].Mol Ther,2003,7(3):375-385.
  • 3Olivares EC,Hollis RP,Chalberg TW,et al.Site-specific genomic integration produces therapeutic factor Ⅸ levels in mice.[J].Nat Biotechnol,2002,20(11):1124-1128.
  • 4Miao CH,Ohashi K,Patijn GA,et al.Inclusion of the hepatic locus control region,an intron,and untranslated region increases and stabilizes hepatic factor Ⅸ gene expression in vivo but not in vitro[J].Mol Ther,2000,1(6):522-532.
  • 5Zhang G,Song YK,Liu D.Long-term expression of human alpha-1-antitrypsin gene in mouse liver achieved by intravenous administration of plasmid DNA using a hydrodynamics-based procedure[J].Gene Ther,2000,7(15):1344-1349.
  • 6Song S,Morgan M,Ellis T,et al.Sustained secretion of human alpha-1-antitrypsin from murine muscle transduced with adeno-associated virus vectors.[J].Proc Natl Acad Sci USA,1998,95(24):14384-14388.

二级参考文献18

  • 1Liu F,Song Y,Liu D. Hydrodynamics-based transfection in animals by systemic administration of plasmid DNA [J].Gene Ther,1999,6(7): 1258.
  • 2Zhang G,Gao X,Song YK,et al.Hlydroporation as the mechanism of hydrodynamic deliverv[Jl.Gene Ther,2004,11(8):675.
  • 3胡锦辉 贾帅争 王全立.水动力转染技术及应用[J].国外医学分子生物学分册,2003,25:72-72.
  • 4Zhang G,Song YK,Liu D.Long-term expression of human alphal-antitrypsin gene in mouse liver achieved by intravenous administration of plasmid DNA using a hydrodynamics-based procedure[J].Gene Ther,2000,7(15):1344.
  • 5Yang J,Chen S,Huang L,et al.Sustained expression of naked plasmid DNA encoding hepatocyte growth factor in mice promotes liver and overall body growth[J].Hepatology,2001,33(4):848.
  • 6Kramer MG,Barajas M,Razquin N,et al.In vitro and in vivo comparative study of chimeric liver-specific promoters[J]. Mol Ther,2003, 7(3):375.
  • 7Miao CH,Ohashi K,Patijn GA,et al.Inclusion of the hepatic locus control region, an intron, and untranslated region increases and stabilizes hepatic factor IX gene expression in vivo but not in vitro[J].Mol Ther,2000,1(6):522.
  • 8Alino SF,Crespo A,Dasi F.Long-term therapeutic levels of human alpha-1 antitrypsin in plasma after hydrodynamic injection of nonviral DNA[J].Gene Ther,2003,10(19):1672.
  • 9Sclimenti CR,Neviaser AS,Baba EJ,et al.Epstein-Barr virus vectors provide prolonged robust factor IX expression in mice [J].Biotechnol Prog,2003,19(1):144.
  • 10Stoll SM,Sclimenti CR,Baba E J,et al.Epstein-Barr virus/humanvect or provides high-level,long-term expression of alphal-antitrypsin in mice[J].Mol Ther,2001,4(2):122.

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  • 1Alter M J, Mast E E. The epidemiology of viral hepatitis in the United States [J]. Gastroenterol Clin North Am, 1994,23: 437-455.
  • 2Cohen J. The scientific challenge of hepatitis C[J]. Science, 1999,285(5424):26-30.
  • 3De Francesco R, Steinkuhler C. Structure and function of the hepatitis C virus NS3-NS4A serine proteinase[J]. Curr Top Microbiol Immunol, 2000,242:149-169.
  • 4Foy E, Li K, Wang C, et al. Regulation of interferon regulatory factor-3 by the hepatitis C virus serine protease [J]. Sci- ence, 2003,300(5622):1145-1148.
  • 5Watashi K, Hijikata M, Tagawa A, et al. Modulation of retinoid signaling by a cytoplasmic viral protein via sequestra- tion of Sp110b, a potent transcriptional corepressor of RAR, from the nucleus[J]. Mol Cell Biol, 2003,23:7498-7509.
  • 6Yoshida T, Hanada T, Tokuhisa T, et al. Activation of STAT3 by the hepatitis C virus core protein leads to cellular transfor- mation[J]. J Exp Med, 2002,196:641-653.
  • 7Moriya K, Fujie H, Shintani Y, et al. The core protein of hepatitis C virus induces hepatocellular carcinoma in transgenic mice[J]. Nat Med, 1998,4:1065-1067.
  • 8lshikawa T, Shibuya K, Yasui K, et al. Expression of hepatitis C virus core protein associated with malignant lymphoma in transgenic mice[J]. Comp Immuno Microbiol Infec Dis, 2003,26: 115-124.
  • 9Meehyein K, Duckhyang S, Mahnhoon P, et al. Inhibition of hepatitis C virus gene expression by small interfering RNAs using a tri-cistronic full-length viral replicon and a transient mouse model[J]. Virus Res, 2006,122:1-10.
  • 10Wang LC, Fu QX, Zhan LS, et al. Bioluminescence imaging of Hepatitis C virus NS3/4 serine protease activity in cells and living animals[J]. Antiviral Res, 2010, 8(7): 50-56.

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