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HLA-Ⅱ类基因DR_α及DRB_1 0401转基因小鼠模型的遗传与繁殖 被引量:1

Breeding and Genetic of HLA-DRα,DRB_1 0401 Transgenic Mice Model
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摘要 采用类系祖建系的方法 ,对HLA -Ⅱ类基因DRα 和DRB1   0 4 0 1转基因小鼠模型进行了繁育。通过PCR和Southernblot分子杂交的方法 ,检测小鼠尾组织的DNA样品 ,以确定DR基因的整合和复制情况。结果表明 ,HLA -Ⅱ类基因DR已稳定地遗传至第五代(F5) ;共产仔 32 6只 ,PCR检测出阳性小鼠 95只 ,阳性率为 2 9.1 %。PCR—Southern印迹杂交检测 ,发现 68只仔鼠整合有DR基因 ,总有效率为 2 0 9%。经Nothern杂交和RT -PCR检测HLA -DR基因在脾脏和肾脏中均有表达。 s We have constructed transgenic mice Model on DRα and DRB 1 *0401 of MHC-II molecules by microinjected techniques on germ nucleus of zygotes, DRα and DRB 10401 genes were microinjected into the fertilized eggs of C57BL/6×DBA/1 hybrid mice and transplanted into the oviducts of pseudopregnancy female mice. The total integration rate and efficient rate of transgene were 29.1% and 20.9% assessed by PCR, Southern blot, Northern blot and RT-PCR analysis.There were 5 founders of all injected mice, which had steadily inherited to the fifth generation. It was found that 95 mice were positive by PCR and 68 mice were integrated exogenouse gene by Southern blot analysis DR α and DRB 1 *0401 gene were experssed on spleen and kidney of transgenic mice. This experiment on the breeding and genetic of DRα and DRB 1 *0401 transgenic model is a success.
出处 《中国实验动物学报》 CAS CSCD 2000年第1期36-40,共5页 Acta Laboratorium Animalis Scientia Sinica
基金 国家自然科学基金!资助课题 编号 3 93 70 865
关键词 HLA-Ⅱ类基因 HLA-DR基因 转基因小鼠模型 总有效率 阳性 仔鼠 脾脏 遗传 产仔 繁殖 HLA-DR4 gene Transgenic mice model Gene intergration Breed system
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  • 1Wood,A.Hychen,METambauer,Aetal.HumanMHCclass-restrictedTcellReasponseintransgenicmice,JExpMed1994,180∶173
  • 2Yamamnoto,K.FuKui,YEaski,Tetal.FunctionalinreactionbetweenHLAclass-ⅡandmouseCD4MoleculesinAntigenrecognitionbyTcellsinHLA-DRandDQtransgenicJExpMED1994,180∶165
  • 3FuKamizu,A,etal.J.Bid,RegulatorsandHomeostaticAgents,1991,5∶112-116
  • 4邓军卫,吴轰,游学科,冯清泉,李芬,朱亚辉,卢光琇.HLA-Ⅱ类基因DR_α、DRB_1*0401转基因鼠模型的建立及体内表达研究[J].中华医学遗传学杂志,1999,16(6):360-363. 被引量:3
  • 5Gorden,JWetal.GenetictransformationofmouseembryosbymicroinjectionofpurificationDNAProc,Natlacadsci2980,77∶7380
  • 6White,B.A.PCRProtocols,CurrentMethodsandApplication,HumanPressInc,Totowa,NewJersey1993
  • 7杜立新.动物基因转移的方法、问题与应用前景[J].草食家畜,1994(4):17-19. 被引量:1

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  • 1赵义,向志光,陈振军,张连峰,栗占国.HLA-DRα和HLA-DRB1^*0405表达载体的构建及其在真核细胞中的表达[J].中国比较医学杂志,2007,17(6):311-316. 被引量:2
  • 2Touloukian CE, Leitner WW, Topalian SL, et al. Identification of a MHC class Ⅱ-restricted human gp100 epitope using DR4-IE transgenic mice[J]. J Immunol, 2000, 164:3535- 3542.
  • 3Rosloniec EF, Brand DD, Myers LK, et al. Induction of autoimmane arthritis in HLA-DR4 (DRB1 * 0401 ) transgenic mice by immunization with human and bovine type Ⅱ collagen [ J ]. J Immunol, 1998, 160:2573-2578.
  • 4Wang D, Hill JA, Jevnikar AM, et al. Induction of transient arthritis by the adoptive transfer of a collagen Ⅱ specific Th1 clone to HLA- DR4 (B1 * 0401) transgenic mice[J]. J Autoimmun, 2002, 19:37-43
  • 5Myers LK, Sakurai Y, Tang B, et al. Peptide-induced suppression of collagen-induced arthritis in HLA-DR1 transgenic mice[J]. Arthritis Rheum, 2002, 46:3369 - 3377.
  • 6Sakurai Y, Brand DD, Tang B, et al. Analog peptides of type Ⅱ collagen can suppress arthritis in HLA-DR4 (DRB1 * 0401 ) transgenic mice[J]. Arthritis Res Ther, 2006, 8:R150.
  • 7Zanelli E, Gonzalez-Gay MA, David CS. Could HLA-DRB1 be the protective locus in rheumatoid arthritis? [J]. Immunol Today, 1995, 16:274 - 278.
  • 8Nabozny GH, Baisch JM, Cheng S, et al. HLA-DQ8 transgenic mice are highly susceptible to collagen-induced arthritis: a novel model for human polyarthritis[J]. J Exp Med, 1996, 183:27 - 37.
  • 9Bradley DS, Nabozny GH, Cheng S, et al. HLA-DQB1 polymorphism determines incidence, onset, and severity of collageninduced arthritis in transgenic mice. Implications in human rheumatoid arthritis[J]. J Clin Invest, 1997, 100:2227- 2234.
  • 10Taneja V, Griffiths MM, Luthra H, et al. Modulation of HLA-DQrestricted collagen-induced arthritis by HLA-DRB1 polymorphism [J]. Int Immunol, 1998, 10:1449-1457.

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