Construction and identification of transgenic porcine embryonic fibroblasts expressing epithelium-specific N-LMP1 and CR2
  • Article
  • | |
  • Metrics
  • |
  • Reference [25]
  • | | | |
  • Comments
    Abstract:

    Objective To construct an eukaryotic expression vector and identify the integration of nasopharyngeal carcinoma-derived oncogene latent membrane protein 1 (N-LMP1) and CR2 gene in porcine embryonic fibroblasts, and to provide a basis for construction of EBV-infection associated swine nasopharyngeal carcinoma model.Methods ED-L2 and N-LMP1 were synthesized directly. CR2 was amplified by RT-PCR from human B lymphocytes. The three fragments mentioned above were subcloned one by one into the eukaryotic expression vector pN1, and then the vector was transfected into porcine embryonic fibroblasts using the liposome reagent, according to the manufacturer's protocol. The cells were selected with G418 antibiotic and identified by PCR amplification. Results N-LMP1 and CR2 epithelium-specific expression vector was successfully constructed and integrated into the genome of the porcine fibroblasts, and clone cells integrating the N-LMP1 and the CR2 genes were obtained. Conclusions The porcine fibroblast clones integrating N-LMP1 and CR2 are obtained and they should be of great value for the construction of N-LMP1 and CR2 transgenic swine via cell nuclear transfer.

    Reference
    [1] Chodosh J, Gan Y, Holder VP, et al. Patterned entry and egress by Epstein-Barr virus in polarized CR2-positive epithelial cells[J]. Virology, 2000, 266(2):387-396.
    [2] Nemerow GR, Moore MD, Cooper NR. Structure and function of the B-lymphocyte Epstein-Barr virus/C3d receptor[J]. Adv Cancer Res, 1990, 54:273-300.
    [3] Frade R, Barel M, Ehlin-Henriksson B, et al. gp140, the C3d receptor of human B lymphocytes, is also the Epstein-Barr virus receptor[J]. Proc Natl Acad Sci U S A, 1985, 82(5):1490-1493.
    [4] Volsky DJ, Shapiro IM, Klein G. Transfer of Epstein-Barr virus receptors to receptor-negative cells permits virus penetration and antigen expression[J]. Proc Natl Acad Sci U S A, 1980, 77(9):5453-5457.
    [5] Li QX, Young LS, Niedobitek G, et al. Epstein-Barr virus infection and replication in a human epithelial cell system[J]. Nature, 1992, 356(6367):347-350.
    [6] 纪志武, 李保民, 曾毅. 采用病毒受体基因转移技术建立EB病毒细胞感染模型[J]. 病毒学报, 1994, 10(2):154-158.
    [7] Fingeroth JD, Diamond ME, Sage DR, et al. CD21-Dependent infection of an epithelial cell line, 293, by Epstein-Barr virus[J]. J Virol, 1999, 73(3):2115-2125.
    [8] Hu LF, Zabarovsky ER, Chen F, et al. Isolation and sequencing of the Epstein-Barr virus BNLF-1 gene (LMP1) from a Chinese nasopharyngeal carcinoma[J]. J Gen Virol, 1991, 72 (Pt 10):2399-2409.
    [9] Hu LF, Chen F, Zheng X, et al. Clonability and tumorigenicity of human epithelial cells expressing the EBV encoded membrane protein LMP1[J]. Oncogene, 1993, 8(6):1575-1583.
    [10] Li SN, Chang YS, Liu ST. Effect of a 10-amino acid deletion on the oncogenic activity of latent membrane protein 1 of Epstein-Barr virus[J]. Oncogene,1996, 12(10):2129-2135.
    [11] Nakagawa H, Wang TC, Zukerberg L, et al. The targeting of the cyclin D1 oncogene by an Epstein-Barr virus promoter in transgenic mice causes dysplasia in the tongue, esophagus and forestomach[J]. Oncogene, 1997, 14(10):1185-1190.
    [12] 蓝轲, 乔贵林, 沈新民, 等. 鼻咽癌来源潜伏膜蛋白1的表达诱发转基因小鼠鼻咽不典型增生[J]. 动物医学进展, 2002, 23(5):46-48.
    [13] 王桂花, 尹晓敏, 孙霞, 等. 国内外小型猪资源概况[J]. 中国比较医学杂志, 2009, 19(2): 71-73.
    [14] Dinnyes A, De Sousa P, King T, et al. Somatic cell nuclear transfer: recent progress and challenges[J]. Cloning Stem Cells, 2002, 4(1):81-90.
    [15] 魏庆信, 郑新民, 赵浩斌, 等. 转基因猪研究进展[J]. 中国比较医学杂志, 2005, 15(2):112-115.
    [16] Umeyama K, Watanabe M, Saito H, et al. Dominant-negative mutant hepatocyte nuclear factor 1alpha induces diabetes in transgenic-cloned pigs[J]. Transgenic Res, 2009, 18(5):697-706.
    [17] Yang D, Yang H, Li W, et al. Generation of PPARgamma mono-allelic knockout pigs via zinc-finger nucleases and nuclear transfer cloning[J]. Cell Res, 2011, 21(6):979-982.
    [18] 陈华. 小型猪动脉粥样硬化模型[J]. 中国实验动物学报, 2008, 16(5):376-380.
    [19] Kragh PM, Nielsen AL, Li J, et al. Hemizygous minipigs produced by random gene insertion and handmade cloning express the Alzheimer's disease-causing dominant mutation APPsw[J]. Transgenic Res, 2009, 18(4):545-558.
    [20] 俞远京. 转基因克隆猪与人类异种器官移植[J]. 中国比较医学杂志, 2004, 14(1):50-53.
    [21] Wang J, Wang W, Li R, et al. The diploid genome sequence of an Asian individual[J]. Nature, 2008, 456(7218):60-65
    [22] Johnson RJ, Stack M, Hazlewood SA, et al. The 30-base-pair deletion in Chinese variants of the Epstein-Barr virus LMP1 gene is not the major effector of functional differences between variant LMP1 genes in human lymphocytes[J]. J Virol, 1998, 72(5):4038-4048.
    [23] Miller WE, Cheshire JL, Baldwin AJ, et al. The NPC derived C15 LMP1 protein confers enhanced activation of NF-kappa B and induction of the EGFR in epithelial cells[J]. Oncogene, 1998, 16(14):1869-1877.
    [24] Trivedi P, Hu LF, Chen F, et al. Epstein-Barr virus (EBV)-encoded membrane protein LMP1 from a nasopharyngeal carcinoma is non-immunogenic in a murine model system, in contrast to a B cell-derived homologue[J]. Eur J Cancer, 1994, 30A(1):84-88.
    [25] Nemerow GR, Houghten RA, Moore MD, et al. Identification of an epitope in the major envelope protein of Epstein-Barr virus that mediates viral binding to the B lymphocyte EBV receptor (CR2)[J]. Cell, 1989, 56(3):369-377.
    Related
    Cited by
    Comments
    Comments
    分享到微博
    Submit
Get Citation
Share
Article Metrics
  • Abstract:2520
  • PDF: 1758
  • HTML: 0
  • Cited by: 0
History
  • Revised:November 19,2013
  • Online: February 28,2014
Article QR Code