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Stable expression of a heterogeneous gene introduced via gene targeting into the HPRT locus of human fibrosarcoma cells

机译:通过基因靶向导入人纤维肉瘤细胞HPRT基因座的异质基因的稳定表达

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To obtain a cell line that maintains stability of gene expression is important for industrial production of therapeutic proteins from recombinant cells. In this study, we attempted to improve the stability of expression of an exogenous gene by using the gene-targeting method in cultured cells. In our gene-targeting system, the green fluorescent protein (GFP) gene was used as an exogenous reporter gene targeted to the locus of the endogenous hypoxanthine phosphoribosyl transferase (HPRT) gene, which is constitutively expressed. Cell lines selected using markers of the targeting DNA were cultivated for 129 days without any drug selection, and the expression levels of GFP protein and the chromosomal structure of the gfp gene in these cell lines were evaluated. Cell lines in which gfp genes were randomly integrated into the genome showed decreased GFP expression, which resulted from loss of genes or attenuation of transcription. In contrast, cell lines in which the gfp gene was targeted to the hprt locus maintained a stable chromosomal structure and stable expression of the gfp gene, even after prolonged cultivation. These results suggest that constitutively expressed endogenous gene loci may be suitable positions for stable expression of exogenous genes, and that the gene-targeting strategy presented here may be useful for generation of cell lines for industrial protein production. (c) 2006 Wiley Periodicals, Inc.
机译:获得维持基因表达稳定性的细胞系对于从重组细胞工业生产治疗性蛋白质是重要的。在这项研究中,我们试图通过在培养细胞中使用基因靶向方法来提高外源基因表达的稳定性。在我们的基因靶向系统中,绿色荧光蛋白(GFP)基因用作外源报道基因,靶向组成型表达的内源性次黄嘌呤磷酸核糖基转移酶(HPRT)基因的基因座。在不进行任何药物选择的情况下,将使用靶向DNA的标记物选择的细胞系培养129天,并评估了这些细胞系中GFP蛋白的表达水平和gfp基因的染色体结构。 gfp基因随机整合到基因组中的细胞系显示GFP表达下降,这是由于基因丢失或转录减弱所致。相反,即使长期培养,其中将gfp基因靶向hprt基因座的细胞系仍保持稳定的染色体结构和gfp基因的稳定表达。这些结果表明,组成性表达的内源基因位点可能是外源基因稳定表达的合适位置,并且此处介绍的基因靶向策略可能对生产工业蛋白质的细胞系有用。 (c)2006年Wiley Periodicals,Inc.

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