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Targeting of human eNOS promoter to the Hprt locus of mice leads to tissue-restricted transgene expression

机译:将人eNOS启动子靶向小鼠的Hprt基因座导致组织限制性转基因表达

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摘要

Phenotypic heterogeneity of the endothelium arises from cell type-specific differences in gene expression. An understanding of the mechanisms that underlie differential gene expression would provide important insight into the molecular basis of vascular diversity. In standard transgenic assays, multiple copies of heterologous DNA cassettes are randomly integrated into the mouse genome, resulting in significant line-to-line variation in expression. To overcome these limitations, we have targeted a single copy of a transgene that contains 1,600 bp of the human endothelial nitric oxide synthase (eNOS) promoter coupled to the LacZ reporter gene to the X-linked hypoxanthine phosphoribosyltransferase (Hprt) locus of mice by homologous recombination. The transgene was inserted in either of the orientations relative to that of the Hprt gene. In mice derived from multiple embryonic stem (ES) cell clones, the expression pattern was limited to a subset of endothelial cells, cardiomyocytes, and vascular smooth muscle cells. These findings suggest that Hprt locus targeting is a feasible tool for studying endothelial cell-restricted gene regulation.
机译:内皮的表型异质性来自基因表达中细胞类型特异性的差异。对差异基因表达基础的机制的了解将提供重要的洞察血管多样性的分子基础。在标准的转基因测定中,异源DNA盒的多个副本被随机整合到小鼠基因组中,从而导致表达的显着行间差异。为克服这些限制,我们已将含有1600 bp的人类内皮型一氧化氮合酶(eNOS)启动子与LacZ报告基因偶联的转基因的单个拷贝靶向小鼠的X连锁次黄嘌呤磷酸核糖基转移酶(Hprt)基因座。重组。以相对于Hprt基因的任一方向插入转基因。在源自多个胚胎干(ES)细胞克隆的小鼠中,表达模式仅限于内皮细胞,心肌细胞和血管平滑肌细胞的子集。这些发现表明,Hprt基因座靶向是研究内皮细胞限制性基因调控的可行工具。

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