首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >High-level erythroid expression of human alpha-globin genes in transgenic mice.
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High-level erythroid expression of human alpha-globin genes in transgenic mice.

机译:人α-珠蛋白基因在转基因小鼠中的高水平红系表达。

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摘要

The human alpha 1-globin gene was fused downstream of two erythroid-specific DNase I super-hypersensitive sites that are normally located upstream of the human beta-globin locus. This construct was injected into fertilized mouse eggs, and expression was analyzed in 16-day fetal livers and brains. All 11 fetuses that contained intact copies of the transgene expressed correctly initiated human alpha-globin mRNA in the erythroid fetal liver but not in brain. Levels of expression ranged from 4% to 337% of endogenous mouse beta-globin mRNA. A human alpha-globin construct that did not contain super-hypersensitive sites was not expressed. These results demonstrate that human beta-globin locus activation sequences can stimulate high levels of human alpha-globin gene expression in erythroid tissue of transgenic mice. The results also provide a foundation for experiments designed to coexpress human alpha- and beta-globin genes in transgenic mice and suggest a feasible approach for production of a mouse model for human sickle cell disease.
机译:人α1珠蛋白基因融合在两个通常位于人β珠蛋白基因座上游的红系特异性DNase I超敏位点的下游。将该构建体注射到受精的小鼠卵中,并在16天的胎儿肝脏和大脑中分析其表达。包含完整转基因拷贝的所有11个胎儿均正确表达了在红系胎儿肝脏中而非人脑中的人α-珠蛋白mRNA。表达水平为内源性小鼠β-珠蛋白mRNA的4%至337%。没有表达不包含超敏位点的人α-珠蛋白构建体。这些结果证明,人β-球蛋白基因座激活序列可以刺激转基因小鼠红系组织中高水平的人α-球蛋白基因表达。该结果也为旨在在转基因小鼠中共表达人α-和β-珠蛋白基因的实验提供了基础,并提出了生产人镰刀细胞疾病小鼠模型的可行方法。

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