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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >BINARY TRANSGENIC MOUSE MODEL FOR STUDYING THE TRANS CONTROL OF GLOBIN GENE SWITCHING - EVIDENCE THAT GATA-1 IS AN IN VIVO REPRESSOR OF HUMAN EPSILON GENE EXPRESSION
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BINARY TRANSGENIC MOUSE MODEL FOR STUDYING THE TRANS CONTROL OF GLOBIN GENE SWITCHING - EVIDENCE THAT GATA-1 IS AN IN VIVO REPRESSOR OF HUMAN EPSILON GENE EXPRESSION

机译:研究球蛋白基因转换的跨控制的二元转基因小鼠模型-证据表明GATA-1是人ε基因表达的体内抑制子。

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摘要

To test whether human GATA-1 (hGATA-1) is involved in the transcriptional control of globin gene switching, we produced transgenic mice overexpressing hGATA-1, crossed them with mice carrying a human beta-globin locus yeast artificial chromosome (beta YAC), and analyzed globin gene expression in their progeny, Mice carrying both the hGATA-1 and the beta YAC transgenes had normal levels of gamma- and beta-globin mRNA and no distortion in the rate or in the timing of gamma-to-beta switch, indicating that hGATA-1 is not involved in the developmental control of gamma- and beta-globin genes. In contrast, mice carrying the hGATA-1 and the beta YAC transgenes had 5- to 6-fold lower expression of the human epsilon globin gene compared with beta YAC mice lacking the hGATA-1 transgene, These results provide direct in vivo evidence that hGATA-1 is a specific repressor of human epsilon gene expression, Our findings also suggest that binary transgenic mouse systems based on overexpression of transcriptional factors can be used to investigate the trans control of human globin gene switching, Systems as the one we describe here should be useful in the study of any developmentally controlled human gene for which transgenic mice are available. [References: 30]
机译:为了测试人类GATA-1(hGATA-1)是否参与球蛋白基因转换的转录控制,我们生产了过表达hGATA-1的转基因小鼠,将它们与携带人β-球蛋白基因座酵母人工染色体(beta YAC)的小鼠杂交,并分析了其子代中的球蛋白基因表达,携带hGATA-1和βYAC转基因的小鼠的γ-和β-球蛋白mRNA正常水平,且在γ到β转换的速率或时间上没有畸变,表明hGATA-1不参与γ和β珠蛋白基因的发育控制。相反,与没有hGATA-1转基因的βYAC小鼠相比,携带hGATA-1和βYAC转基因的小鼠的人ε珠蛋白基因表达降低了5至6倍。这些结果提供了直接的体内证据,证明hGATA -1是人类epsilon基因表达的特异性阻遏物,我们的发现还表明,基于转录因子过度表达的二元转基因小鼠系统可用于研究人类球蛋白基因转换的反式控制。可用于研究任何可获得转基因小鼠的受发育控制的人类基因。 [参考:30]

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