Regulation of human globin gene expression in mouse erythroleukemia x human fibroblast hybrid cells.

D Vembu, N S Young, M Willing, E Church, L Sanders-Haigh, W F Anderson
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引用次数: 5

Abstract

A somatic cell hybrid, XX-8, was obtained from a fusion of tetraploid mouse erythroleukemia cells with human Lesch-Nyhan skin fibroblasts. This hybrid cell was previously shown (1) to produce human beta- but no human gamma-globin mRNA sequences after induction with dimethylsulfoxide. In this study we show that: (a) human beta- and gamma-globin genes are present in XX-8 cells in approximately equal numbers; (b) no human gamma-globin mRNA sequences can be detected in either the cytoplasmic or nuclear RNA fractions even with several different inducers; (c) after induction the human beta-globin gene is converted from a DNase I insensitive or closed structure to a DNase I open configuration, while the human gamma-globin gene remains closed; and (d) no human beta-globin polypeptide can be detected in the intact induced cells, indicating that fibroblast globin genes, even when induced to make mRNA in an erythroid environment, do not synthesize an RNA that is translated efficiently.

人珠蛋白基因在小鼠红细胞白血病与人成纤维细胞杂交细胞中的表达调控。
从四倍体小鼠红白血病细胞与人Lesch-Nyhan皮肤成纤维细胞融合获得体细胞杂交XX-8。这种杂交细胞在二甲亚砜诱导后产生了人β -但没有产生人γ -珠蛋白mRNA序列。在这项研究中,我们表明:(a)人类β -珠蛋白和γ -珠蛋白基因在XX-8细胞中以大约相等的数量存在;(b)即使使用几种不同的诱导剂,在细胞质或核RNA中也无法检测到人γ -珠蛋白mRNA序列;(c)诱导后,人β -珠蛋白基因从DNase I不敏感或封闭结构转化为DNase I开放结构,而人γ -珠蛋白基因保持封闭结构;(d)在完整的诱导细胞中没有检测到人β -珠蛋白多肽,这表明成纤维细胞珠蛋白基因,即使在红系环境中诱导产生mRNA,也不能合成有效翻译的RNA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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