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嵌合人转铁蛋白基因的体外表达。

Expression of chimeric human transferrin genes in vitro.

作者信息

Fischbach K, Lu Y, Tiffany-Castiglioni E, Minter A, Bowman B H, Adrian G S

机构信息

Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio, Texas 78284.

出版信息

J Neurosci Res. 1990 Dec;27(4):633-41. doi: 10.1002/jnr.490270424.

Abstract

Transferrin (TF), a major plasma protein, binds and transports ferric iron. Evidence exists for unique roles for TF in brain in oligodendrocyte differentiation, myelination and neuronal development. In this study, 5' flanking regions of the TF gene important in regulating gene expression were identified by transfected cell studies and a comparison of 5' flanking sequences of the human TF and TF receptor genes. Human glioma cell lines HTB-16 and HTB-17 were shown to synthesize TF identical in size and immunological reaction to TF synthesized by liver. The expression of a series of human chimeric TF genes in glioma cells was compared with hepatoma and HeLa cells. A difference in transient expression was observed in hepatoma and glioma cells transfected with TF chimeric genes containing 3.9 kb of the 5' region; hepatoma cells demonstrated significantly more expression than did glioma cells, suggesting that a DNA region present in the 3.9-kb construct is important either in liver-specific expression or in repression of brain expression, or in both. Smaller constructs containing less than or equal to 0.622 kb of the 5' regulatory region of the TF gene failed to demonstrate cell-specific expression; they were expressed in HeLa cells, a line that does not synthesize TF. High levels of expression of 0.15-kb TF constructs were also observed in hepatoma and glioma cell lines, but not in transgenic mice. Possible explanations of differences observed in expression of shorter TF constructs in vitro and in vivo are discussed.

摘要

转铁蛋白(TF)是一种主要的血浆蛋白,可结合并转运三价铁。有证据表明TF在大脑中对少突胶质细胞分化、髓鞘形成和神经元发育具有独特作用。在本研究中,通过转染细胞研究以及对人TF和TF受体基因的5'侧翼序列进行比较,确定了TF基因在调节基因表达中重要的5'侧翼区域。已证明人胶质瘤细胞系HTB - 16和HTB - 17合成的TF在大小和免疫反应上与肝脏合成的TF相同。将一系列人嵌合TF基因在胶质瘤细胞中的表达与肝癌细胞和HeLa细胞进行了比较。在用含有3.9 kb 5'区域的TF嵌合基因转染的肝癌细胞和胶质瘤细胞中观察到瞬时表达存在差异;肝癌细胞的表达明显高于胶质瘤细胞,这表明3.9 - kb构建体中存在的一个DNA区域在肝脏特异性表达或大脑表达的抑制中很重要,或者在两者中都很重要。含有小于或等于0.622 kb TF基因5'调控区域的较小构建体未能表现出细胞特异性表达;它们在HeLa细胞中表达,而HeLa细胞系不合成TF。在肝癌细胞系和胶质瘤细胞系中也观察到0.15 - kb TF构建体的高水平表达,但在转基因小鼠中未观察到。讨论了在体外和体内较短TF构建体表达中观察到差异的可能解释。

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