首页> 美国卫生研究院文献>Journal of Virology >The amphotropic murine leukemia virus receptor gene encodes a 71-kilodalton protein that is induced by phosphate depletion.
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The amphotropic murine leukemia virus receptor gene encodes a 71-kilodalton protein that is induced by phosphate depletion.

机译:两性鼠类白血病病毒受体基因编码由磷酸盐耗竭诱导的71千达尔顿蛋白。

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摘要

The amphotropic murine leukemia virus (MuLV) can infect cells from a number of mammals, including humans, via its specific receptor. Basic knowledge of amphotropic MuLV receptor expression is likely to be useful in the development and improvement of gene therapy protocols based on amphotropic-pseudotyped vectors. To investigate the expression of the human receptor for the amphotropic MuLV (GLVR-2, newly termed Pit2), we determined its mRNA levels in several cell lines and found them to vary significantly. Induction of increased levels of mRNA after removal of phosphate from the media was observed in two osteosarcoma cell lines. The increase in GLVR-2 mRNA resulted in a concomitant rise in the levels of a 71-kDa protein specifically recognized by affinity-purified antibodies against GLVR-2. Using these antibodies, we were able to confirm the intracellular topology of the large hydrophilic domain between the proposed sixth and seventh transmembrane domains of the GLVR-2 protein. This assignment is in agreement with the fourth extracellular loop being outside the cell, consistent with the proposal that the fourth extracellular loop of GLVR-2 contains the envelope binding site.
机译:两性鼠类白血病病毒(MuLV)可以通过其特异性受体感染包括人类在内的许多哺乳动物的细胞。两性MuLV受体表达的基础知识可能在基于两性假型载体的基因治疗方案的开发和改进中有用。为了研究两性MuLV(GLVR-2,新称为Pit2)的人类受体的表达,我们确定了其在几种细胞系中的mRNA水平,并发现它们之间存在显着差异。在两种骨肉瘤细胞系中观察到从培养基中去除磷酸盐后诱导增加的mRNA水平。 GLVR-2 mRNA的增加导致被亲和纯化的GLVR-2抗体特异性识别的71-kDa蛋白水平随之升高。使用这些抗体,我们能够确认GLVR-2蛋白第六和第七跨膜结构域之间的大亲水域的细胞内拓扑。该分配与细胞外的第四细胞外环一致,这与GLVR-2的第四细胞外环包含包膜结合位点的提议一致。

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