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Molecular cloning of murine folylpoly-y-glutamate synthetase

机译:小鼠叶酰聚γ-谷氨酸合成酶的分子克隆

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摘要

Folylpoly-γ-glutamate synthetase (FPGS) is essential for mammalian cell survival and is a major determinant of eytoto.xieity and selectivity for folate antimctabolites. Here we describe the cloning of a cDNA encoding murine FPGS isolated from LI2H) leukemia cells. The amino acid sequence of murine FPGS is H2% identical to human FPCiS [1] with identical discrete regions of up to 41 residues. Murine FPGS contains two AUG initiation codons, shown to be responsible for miiochondrial and cytosolic forms of the enzyme in human cells [2]. Previous studies indicated species, tissue, and tumor specific differences in mammalian FPGS. The availability of murine FPGS expands the knowledge and understanding of the spectrum of these variations.
机译:叶酸-γ-谷氨酸合成酶(FPGS)对于哺乳动物细胞的存活至关重要,是叶酸抗代谢物的细胞毒性和选择性的主要决定因素。在这里,我们描述了从LI2H)白血病细胞分离的编码鼠FPGS的cDNA的克隆。鼠FPGS的氨基酸序列与人FPCiS [1] H2%相同,具有多达41个残基的相同离散区域。鼠FPGS包含两个AUG起始密码子,显示它们与人细胞中酶的线粒体形式和胞质形式有关[2]。先前的研究表明哺乳动物FPGS中的物种,组织和肿瘤特异性差异。鼠类FPGS的可用性扩展了对这些变异范围的了解和了解。

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