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人溶酶体α-甘露糖苷酶活性在转染的鼠细胞和人α-甘露糖苷酶缺陷型成纤维细胞中的表达。

Expression of human lysosomal alpha-mannosidase activity in transfected murine cells and human alpha-mannosidase deficient fibroblasts.

作者信息

Wang W, Nebes V L, Schmidt M C, Barranger J A

机构信息

Department of Human Genetics, University of Pittsburgh, Pennsylvania 15261, USA.

出版信息

Biochem Biophys Res Commun. 1996 Jul 25;224(3):619-24. doi: 10.1006/bbrc.1996.1075.

Abstract

We studied the human lysosomal alpha-mannosidase (MANB) by expressing the putative cDNA in mammalian cells, using the eucaryotic expression vector pCDE. The construct pCDE-MANB and pSV2-Neo were cotransfected into human alpha-mannosidase deficient fibroblasts and into a murine cell line and selected by culture in the presence of G418. Six G418 resistant 3T3 clones had increased alpha-mannosidase activity 2 to 3 times above the controls. Two clones from transfected human fibroblasts showed a 2 fold increase in enzyme activity. The human MANB cDNA gene was demonstrated in the target cells by Southern blot analysis and the expression of the gene was shown by RT-PCR analysis. This study is the first to successfully express the MANB gene in a human and a murine cell line. The results confirm that the putative MANB cDNA encodes the full length of lysosomal alpha-mannosidase. Molecular characterization of mannosidosis and approaches to gene therapy are now possible using this cDNA.

摘要

我们通过使用真核表达载体pCDE在哺乳动物细胞中表达推定的cDNA来研究人溶酶体α-甘露糖苷酶(MANB)。将构建体pCDE-MANB和pSV2-Neo共转染到人α-甘露糖苷酶缺陷型成纤维细胞和鼠细胞系中,并在G418存在下进行培养筛选。六个对G418有抗性的3T3克隆的α-甘露糖苷酶活性比对照增加了2至3倍。来自转染的人成纤维细胞的两个克隆的酶活性增加了2倍。通过Southern印迹分析在靶细胞中证实了人MANB cDNA基因,并通过RT-PCR分析显示了该基因的表达。本研究首次成功地在人细胞系和鼠细胞系中表达了MANB基因。结果证实推定的MANB cDNA编码溶酶体α-甘露糖苷酶的全长。利用该cDNA现在可以对甘露糖苷贮积症进行分子表征并开展基因治疗方法的研究。

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