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人广谱特异性溶酶体酸性α-甘露糖苷酶的克隆、表达、纯化及特性分析

Cloning, expression, purification, and characterization of the human broad specificity lysosomal acid alpha-mannosidase.

作者信息

Liao Y F, Lal A, Moremen K W

机构信息

Complex Carbohydrate Research Center and the Department of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia 30602, USA.

出版信息

J Biol Chem. 1996 Nov 8;271(45):28348-58. doi: 10.1074/jbc.271.45.28348.

Abstract

We have cloned and expressed two cDNAs encoding the human lysosomal alpha-mannosidase (EC 3.2.1.24) by RT-PCR of human spleen mRNA. This enzyme is required for the degradation of N-linked carbohydrates during glycoprotein catabolism in eucaryotic cells. The shorter of the two cDNAs (3 kilobases (kb)) was found to encode an open reading frame of 2964 base pairs and, when expressed in Pichia pastoris, was found to encode an enzyme that could cleave high mannose oligosaccharides, oligosaccharides isolated from alpha-mannosidosis fibroblasts, and p-nitrophenyl-alpha-D-mannopyranoside substrates. In addition, the Pichia-expressed enzyme was inhibited by swainsonine, and had a pH optimum, Km, and Vmax characteristic of the enzyme purified previously from human liver. The second, larger RT-PCR product (3.6 kb) was found to contain an insertion and a deletion relative to the 3-kb spleen amplimer and encoded a truncated coding region, indicating that it resulted from alternate transcript splicing. No alpha-mannosidase activity could be detected in Pichia transformants containing this coding region, indicating that it did not encode a functional enzyme. Antiserum raised to the recombinant product of the 3-kb alpha-mannosidase cDNA immunoprecipitated lysosomal alpha-mannosidase activity from human fibroblast extracts. Northern blots identified a 3-kb RNA transcript in all human tissues tested, including alpha-mannosidosis fibroblasts, while minor transcripts of 3.6 kb were also present in several adult tissues. Human chromosome mapping of the mannosidase gene confirmed that the functional gene maps to the MANB locus on chromosome 19. Sequence comparisons were made to previously published human cDNA sequences encoding a putative lysosomal alpha-mannosidase (Nebes, V. L., and Schmidt, M. C. (1994) Biochem. Biophys. Res. Commun. 200, 239-245) and several differences were found relative to the functional lysosomal alpha-mannosidase encoded by the 3-kb spleen cDNA.

摘要

我们通过对人脾mRNA进行逆转录聚合酶链反应(RT-PCR),克隆并表达了两个编码人溶酶体α-甘露糖苷酶(EC 3.2.1.24)的cDNA。该酶在真核细胞糖蛋白分解代谢过程中参与N-连接碳水化合物的降解。两个cDNA中较短的一个(3千碱基(kb))编码一个2964个碱基对的开放阅读框,当在毕赤酵母中表达时,发现它编码一种能够切割高甘露糖寡糖、从α-甘露糖苷贮积症成纤维细胞中分离出的寡糖以及对硝基苯基-α-D-甘露吡喃糖苷底物的酶。此外,毕赤酵母表达的酶被苦马豆素抑制,并且具有先前从人肝脏中纯化的该酶的最佳pH值、米氏常数(Km)和最大反应速度(Vmax)特征。第二个更大的RT-PCR产物(3.6 kb)相对于3-kb的脾扩增子含有一个插入和一个缺失,并编码一个截短的编码区,表明它是由交替转录剪接产生的。在含有该编码区的毕赤酵母转化体中未检测到α-甘露糖苷酶活性,表明它不编码功能性酶。针对3-kbα-甘露糖苷酶cDNA的重组产物产生的抗血清,从人成纤维细胞提取物中免疫沉淀了溶酶体α-甘露糖苷酶活性。Northern印迹法在所有测试的人体组织中,包括α-甘露糖苷贮积症成纤维细胞中,鉴定出一个3-kb的RNA转录本,而在几个成人组织中也存在少量3.6 kb的转录本。对甘露糖苷酶基因进行人类染色体定位证实,功能性基因定位于19号染色体上的MANB位点。与先前发表的编码假定溶酶体α-甘露糖苷酶的人cDNA序列(内贝斯,V. L.,和施密特,M. C.(1994年)《生物化学与生物物理研究通讯》200,239 - 245)进行了序列比较,发现与3-kb脾cDNA编码的功能性溶酶体α-甘露糖苷酶存在一些差异。

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