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编码鸡UDP-N-乙酰-D-葡萄糖胺(GlcNAc):GlcNAcβ1-6(GlcNAcβ1-2)-甘露糖α1-R[GlcNAc到甘露糖]β1,4-N-乙酰葡糖胺基转移酶VI的cDNA的分子克隆与表达

Molecular cloning and expression of cDNA encoding chicken UDP-N-acetyl-D-glucosamine (GlcNAc): GlcNAcbeta 1-6(GlcNAcbeta 1-2)- manalpha 1-R[GlcNAc to man]beta 1,4N-acetylglucosaminyltransferase VI.

作者信息

Sakamoto Y, Taguchi T, Honke K, Korekane H, Watanabe H, Tano Y, Dohmae N, Takio K, Horii A, Taniguchi N

机构信息

Departments of Biochemistry and Ophthalmology, Osaka University Medical School, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

J Biol Chem. 2000 Nov 17;275(46):36029-34. doi: 10.1074/jbc.M005860200.

Abstract

A cDNA that encodes UDP-N-acetyl-d-glucosamine (GlcNAc):GlcNAcbeta1-6(GlcNAcbeta1-2)Manalpha1-R[GlcNA c to Man]beta1, 4N-acetylglucosaminyltransferase VI (GnT VI), which is responsible for the formation of pentaantennary asparagine-linked oligosaccharides (N-glycans), has been cloned from a hen oviduct cDNA library based on the partial amino acid sequences of the purified enzyme. The isolated cDNA clone contained an open reading frame encoding 464 amino acids, including all of the peptides that were sequenced. The deduced amino acid sequence predicts a type II transmembrane topology and contains two potential N-glycosylation sites. The primary structure was found to be significantly similar to human GnT IV-homologue, the gene for which was cloned from the deleted region in pancreatic cancer, and to human and bovine GnT IVs. Chicken GnT VI-transfected COS-1 cells showed a high GnT VI activity (26.8 pmol/h/mg protein), whereas nontransfected, mock-transfected, or human GnT IV-homologue-transfected COS-1 cells had no activity. Northern blot analysis using poly(A)(+) RNA from hen oviduct indicated that the size of GnT VI mRNA is 2.1 kilobases. Reverse transcription-polymerase chain reaction analysis showed that GnT VI mRNA was relatively highly expressed in oviduct, spleen, lung, and colon.

摘要

一个编码UDP-N-乙酰基-D-葡糖胺(GlcNAc):GlcNAcβ1-6(GlcNAcβ1-2)Manα1-R[GlcNAc到Man]β1,4-N-乙酰葡糖胺基转移酶VI(GnT VI)的cDNA已从母鸡输卵管cDNA文库中克隆出来,该酶负责五天线型天冬酰胺连接寡糖(N-聚糖)的形成,克隆依据的是纯化酶的部分氨基酸序列。分离得到的cDNA克隆包含一个编码464个氨基酸的开放阅读框,其中包括所有已测序的肽段。推导的氨基酸序列预测其具有II型跨膜拓扑结构,并含有两个潜在的N-糖基化位点。发现其一级结构与人GnT IV同源物(该基因是从胰腺癌缺失区域克隆得到的)以及人和牛的GnT IVs具有显著相似性。用鸡GnT VI转染的COS-1细胞显示出高GnT VI活性(26.8 pmol/h/mg蛋白),而未转染、空转染或用人GnT IV同源物转染的COS-1细胞则没有活性。使用来自母鸡输卵管的聚腺苷酸(A)(+)RNA进行的Northern印迹分析表明,GnT VI mRNA的大小为2.1千碱基。逆转录-聚合酶链反应分析表明,GnT VI mRNA在输卵管、脾脏、肺和结肠中相对高表达。

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