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小鼠中两个硫酸乙酰肝素氨基葡萄糖N-脱乙酰酶/N-磺基转移酶基因的鉴定与表达

Identification and expression in mouse of two heparan sulfate glucosaminyl N-deacetylase/N-sulfotransferase genes.

作者信息

Kusche-Gullberg M, Eriksson I, Pikas D S, Kjellén L

机构信息

Department of Medical Biochemistry and Microbiology, University of Uppsala, S 751 23 Uppsala, Sweden.

出版信息

J Biol Chem. 1998 May 8;273(19):11902-7. doi: 10.1074/jbc.273.19.11902.

Abstract

The biosynthesis of heparan sulfate/heparin is a complex process that requires the coordinate action of a number of different enzymes. In close connection with polymerization of the polysaccharide chain, the modification reactions are initiated by N-deacetylation followed by N-sulfation of N-acetylglucosamine units. These two reactions are carried out by a single protein. Proteins with such dual activities were first purified and cloned from rat liver and mouse mastocytoma. The mouse mastocytoma enzyme is encoded by an approximately 4-kilobase (kb) mRNA, whereas the rat liver transcript contains approximately 8 kb. In the present study, the primary structure of the enzyme encoded by the mouse 8-kb transcript is described. It is demonstrated that both the 4-and 8-kb transcripts have a wide tissue distribution and that they are encoded by separate genes. Characterization of the gene encoding the 4-kb transcript demonstrates that it spans a region of about 8 kb and that it contains at least 14 exons. The similarity of this gene and the previously characterized human gene for the 8-kb transcript is discussed.

摘要

硫酸乙酰肝素/肝素的生物合成是一个复杂的过程,需要多种不同酶的协同作用。与多糖链的聚合密切相关,修饰反应由N - 乙酰葡糖胺单元的N - 脱乙酰化随后是N - 硫酸化引发。这两个反应由单一蛋白质进行。具有这种双重活性的蛋白质首先从大鼠肝脏和小鼠肥大细胞瘤中纯化并克隆。小鼠肥大细胞瘤酶由大约4千碱基(kb)的mRNA编码,而大鼠肝脏转录本约含8 kb。在本研究中,描述了由小鼠8 kb转录本编码的酶的一级结构。结果表明,4 kb和8 kb的转录本都具有广泛的组织分布,并且它们由不同的基因编码。对编码4 kb转录本的基因的表征表明,它跨越约8 kb的区域,并且包含至少14个外显子。讨论了该基因与先前表征的人类8 kb转录本基因的相似性。

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