Mitsumoto Y, Oka S, Sakuma H, Inazawa J, Kawasaki T
Department of Biological Chemistry and CREST (Core Research for Educational Science and Technology) Project, Japan Science and Technology Corporation, Kyoto, 606-8501, Japan.
Genomics. 2000 Apr 15;65(2):166-73. doi: 10.1006/geno.2000.6152.
The HNK-1 carbohydrate is expressed on various cell adhesion molecules in the nervous system and is suggested to play a role in cell-cell and cell-substrate interactions. Here we describe the isolation of a cDNA encoding human glucuronyltransferase (GlcAT-P), which is a key enzyme in the biosynthesis of the HNK-1 carbohydrate. The primary structure deduced from the cDNA sequence predicted a type II transmembrane protein of 334 amino acids. Human GlcAT-P was 98.2% identical with rat GlcAT-P in amino acid sequence, the exception being the length of the cytoplasmic tail. Northern blot analysis indicated that human GlcAT-P is expressed mainly in the brain. There is a single copy of the human GlcAT-P gene (HGMW-approved symbol B3GAT1), and it was mapped to chromosome 11q25.
HNK-1碳水化合物在神经系统的多种细胞黏附分子上表达,并被认为在细胞间和细胞与底物的相互作用中发挥作用。在此,我们描述了一种编码人葡糖醛酸基转移酶(GlcAT-P)的cDNA的分离,该酶是HNK-1碳水化合物生物合成中的关键酶。从cDNA序列推导的一级结构预测为一个334个氨基酸的II型跨膜蛋白。人GlcAT-P与大鼠GlcAT-P的氨基酸序列有98.2%的同一性,不同之处在于细胞质尾巴的长度。Northern印迹分析表明人GlcAT-P主要在脑中表达。人GlcAT-P基因有一个单拷贝(HGMW批准符号为B3GAT1),并被定位到11号染色体q25区。