Kumar R, Yang J, Eddy R L, Byers M G, Shows T B, Stanley P
Department of Cell Biology, Albert Einstein College of Medicine, New York, NY 10461.
Glycobiology. 1992 Aug;2(4):383-93. doi: 10.1093/glycob/2.4.383.
A mouse cDNA clone previously isolated from an F9 teratocarcinoma cell library and shown to confer N-acetylglucosaminyltransferase I (GlcNAc-TI) activity on Lec1 Chinese hamster ovary (CHO) cell transfectants [Kumar, R., Yang,J., Larsen,R.D. and Stanley,P. (1990) Proc. Natl. Acad Sci. USA, 87, 9948-9952] has been sequenced. The nucleotide and deduced amino acid sequences are highly homologous to previously described human and rabbit GlcNAc-TI cDNAs. A 1250 bp portion of the mouse cDNA encoding all but the first 34 amino acids of the deduced protein sequence was inducibly expressed in Escherichia coli and gave rise to a prominent fusion protein of mol. wt approximately 45 kDa whose presence correlated with high levels of GlcNAc-TI activity in cell lysates. Probes generated from the cDNA were used to show that the GlcNAc-TI gene is present in a single copy in mammals and that a homologous gene was not detectable (under low-stringency hybridization conditions) in DNA from yeast, sea urchin, Drosophila or Chaenorhaditis elegans. Genomic DNA clones that hybridized to probes generated from the GlcNAc-TI cDNA were isolated from a mouse liver library. Restriction analyses, Southern hybridization and DNA sequence analyses of subcloned genomic DNA fragments and a polymerase chain reaction (PCR) product provided evidence that the coding and 3' untranslated regions of the cDNA reside in a single exon. However, the mouse GlcNAc-TI gene (Mgat-1) includes at least one additional exon 5' of the coding region. Southern analyses of DNA from mouse-human somatic cell hybrids and in situ hybridization were used to locate the human GlcNAc-TI gene (MGAT-1) between positions q31.2 and q31.3 on chromosome 5, a region of chromosome 5 that is syntenic with a region of mouse chromosome 11. Northern analyses of adult mouse tissues revealed two GlcNAc-TI gene transcripts that are differentially expressed in different tissues.
先前从F9畸胎瘤细胞文库中分离出的一个小鼠cDNA克隆,已证实其能赋予Lec1中国仓鼠卵巢(CHO)细胞转染体N-乙酰葡糖胺基转移酶I(GlcNAc-TI)活性[库马尔,R.,杨,J.,拉森,R.D.和斯坦利,P.(1990年)《美国国家科学院院刊》,87,9948 - 9952],现已完成测序。其核苷酸序列和推导的氨基酸序列与先前描述的人类和兔GlcNAc-TI cDNA高度同源。小鼠cDNA的1250 bp部分编码了推导蛋白序列除前34个氨基酸之外的所有氨基酸,该部分在大肠杆菌中可诱导表达,并产生了一个显著的融合蛋白,其分子量约为45 kDa,该融合蛋白的存在与细胞裂解物中高水平的GlcNAc-TI活性相关。由该cDNA产生的探针用于表明GlcNAc-TI基因在哺乳动物中以单拷贝形式存在,并且在酵母、海胆、果蝇或秀丽隐杆线虫的DNA中未检测到同源基因(在低严格度杂交条件下)。与从GlcNAc-TI cDNA产生的探针杂交的基因组DNA克隆从小鼠肝脏文库中分离出来。对亚克隆的基因组DNA片段和聚合酶链反应(PCR)产物进行的限制性分析、Southern杂交和DNA序列分析提供了证据,表明cDNA的编码区和3'非翻译区位于单个外显子中。然而,小鼠GlcNAc-TI基因(Mgat-1)在编码区的5'端至少还包括一个额外的外显子。对小鼠 - 人类体细胞杂种的DNA进行Southern分析以及原位杂交,用于将人类GlcNAc-TI基因(MGAT-1)定位在5号染色体q31.2和q31.3之间的位置,5号染色体的该区域与小鼠11号染色体的一个区域是同线的。对成年小鼠组织进行的Northern分析揭示了两种GlcNAc-TI基因转录本,它们在不同组织中差异表达。