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小鼠β1,3-半乳糖-N-乙酰半乳糖胺特异性N-乙酰半乳糖胺α2,6-唾液酸转移酶的分子克隆与基因组分析

Molecular cloning and genomic analysis of mouse Galbeta1, 3GalNAc-specific GalNAc alpha2,6-sialyltransferase.

作者信息

Kurosawa N, Inoue M, Yoshida Y, Tsuji S

机构信息

Department of Molecular Glycobiology, Frontier Research Program, Institute of Physical and Chemical Research (RIKEN), Wako, Saitama 351-01, Japan.

出版信息

J Biol Chem. 1996 Jun 21;271(25):15109-16. doi: 10.1074/jbc.271.25.15109.

Abstract

cDNA and genomic clones encoding mouse Galbeta1, 3GalNAc-specific GalNAc alpha2,6-sialyltransferase (ST6GalNAc II) were isolated, and the structure organization of the gene was determined. The predicted amino acid sequence is 57.4% identical to the chick ST6GalNAc II sequence but 33.8% identical to the chick ST6GalNA I (GalNAc alpha2, 6-sialyltransferase) sequence. The ST6GalNAc II gene is constitutively expressed in various mouse tissues but highly expressed in lactating mammary gland and adult testis. The gene contains nine exons spanning about 25 kilobases of genomic DNA and encodes a messenger RNA of 1995 nucleotides. Primer extension and S1 nuclease protection analysis of submaxillary gland mRNA showed that the transcription of the ST6GalNAc II gene starts from 68 nucleotides upstream from the translation start site. Characterization of 5'-flanking genomic regions indicated that the Galbeta1,3GalNAc-specific GalNAc alpha2,6-sialyltransferase promoter is embedded in a G+C-rich domain and contains no TATA or CAAT box but has putative binding sites for transcription factors Sp1 and AP-2. Transient transfection experiments involving luciferase reporter genes demonstrated promoter activity in NIH3T3 cells.

摘要

编码小鼠β1,3-半乳糖基-N-乙酰半乳糖胺特异性N-乙酰半乳糖胺α2,6-唾液酸转移酶(ST6GalNAc II)的cDNA和基因组克隆被分离出来,并确定了该基因的结构组织。预测的氨基酸序列与鸡的ST6GalNAc II序列有57.4%的同一性,但与鸡的ST6GalNA I(N-乙酰半乳糖胺α2,6-唾液酸转移酶)序列有33.8%的同一性。ST6GalNAc II基因在小鼠的各种组织中组成性表达,但在泌乳期乳腺和成年睾丸中高表达。该基因包含九个外显子,跨越约25千碱基的基因组DNA,并编码一个1995个核苷酸的信使RNA。对颌下腺mRNA进行引物延伸和S1核酸酶保护分析表明,ST6GalNAc II基因的转录起始于翻译起始位点上游68个核苷酸处。对5'-侧翼基因组区域的表征表明,β1,3-半乳糖基-N-乙酰半乳糖胺特异性N-乙酰半乳糖胺α2,6-唾液酸转移酶启动子嵌入在一个富含G+C的区域中,不包含TATA或CAAT框,但有转录因子Sp1和AP-2的假定结合位点。涉及荧光素酶报告基因的瞬时转染实验证明了在NIH3T3细胞中的启动子活性。

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