Molecular cloning and genomic analysis of mouse Gal beta 1,3GalNAc-specific GalNAc alpha 2,6-sialyltransferase

被引:57
作者
Kurosawa, N [1 ]
Inoue, M [1 ]
Yoshida, Y [1 ]
Tsuji, S [1 ]
机构
[1] RIKEN,INST PHYS & CHEM RES,FRONTIER RES PROGRAM,DEPT MOL GLYCOBIOL,WAKO,SAITAMA 35101,JAPAN
关键词
D O I
10.1074/jbc.271.25.15109
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
cDNA and genomic clones encoding mouse Gal beta 1, 3GalNAc-specific GalNAc alpha 2,6-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 STG6alNA I (GalNAc alpha 2,6-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 Gal beta 1,3GalNAc-specific GalNAc alpha 2,6-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.
引用
收藏
页码:15109 / 15116
页数:8
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