Genomic structure of human GM3 synthase gene (hST3Gal V) and identification of mRNA isoforms in the 5′-untranslated region

被引:22
作者
Kim, KW
Kim, SW
Min, KS
Kim, CH
Lee, YC [1 ]
机构
[1] Dong A Univ, Fac Nat Resources & Life Sci, Div Biotechnol, Pusan 604714, South Korea
[2] Natl Livestock Res Inst, Div Anim Biotechnol, Suwon 441350, South Korea
[3] Dongguk Univ, Coll Oriental Med, Dept Biochem & Mol Biol, Kyung Pook 780350, South Korea
关键词
sialyltransferase; ganglioside; tissue-specific expression; fetal brain;
D O I
10.1016/S0378-1119(01)00595-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
GM3 synthase, which transfers CMP-NeuAc with an alpha2,3-linkage to a galactose residue of lactosylceramide, plays a key role in the biosynthesis of all complex gangliosides. In this study, cDNA and genomic clones encoding human GM3 synthase (hST3Gal V) were isolated, and the structural organization of the gene was determined. The hST3Gal V cDNA was identical in the coding region with cDNA that has been cloned previously from the HL-60 cells but different in the 5 ' -untranslated region (UTR). The hST3Gal V gene consisted of nine exons, which span approximately 44 kb, with exons ranging in size from 112 to 1242 bp. The coding region was located in exons 4-9, and all exon-intron boundaries except the acceptor site of intron I followed the GT-AG rule. The expression of this gene was highly restricted in both human fetal and adult tissues. By comparison of the nucleotide sequences of the genomic DNA with cDNA sequences including 5 ' -RACE products, we identified four isoforms (types 1-4) of the hST3Gal V mRNA that differ only in the 5 ' -UTR. Structural analysis of these isoforms suggests that mRNA isoforms of hST3Gal V are produced by a combination of alternative splicing and alternative promoter utilization. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:163 / 171
页数:9
相关论文
共 36 条
[1]   CELL-SPECIFIC EXPRESSION OF HUMAN BETA-GALACTOSIDE ALPHA-2,6-SIALYTRANSFERASE TRANSCRIPTS DIFFERING IN THE 5' UNTRANSLATED REGION [J].
AASHEIM, HC ;
AASENG, DA ;
DEGGERDAL, A ;
BLOMHOFF, HK ;
FUNDERUD, S ;
SMELAND, EB .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 213 (01) :467-475
[2]  
BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
[3]   3 GENES THAT ENCODE HUMAN BETA-GALACTOSIDE ALPHA-2,3-SIALYLTRANSFERASES - STRUCTURAL-ANALYSIS AND CHROMOSOMAL MAPPING STUDIES [J].
CHANG, ML ;
EDDY, RL ;
SHOWS, TB ;
LAU, JTY .
GLYCOBIOLOGY, 1995, 5 (03) :319-325
[4]   BIOSYNTHESIS AND FUNCTION OF GANGLIOSIDES [J].
FISHMAN, PH ;
BRADY, RO .
SCIENCE, 1976, 194 (4268) :906-915
[5]   Expression cloning of mouse cDNA of CMP-NeuAc:lactosylceramide α2,3-sialyltransferase, an enzyme that initiates the synthesis of gangliosides [J].
Fukumoto, S ;
Miyazaki, H ;
Goto, G ;
Urano, T ;
Furukawa, K ;
Furukawa, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (14) :9271-9276
[6]  
HAKOMORI SI, 1990, J BIOL CHEM, V265, P18713
[7]   THE C-SERIES GANGLIOSIDE-GT3, GANGLIOSIDE-GT2 AND GANGLIOSIDE-GP1C ARE FORMED IN RAT-LIVER GOLGI BY THE SAME SET OF GLYCOSYLTRANSFERASES THAT CATALYZE THE BIOSYNTHESIS OF ASIALO-SERIES, A-SERIES AND B-SERIES GANGLIOSIDES [J].
IBER, H ;
ZACHARIAS, C ;
SANDHOFF, K .
GLYCOBIOLOGY, 1992, 2 (02) :137-142
[8]   Expression cloning and functional characterization of human cDNA for ganglioside GM3 synthase [J].
Ishii, A ;
Ohta, M ;
Watanabe, Y ;
Matsuda, K ;
Ishiyama, K ;
Sakoe, K ;
Nakamura, M ;
Inokuchi, J ;
Sanai, Y ;
Saito, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :31652-31655
[9]   Combinatorial PCR approach to homology-based cloning: Cloning and expression of mouse and human GM3-synthase [J].
Kapitonov, D ;
Bieberich, E ;
Yu, RK .
GLYCOCONJUGATE JOURNAL, 1999, 16 (07) :337-350
[10]   Molecular cloning and expression of human Gal beta 1,3GalNAc alpha 2,3-sialyltransferase (hST3Gal II) [J].
Kim, YJ ;
Kim, KS ;
Kim, SH ;
Kim, CH ;
Ko, JH ;
Choe, IS ;
Tsuji, S ;
Lee, YC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 228 (02) :324-327