Nucleotide sugar transporters: Biological and functional aspects

被引:77
作者
Gerardy-Schahn, R
Oelmann, S
Bakker, H
机构
[1] Hannover Med Sch, Inst Physiol Chem, D-30625 Hannover, Germany
[2] Univ Wageningen & Res Ctr, Plant Res Int, NL-6700 AA Wageningen, Netherlands
关键词
nucleotide sugar transporter; Golgi complex; type III protein; congenital disorder of glycosylation type II (CDG IIc);
D O I
10.1016/S0300-9084(01)01322-0
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
The Golgi apparatus serves as the major site of glycosylation reactions. Nucleotide sugars which are substrates of the Golgi localized glycosyltransferases are synthesized in the cytoplasm (cell nucleus in case of CMP-sialic acid) and must be transported into the compartment lumen. This transport function is carried out by nucleotide sugar transporters. The first genes were cloned in the year 1996 and revealed a family of structurally conserved multi-transmembrane-spanning proteins. Due to the high structural and functional conservation, the identification of many putative nucleotide sugar transporter sequences has become possible in the existing gene data bases and accelerates the increase in knowledge on structure-function-relationships. Recent developments in the nucleotide sugar transporter field are discussed in this article. (C) 2001 Societe francaise de biochimie et biologie moleculaire/Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:775 / 782
页数:8
相关论文
共 59 条
[1]   Molecular characterization of Vig4/Vrg4 GDP-mannose transporter of the yeast Saccharomyces cerevisiae [J].
Abe, M ;
Hashimoto, H ;
Yoda, K .
FEBS LETTERS, 1999, 458 (03) :309-312
[2]   Molecular cloning of the Golgi apparatus uridine diphosphate-N-acetylglucosamine transporter from Kluyveromyces lactis [J].
Abeijon, C ;
Robbins, PW ;
Hirschberg, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :5963-5968
[3]   Expression and activity of chimeric molecules between human UDP-galactose transporter and CMP-sialic acid transporter [J].
Aoki, K ;
Sun-Wada, GH ;
Segawa, H ;
Yoshioka, S ;
Ishida, N ;
Kawakita, M .
JOURNAL OF BIOCHEMISTRY, 1999, 126 (05) :940-950
[4]  
AOKI K, 2001, IN PRESS J BIOL CHEM
[5]   SQV-7, a protein involved in Caenorhabditis elegans epithelial invagination and early embryogenesis, transports UDP-glucuronic acid, UDP-N-acetylgalactosamine, and UDP-galactose [J].
Berninsone, P ;
Hwang, HY ;
Zemtseva, I ;
Horvitz, HR ;
Hirschberg, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (07) :3738-3743
[6]   Functional expression of the murine gels CMP-sialic acid transporter in Saccharomyces cerevisiae [J].
Berninsone, P ;
Eckhardt, M ;
GerardySchahn, R ;
Hirschberg, CB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (19) :12616-12619
[7]   Nucleotide sugar transporters of the Golgi apparatus [J].
Berninsone, PM ;
Hirschberg, CB .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2000, 10 (05) :542-547
[8]   sqv-3 -7, and -8, a set of genes affecting morphogenesis in Caenorhabditis elegans, encode enzymes required for glycosaminoglycan biosynthesis [J].
Bulik, DA ;
Wei, G ;
Toyoda, H ;
Kinoshita-Toyoda, A ;
Waldrip, WR ;
Esko, JD ;
Robbins, PW ;
Selleck, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (20) :10838-10843
[9]   Membrane topology of the mammalian CMP-sialic acid transporter [J].
Eckhardt, M ;
Gotza, B ;
Gerardy-Schahn, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :8779-8787
[10]   Mutants of the CMP-sialic acid transporter causing the Lec2 phenotype [J].
Eckhardt, M ;
Gotza, B ;
Gerardy-Schahn, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (32) :20189-20195