GPI-anchors: An overview

被引:19
作者
Gerold, P [1 ]
Eckert, V [1 ]
Schwarz, RT [1 ]
机构
[1] UNIV MARBURG, MED CTR HYG & MED MICROBIOL, D-35037 MARBURG, GERMANY
关键词
glycoconjugate synthesis defects; glycosyl-phosphatidylinositols; glycosyltransferases; membrane proteins; pathogenicity factors;
D O I
10.4052/tigg.8.265
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
Over the last ten years since the discovery of GPI-anchoring as an alternative principle of membrane anchoring of proteins the research on these anchors has expanded dramatically. An enormous body of knowledge about their structure, biosynthesis and function has accumulated. Several systems have been studied, ranging from protozoa, yeast to mammalian cell lines, to elaborate this information. Analysis on the functional level revealed that GPIs exhibit a variety of functions beyond their mere function as membrane anchors e.g. in the maturation and transport of membrane proteins or their role in signal transduction processes and as pathogenicity factors. The recognition site for the transfer of the GPI-anchor to the native protein by the so called GPI-transamidase has been determined by the combination of biochemical and molecular genetic methods. Mutant cell lines and yeast strains with defined defects in the pathway of GPI-biosynthesis allowed the identification of the genes involved and have led to the successful cloning of several such genes. These key subjects will be dealt with in this article.
引用
收藏
页码:265 / 277
页数:13
相关论文
共 99 条
[1]  
Anderson R G, 1994, Semin Immunol, V6, P89, DOI 10.1006/smim.1994.1013
[2]   GLYCOSYLINOSITOL-PHOSPHOCERAMIDE IN THE FREE-LIVING PROTOZOAN PARAMECIUM-PRIMAURELIA - MODIFICATION OF CORE GLYCANS BY MANNOSYL PHOSPHATE [J].
AZZOUZ, N ;
STRIEPEN, B ;
GEROLD, P ;
CAPDEVILLE, Y ;
SCHWARZ, RT .
EMBO JOURNAL, 1995, 14 (18) :4422-4433
[3]   THE SACCHAROMYCES-CEREVISIAE DPM1 GENE ENCODING DOLICHOL-PHOSPHATE-MANNOSE SYNTHASE IS ABLE TO COMPLEMENT A GLYCOSYLATION-DEFECTIVE MAMMALIAN-CELL LINE [J].
BECK, PJ ;
ORLEAN, P ;
ALBRIGHT, C ;
ROBBINS, PW ;
GETHING, MJ ;
SAMBROOK, JF .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (09) :4612-4622
[4]   IDENTIFICATION OF 6 COMPLEMENTATION CLASSES INVOLVED IN THE BIOSYNTHESIS OF GLYCOSYLPHOSPHATIDYLINOSITOL ANCHORS IN SACCHAROMYCES-CEREVISIAE [J].
BENGHEZAL, M ;
LIPKE, PN ;
CONZELMANN, A .
JOURNAL OF CELL BIOLOGY, 1995, 130 (06) :1333-1344
[5]   PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH) IS CAUSED BY SOMATIC MUTATIONS IN THE PIG-A GENE [J].
BESSLER, M ;
MASON, PJ ;
HILLMEN, P ;
MIYATA, T ;
YAMADA, N ;
TAKEDA, J ;
LUZZATTO, L ;
KINOSHITA, T .
EMBO JOURNAL, 1994, 13 (01) :110-117
[6]   MECHANISM OF MEMBRANE ANCHORING AFFECTS POLARIZED EXPRESSION OF 2 PROTEINS IN MDCK CELLS [J].
BROWN, DA ;
CRISE, B ;
ROSE, JK .
SCIENCE, 1989, 245 (4925) :1499-1501
[7]   SORTING OF GPI-ANCHORED PROTEINS TO GLYCOLIPID-ENRICHED MEMBRANE SUBDOMAINS DURING TRANSPORT TO THE APICAL CELL-SURFACE [J].
BROWN, DA ;
ROSE, JK .
CELL, 1992, 68 (03) :533-544
[8]  
Capdeville Yvonne, 1993, V2 (PARTS A AND B), P181
[9]   AN INTERNALLY POSITIONED SIGNAL CAN DIRECT ATTACHMENT OF A GLYCOPHOSPHOLIPID MEMBRANE ANCHOR [J].
CARAS, IW .
JOURNAL OF CELL BIOLOGY, 1991, 113 (01) :77-85
[10]   CLONING OF DECAY-ACCELERATING FACTOR SUGGESTS NOVEL USE OF SPLICING TO GENERATE 2 PROTEINS [J].
CARAS, IW ;
DAVITZ, MA ;
RHEE, L ;
WEDDELL, G ;
MARTIN, DW ;
NUSSENZWEIG, V .
NATURE, 1987, 325 (6104) :545-549