The blood group P1 synthase gene is identical to the Gb3/CD77 synthase gene - A clue to the solution of the P1/P2/p puzzle

被引:45
作者
Iwamura, K
Furukawa, K
Uchikawa, M
Sojka, BN
Kojima, Y
Wiels, J
Shiku, H
Urano, T
Furukawa, K
机构
[1] Nagoya Univ, Sch Med, Dept Biochem 2, Showa Ku, Nagoya, Aichi 4660065, Japan
[2] Japanese Red Cross, Tokyo Blood Ctr, Shibuya Ku, Tokyo 1500012, Japan
[3] Mie Univ, Sch Med, Dept Internal Med 2, Tsu, Mie 5148507, Japan
[4] Umea Univ Hosp, Dept Transfus Med, S-90185 Umea, Sweden
[5] Inst Gustave Roussy, CNRS, UMR 1598, F-94805 Villejuif, France
关键词
D O I
10.1074/jbc.M301609200
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
Blood group P1/P2 is a glycolipid antigen system for which the genetic mechanism has not yet been clarified. We analyzed the potential of the cloned Gb3/CD77 synthase to synthesize P1 antigen, because Gb3/CD77 and P1 share a common structure, Galalpha1,4Galbeta1,4Glc (NAc)-. L cell transfectants with Gb3/CD77 synthase cDNA expressed marginal levels of P1 on the cell surface but contained high levels of P1 in the cytoplasm. P2-type erythrocytes, which were serotyped as P2, also contained definite P1 antigen inside cells, although the amounts were lower than those of P1 cells. Only p erythrocytes lacked P1 antigen corresponding with function-losing mutations in the Gb3/CD77 synthase gene. Synthesis of P1 antigen from paragloboside in vitro was demonstrated using membrane fraction of the transfectants and a fusion enzyme with protein A. These results strongly suggested that P1 synthase is identical to Gb3/CD77 synthase and appear to propose a clue for the solution of the long-pending P1/P2/p puzzle. The P1/P2 difference might result from the difference in P1 quantity based on either different enzyme activity or the presence/absence of other enzyme modulators. Because P2 erythrocytes showed lower levels of Gb3/CD77 synthase mRNA than P1, 5'-upstream promoter regions were analyzed, resulting in the identification of two P2-specific homozygous mutations. Differences in the transcriptional regulation in erythrocytes might be a major factor determining P1/P2.
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页码:44429 / 44438
页数:10
相关论文
共 35 条
[1]   BIOSYNTHESIS OF THE BLOOD GROUP-PK AND P1 ANTIGENS BY HUMAN KIDNEY MICROSOMES [J].
BAILLY, P ;
PILLER, F ;
GILLARD, B ;
VEYRIERES, A ;
MARCUS, D ;
CARTRON, JP .
CARBOHYDRATE RESEARCH, 1992, 228 (01) :277-287
[2]   CHARACTERIZATION OF A MURINE MONOCLONAL-ANTIBODY SPECIFIC FOR THE HUMAN P1 BLOOD-GROUP ANTIGEN [J].
BAILLY, P ;
CHEVALEYRE, J ;
SONDAG, D ;
FRANCOISGERARD, C ;
PIQUET, Y ;
VEZON, G ;
CARTRON, JP .
MOLECULAR IMMUNOLOGY, 1987, 24 (02) :171-176
[3]   CRYPTIC A-LIKE RECEPTOR-SITES IN HUMAN ERYTHROCYTE GLYCOPROTEINS - PROPOSED NATURE OF TN-ANTIGEN [J].
DAHR, W ;
UHLENBRUCK, G ;
BIRD, GWG .
VOX SANGUINIS, 1974, 27 (01) :29-42
[4]   Terminology for red cell surface antigens - ISBT Working Party Oslo Report [J].
Daniels, GL ;
Anstee, DJ ;
Cartron, JP ;
Dahr, W ;
Garratty, G ;
Henry, S ;
Jorgensen, J ;
Judd, WJ ;
Kornstad, L ;
Levene, C ;
Lomas-Francis, C ;
Lubenko, A ;
Moulds, JJ ;
Moulds, JM ;
Moulds, M ;
Overbeeke, M ;
Reid, ME ;
Rouger, P ;
Scott, M ;
Seidl, S ;
Sistonen, P ;
Tani, Y ;
Wendel, S ;
Zelinski, T .
VOX SANGUINIS, 1999, 77 (01) :52-57
[5]   BLOOD-GROUP-II ACTIVE GANGLIOSIDES OF HUMAN ERYTHROCYTE-MEMBRANES [J].
FEIZI, T ;
CHILDS, RA ;
HAKOMORI, SI ;
POWELL, ME .
BIOCHEMICAL JOURNAL, 1978, 173 (01) :245-254
[6]  
FLETCHER KS, 1979, J BIOL CHEM, V254, P1196
[7]   Molecular basis for the p phenotype -: Identification of distinct and multiple mutations in the (α1,4-galactosyltransferase gene in Swedish and Japanese individuals [J].
Furukawa, K ;
Iwamura, K ;
Uchikawa, M ;
Sojka, BN ;
Wiels, J ;
Okajima, T ;
Urano, T ;
Furukawa, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37752-37756
[8]   ANALYSIS OF THE SPECIFICITY OF 5 MURINE ANTI-BLOOD GROUP-A MONOCLONAL-ANTIBODIES, INCLUDING ONE THAT IDENTIFIES TYPE-3 AND TYPE-4 A-DETERMINANTS [J].
FURUKAWA, K ;
CLAUSEN, H ;
HAKOMORI, S ;
SAKAMOTO, J ;
LOOK, K ;
LUNDBLAD, A ;
MATTES, MJ ;
LLOYD, KO .
BIOCHEMISTRY, 1985, 24 (26) :7820-7826
[9]   Expression of the Gb3/CD77 synthase gene in megakaryoblastic leukemia cells - Implication in the sensitivity to verotoxins [J].
Furukawa, K ;
Yokoyama, K ;
Sato, T ;
Wiels, J ;
Hirayama, Y ;
Ohta, M ;
Furukawa, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) :11247-11254
[10]  
Ishikawa D, 2000, METHOD ENZYMOL, V312, P157