A molecular approach of the structure polymorphism and the consideraldy function of blood groups;Vers une approche moléculaire de la structure, du polymorphisme et de la fonction des groupes sanguins

Transfusion Clinique et Biologique

Volumn 3, Issue 3, 1996, Pages 181-210

  Cartron, J P ^a,b  

^a INSTITUT NATIONAL DE LA TRANSFUSION SANGUINE   (France)

^b Institut de Recherche en Santé   (France)

Author keywords

Blood groups; Membrane proteins; Molecular genetics; Red blood cells; Structure function

Indexed keywords

ALLOANTIGEN; BLOOD GROUP ANTIGEN; MEMBRANE PROTEIN; POLYSACCHARIDE;

BLOOD; BLOOD GROUP ABO SYSTEM; CHEMISTRY; GENETIC POLYMORPHISM; GENETICS; GENOTYPE; HUMAN; REVIEW; STRUCTURE ACTIVITY RELATION;

ABO BLOOD-GROUP SYSTEM; BLOOD GROUP ANTIGENS; GENOTYPE; HUMANS; ISOANTIGENS; MEMBRANE PROTEINS; POLYMORPHISM, GENETIC; POLYSACCHARIDES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0029688595     PISSN: 12467820     EISSN: None     Source Type: Journal    
DOI: 10.1016/s1246-7820(96)80036-x     Document Type: Article

References (71)

1. Ahearn J.M., Fearon D.T. (1989) Structure and function of the complement receptors, CR1 (CD35) and CR2 (CD21). Adv. Immunol., 46, 183-219.
2. Allosio N., Dalla Venezia N., Rana A., Andrabi K., Texier P., Gilsanz F., Cartron J.-P., Delaunay J., Chishti A.H. (1993) Evidence that the red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C. Blood, 82, 1323-1327.
3. Anstee D.J. (1995) Blood group antigens defined by the amino acid sequences of red cell surface antigens. Transfusion Med., 5, 1-13.
4. Anstee D.J. (1990) The nature and abundance of human red cell surface glycoproteins. J. Immunogenet., 17, 219-225.
5. Atkinson J.P., Lublin D.M. (1989) Decay accelerating factor : biochemistry, molecular biology and function. Ann. Rev. Immunol., 7, 35-58.
6. Aubin J.T., Le Van Kim C., Mouro I., Colin Y., Bignozzi C., Brossard Y., Cartron J.-P. Specificity and sensitivity of RHD genotyping methods by PCR-based DNA amplification. Blood, submitted for publication.
7. Bailly P., Tontti E., Hermand P., Cartron J.-P., Gahmberg C.G. (1995) The red cell LW blood group glycoproteins is an intracellular adhesion molecule (ICAM-4) which binds to CD11/CD18 leucocyte integrins. Eur. J. Immunol., 25, 3316-3320.
8. Bailly P., Hermand P., Callebaut I., Sonneborn H.H., Khamlichi S., Mornon J.P., Cartron J.-P. (1994) The LW blood group glycoprotein is homologous to intercellular adhesion molecules. Proc. Natl. Acad. Si. USA, 91, 5306-5310.
9. a antigens belong to the Dombrock blood group system. Vox Sang., 68, 177-182.
10. Bennett E.P., Steffensen R., Clausen H., Weghuis D.O., van Kessel A.G. (1995) Genomic cloning of the human histo-blood group ABO locus. Biochem. Biophys. Res. Commun., 206, 318-325.
11. Bennett P., Le Van Kim C., Colin Y., Warwick R., Cherif-Zahar B., Fisk N.M., Cartron J.-P. (1993) Prenatal determination of fetal RhD genotype by DNA amplification. N. Engl. J. Med., 329, 607-610.
12. Boren T., Falk P., Roth K.A., Larson G., Normark S. (1993) Attachment of Helicobacter pylori to human gastric epithelium mediated by blood group antigens. Science, 262, 1892-1895.
13. Brown K.E., Andeson S.M., Young N.S. (1993) Erythrocyte P antigen : cellular receptor for B19 parvovirus. Science, 262, 114-117.
14. Brown K.E., Hibbs J.R., Galliena G., Anderson S.M., Lehman E.D., McCarthy P., Young N.S. (1994) Resistance to parvovirus B19 infection due to lack of virus receptor (erythrocyte P antigen). N. Engl. J. Med., 330, 1192-1196.
15. Bruce L.J., Ring S.M., Anstee D.J., Reid M.E., Wilkinson S., Tanner M.J.A. (1995) Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3 : a site of interaction between band 3 and glycophorin A under certain conditions. Blood, 85, 541-547.
16. Cartron J.-P., Le Van Kim C., Colin Y. (1993) Glycophorin C and related glycoproteins : structure, function and regulation. Semin. Haematol., 30, 152-168.
17. Cartron J.-P., Rahuel C. (1992) Human erythrocyte glycophorins : protein and gene structure analysis. Transfusion Med. Reviews, 6, 63-92.
18. Cartron J.-P. (1994) Defining the Rh blood group antigens. Biochemistry and molecular genetics. Blood Reviews, 8, 199-212.
19. Chaudhuri A., Polykova J., Zbrzezna V., Williams K., Gulati S., Pogo A.O. (1993) Cloning of glycoprotein D cDNA, which encodes the major subunit of the Duffy blood group system and the receptor for the Plasmodium vivax malarial parasite. Proc. Natl. Acad. Si. USA, 90, 10793.
20. Chaudhuri A., Polyakova J., Zbrzezna V., Pogo O. (1995) The coding sequence of Duffy blood group gene in humans and simians : restriction fragment length polymorphism, antibody and malarial parasite specificities, and expression in nonerythroid tissues in Duffy-negative individuals. Blood, 85, 615-621.
21. Cherif-Zahar B., Raynal V., Gane P., Mattei M.G., Bailly P., Gibbs B., Colin Y., Cartron J.-P. (1996) Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency. Nature Genet, 12, 168-173.
22. Chrispeels M.J., Agre P. (1994) Aquaporins : water channel proteins of plant and animal cells. TIBS, 19, 421-425.
23. Clausen H., Bennett E.P., Grunnet N. (1994) Molecular genetics of ABO histo-blood groups. Transfus. Clin. Biol., 2, 79-89.
24. Delaunay J., Alloisio N., Morlé L., Carré G. (1995) La sphérocytose héréditaire en 1995 : l'apport de la génétique moéculaire. Hématologie, 2, 115-122.
25. Ellis N.A. Tippett P., Petty A., Reid M., Weller P.A., Ye T.Z., German J., Goodfellow P.N., Thomas S., Banting G. (1994) PBDX is the XG blood group gene. Nature Genet, 8, 285-290.
26. Feng Y., Broder C.C., Kennedy P.E., Berger E.A. (1996) HIV-1 entry cofactor : functional cDNA cloning of a seven-transmembrane G protein-coupled receptor. Science, 272, 872-876.
27. Fukuda M. (1993) Molecular genetics of the glycophorin A gene cluster. Semin. Hematol., 30, 138-151.
28. Galmiche A., Lustenberger P. (1994) CD44, invasion tumorale et métastase. Médecine/sciences, 10, 1282-1291.
29. Gelin C., Aubrit F., Phalipon A., Raynal B., Cole S., Kaczorek M., Bernard A. (1989) The E2 antigen, a 32 kd glycoprotein involved in T-cell adhesion processes, is the MIC2 gene product. EMBO J., 8, 3253-3259.
30. Haynes B.F., Telen M.J., Hale L.P., Denning S.M. (1989) CD44 - A molecule involved in leukocyte adherence and T-cell activation. Immunol. Today, 10, 423-428.
31. Ho M., Chelly J., Carter N., Danek A., Crocker P., Monaco A.P. (1994) Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein. Cell, 77, 869-880.
32. Horuk R., Chitnis C.E., Darbonne W.C., Colby T.J., Rybicki A., Hadley T.J., Miller L.H. (1993) A receptor for the malarial parasite Plasmodium vivax : the erythrocyte chemokine receptor. Science, 261, 1182-1184.
33. Iwamoto S., Li J., Omi T., Ikemoto S., Kajii E. (1996) Identification of a novel exon and spliced form of Duffy mRNA that is the predominant transcript in both erythroid and postcapillary venule endothelium. Blood, 87, 378-385.
34. Jarolim P., Murray J., Rubin H., Smart E., Zelinski T., Moulds J.M. The low incidence antigens Wda, Rba and Warr are located on band 3. 24th Congress ISBT-96, Makuhari Messe, Japan.
35. Kasinrerk W., Fiebiger E., Stefanova I., Baumruker T., Knapp W., Stockinger H. (1992) Human leucocyte activation antigen M6, a member of the Ig superfamily, is the species homologue of rat OX-47, mouse basigin, and chicken HT7 molecule. J. Immunol., 149, 847-854.
36. Khamlichi S., Bailly P., Blanchard D., Goossens D., Cartron J.-P., Bertrand O. (1995) Purification and partial characterization of the erythrocyte Kx protein deficient in Mcleod patients. Eur. J. Biochem., 228, 931-934.
37. Karlsson K.A. (1989) Animal glycosphingolipids as membrane attachment sites for bacteria. Ann. Rev. Biochem., 58, 309-350.
38. Kelly R.J., Rouquier S., Giorgi D., Lennon G.G., Lowe J.B. (1995) Sequence and expression of a candidate for the human secretor blood group a(1,2) fucosyltransferase gene (FUT2). J. Biol. Chem., 270, 4640-4649.
39. Kukowska J.F., Larsen R.D., Nair R.P., Lowe J.B. (1990) A cloned human cDNA determines espression of a mouse-stage specific embryonic antigen and the Lewis blood group a(1,3/1,4) fucosyltransferase. Genes Develop., 4, 1288-1303.
40. Larsen R.D., Ernst L.K., Nair R.P., Lowe J.B. (1990) Molecular cloning, sequence, and expression of a human GDP-L-fucose : galactoside 2-a-L-fucosyltransferase cDNA that can form the H blood group antigen. J. Biol. Chem., 87, 6674-6678.
41. Lee S., Wu X., Reid M., Zelinski T., Redman C.M. (1995) Molecular basis of the Kell (K1) phenotype. Blood, 85, 912-916.
42. Lee S., Zambas E., Green E.D., Redman C.M. (1995) Organization of the gene encoding the human Kell blood group protein. Blood, 85, 1364-1370.
43. Lowe J.B. (1991) Molecular cloning, expression and uses of mammalian glycosyltransferases. Semin. Cell. Biol., 2, 289-307.
44. Lublin D.M., Mallison G., Poole J., Reid M.E., Thompson E.S., Ferdman B.R., Telen M.J., Anstee D.J., Tanner M.J.A. (1994) Molecular basis of reduced or absent expression of decay accelerating factor in Cromer blood group phenotypes. Blood, 84, 1276-1282.
45. Mallinson G., Soo K.S., Schall T.J., Pisacka M., Anstee D.J. (1995) Mutations in the erythrocyte chemokine receptor (Duffy) gene : the molecular basis of the Fya/Fyb antigens and identification of a deletion in the Duffy gene of an apparently healthy individual with the Fy(a-b-) phenotype. Br. J. Haematol., 90, 823-829.
46. Mollicone R., Candelier J.J., Reguine I., Couillin P., Fletcher A., Oriol R. (1994) Molecular genetics of α-L-fucosyltransferase genes (H, Se, Le, FUT4, FUT5 and FUT6). Transfus. Clin. Biol., 2, 91-97.
47. Morinet F., Tchernia G. (1991) Le parvovirus B19 et l'hématopoïèse. Medecine/sciences, 7, 127-137.
48. Moulds J.M., Nickells N.W., Moulds J.J., Brown M.C., Atkinson J.P. (1991) The C3b/C4b receptor is recognized by the Knops, McCoy, Swain-Langley, and York blood group antisera. J. Exp. Med., 173, 1159-1163.
49. Moulds J.M., Nowicki S., Moulds J.J., Nowicki B.J. (1996) Human blood groups : incidental receptors for viruses and bacteria. Transfusion, 36, 362-374.
50. Mouro I., Colin Y., Cherif-Zahar B., Cartron J.-P. Le Van Kim C. (1993) Molecular genetic basis of the human RH blood group system. Nature Genet., 5, 62-65.
51. Neote K., Mak J.Y., Kolakovski L.F., Schall T.J. (1994) Functional and biochemical analysis of the cloned Duffy antigen : identity with the red blood cell chemokine receptor. Blood, 84 44-52.
52. Olivès B., Mattei M.G., Huet M., Neau P., Martial S., Cartron J.-P., Bailly P. (1995) Kidd blood group and urea transport function of human erythrocytes are carried by the same protein. J. Biol. Chem., 270, 15607-15610.
53. Parsons S.F., Jones J., Anstee D.J., Judson P.A., Gardner B., Wiener E., Poole J., Illum N., Wickramasinghe S.N. (1994) A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and unique blood group phenotype [In(a-b-), Co(a-b-)]. Blood, 83, 860-868.
54. Parsons S.F., Mallinson G., Holmes C.H., Houlihan J.M., Simpson, K.L., Mawby W.J., Spurr N.K., Warne D., Barclay A.N., Anstee D.J. (1995) The Lutheran blood group glycoprotein, another member of the immunoglobulin superfamily, is widely expressed in human tissues and is developmentally regulated in human liver. Proc. Natl. Acad. Sci. USA, 92, 5496-5500.
55. a and CD99 (12E7 antigen) on red cells. Vox Sang., 69, 231-235.
56. Preston G.M., Smith B.L., Zeidel M.L., Moulds J.J., Agre P. (1994) Mutations in phenotypically normal humans without functional CHIP water channels. Science, 265, 1585-1587.
57. Rahuel C., Le Van Kim C., Mattei M.G., Cartron J.-P., Colin Y. A unique gene encodes spliceoforms of the B-CAM cell surface glycoprotein of epithelial cancer and of the Lutheran blood group glycoprotein. Blood, in press.
58. Rao N., Ferguson D.J., Lee S.F., Telen M.J. (1991) Identification of human erythrocyte blood group antigens on the C3b/C4b receptor. J. Immunol., 146, 3502-3507.
59. Redman C.M., Marsh W.L. (1993) The Kell blood group system and the McLeod phenotype. Semin. Hematol., 30, 209-218.
60. Rosse W.F., Ware R.E. (1995) The molecular basis of paroxysmal nocturnal hemoglobinuria. Blood, 86, 3277-3286.
61. Rouillac C., Colin Y., Hughes-Jones N.C., Beolet M., D'Ambrosio A-M., Cartron J.-P., Le Van Kim C. (1995) Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes. Blood, 85, 2937-2944.
62. Ruff P., Speicher D.W., Husain-Chishti A.H. (1991) Molecular identification of a major palmitoylated erythrocyte membrane protein containing the src homology 3 motif. Proc. Natl. Acad. Sci. USA, 88, 6595-6599.
63. Spring F.A. (1993) Characterization of blood group active erythrocyte membrane proteins with human sera. Transfusion Med., 3, 167-178.
64. Tanner M.J.A. (1993) Molecular and cellular biology of the erythrocyte anion exchanger (AE1). Semin. Hematol., 30, 34-57.
65. Telen M.J. (1995) Blood group antigens on complement receptor/regulatory proteins. Transfusion Med. Reviews, 9, 20-28.
66. Telen M.J. (1995) Erythrocyte blood group antigens : not so simple after all. Blood, 85, 299-306.
67. a epitopes of decay accelerating factor : toward the use of recombinant antigens in immunohematology. Blood, 84, 3205-3211.
68. Tournamille C., Colin Y., Cartron J.-P., Le Van Kim C. (1995) Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals. Nature Genet., 10, 224-228.
69. b blood group polymorphism. Human Genet., 95, 407-410.
70. Yamamoto F., Clausen H., White T., Marken J., Hakomori S.I. (1990) Molecular genetic basis of the histo-blood group ABO system. Nature, 345, 229-233.
71. Yamamoto F. (1995) Molecular genetics of the ABO histo-blood group system. Vox Sang., 69, 1-7.