Phenotype prediction by DNA-based typing of clinically significant blood group systems in Jordanian blood donors

Vox Sanguinis

Volumn 83, Issue 1, 2002, Pages 55-62

  Irshaid, N M ^a,b,c   Ramadan, S ^a   Wester, E S ^a,b   Olausson, P ^b   Hellberg, A ^b   Merza, J Y ^c   Olsson, Martin ^a,b  

^a LUND UNIVERSITY   (Sweden)

^b LUND UNIVERSITY HOSPITAL   (Sweden)

^c National Blood Centre   (Jordan)

Author keywords

Allele; Blood group; Erythrocyte; Genotype; PCR; Phenotype

Indexed keywords

RHESUS D ANTIBODY;

ALLELE; ARTICLE; BLOOD DONOR; BLOOD GROUP ABO SYSTEM; BLOOD GROUP SYSTEM; BLOOD SAMPLING; CELL ISOLATION; DNA POLYMORPHISM; DNA SEQUENCE; ERYTHROCYTE; ETHNIC GROUP; EVALUATION; EXON; GENOTYPE; HUMAN; JORDAN; PHENOTYPE; POLYMERASE CHAIN REACTION; PREDICTION; PRIORITY JOURNAL; PSEUDOGENE; SEROLOGY;

ALLELES; BLOOD DONORS; BLOOD GROUP ANTIGENS; BLOOD GROUPING AND CROSSMATCHING; DNA PRIMERS; GENE FREQUENCY; GENOTYPE; HUMANS; IMMUNOPHENOTYPING; JORDAN; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA;

EID: 0038079706     PISSN: 00429007     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1423-0410.2002.00182.x     Document Type: Article

References (30)

1. Issitt P, Anstee DJ: Applied Blood Group Serology, edn 4. Miami, FL, USA, Montgomery Scientific Publications, 1998
2. Olsson ML, Chester MA: Polymorphism and recombination events at the ABO locus: a major challenge for genomic ABO blood grouping strategies. Transfus Med 2001; 11:295-313
3. Flegel WA, Wagner FF, Muller TH, Gassner C: Rh phenotype prediction by DNA typing and its application to practice. Transfus Med 1998; 8:281-302
4. Kroll H, Carl B, Santoso S, Bux J, Bein G: Workshop report on the genotyping of blood cell alloantigens. Transfus Med 2001; 11:211-219
5. Chester MA, Olsson ML: The ABO blood group gene - a locus of considerable genetic diversity. Transfus Med Rev 2001; 15:177-200
6. Okuda H, Kawano M, Iwamoto S, Tanaka M, Seno T, Okubo Y, Kajii E: The RHD gene is highly detectable in RhD-negative Japanese donors. J Clin Invest 1997; 100:373-379
7. Singleton BK, Green CA, Avent ND, Martin PG, Smart E, Daka A, Narter-Olaga EG, Lawthorne LM, Daniels G: The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the RhD-negative blood group phenotype. Blood 2000; 95:12-18
8. 1 discriminating nucleotide substitution at the ABO locus. Vox Sang 1995; 69:242-247
9. Olsson ML, Chester MA. Polymorphisms at the ABO locus in subgroup A individuals. Transfusion 1996; 36:309-313
10. 1 gene at the blood group ABO locus. Vox Sang 1996; 70:26-30
11. Irshaid NM, Chester MA, Olsson ML: Allele-related variation in minisatellite repeats involved in the transcription of the blood group ABO gene. Transfus Med 1999; 9:219-226
12. Simsek S, Faas BH, Bleeker PM, Overbeeke MA, Cuijpers HT, van der Schoot CE, dem Borne AE: Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA. Blood 1995; 85:2975-2980
13. Gassner C, Schmarda A, Kilga-Nogler S, Jenny-Feldkircher B, Rainer E, Muller TH, Wagner FF, Flegel WA, Schonitzer D: RHD/CE typing by polymerase chain reaction using sequence-specific primers. Transfusion 1997; 37:1020-1026
14. Avent ND, Martin PG: Kell typing by allele-specific PCR (ASP). Br J Haematol 1996; 93:728-730
15. Lee S, Wu X, Reid M, Zelinski T, Redman C: Molecular basis of the Kell (K1) phenotype. Blood 1995; 85:912-916
16. Irshaid NM, Thuresson B, Olsson ML: Genomic typing of the Kidd blood group locus by a single-tube allele-specific primer PCR technique. Br J Haematol 1998; 102:1010-1014
17. Irshaid NM, Henry SM, Olsson ML: Genomic characterization of the Kidd blood group gene: different molecular basis of the Jk (a-b-) phenotype in Polynesians and Finns. Transfusion 2000; 40:69-74
18. Olsson ML, Hansson C, Avent ND, Åkesson IE, Green CA, Daniels GL: A clinically applicable method for determining the three major alleles at the Duffy (FY) blood group locus using polymerase chain reaction with allele-specific primers. Transfusion 1998; 38:168-173
19. Olsson ML, Smythe JS, Hansson C, Poole J, Mallinson G, Jones J, Avent NA, Daniels G: The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein. Br J Haematol 1998; 103:1184-1191
20. Miller SA, Dykes DD, Polesky HF: A simple salting out procedure for extracting DNA from human nucleated cells. Nucl Acids Res 1988; 16:1215
21. Olsson ML, Irshaid NM, Hosseini-Maaf B, Hellberg A, Moulds MK, Sareneva H, Chester MA: Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles. Blood 2001; 98:1585-1593
22. Bennett PR, Le Van KC, Colin Y, Warwick RM, Cherif-Zahar B, Fisk NM, Cartron JP: Prenatal determination of fetal RhD type by DNA amplification. N Engl J Med 1993; 329:607-610
23. Avent ND: Antenatal genotyping of the blood groups of the fetus. Vox Sang 1998; 74:365-374
24. Ogasawara K, Yabe R, Uchikawa M, Saitou N, Bannai M, Nakata K, Takenaka M, Fujisawa K, Ishikawa Y, Juji T, Tokunaga K: Molecular genetic analysis of variant phenotypes of the ABO blood group system. Blood 1996; 88:2732-2737
25. Kominato Y, Tsuchiya T, Hata N, Takizawa H, Yamamoto F: Transcription of human ABO histo-blood group genes is dependent upon binding of transcription factor CBF/NF-Y to minisatellite sequence. J Biol Chem 1997; 272:25890-25898
26. Parasol N, Reid M, Rios M, Castilho L, Harari I, Kosower NS: A novel mutation in the coding sequence of the FY*B allele of the Duffy chemokine receptor gene is associated with an altered erythrocyte phenotype. Blood 1998; 92:2237-2243
27. Tournamille C, Le Van KC, Gane P, Le Pennec PY, Roubinet F, Babinet J, Cartron JP, Colin Y: Arg89Cys substitution results in very low membrane expression of the Duffy antigen/receptor for chemokines in Fy(x) individuals. Blood 1998; 92:2147-2156
28. Moulds JM, Hayes S, Wells TD: DNA analysis of Duffy genes in American blacks. Vox Sang 1998; 74:248-252
29. Mallinson G, Soo KS, Schall TJ, Pisacka M, Anstee DJ: 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 1995; 90:823-829
30. Rios M, Chaudhuri A, Mallinson G, Sausais L, Gomensoro-Garcia AE, Hannon J, Rosenberger S, Poole J, Burgess G, Pogo O, Reid M: New genotypes in Fy (a-b-) individuals: nonsense mutations (Trp to stop) in the coding sequence of either FY A or FY B. Br J Haematol 2000; 108:448-454