The DAU allele cluster of the RHD gene

被引:85
作者
Wagner, FF
Ladewig, B
Angert, KS
Heymann, GA
Eicher, NI
Flegel, WA
机构
[1] Univ Ulm Klinikum, Abt Transfus Med, D-89081 Ulm, Germany
[2] Inst Ulm, DRK Blutspendedienst Baden Wurttemberg Hessen, Ulm, Germany
[3] Biotest AG, Dreieich, Germany
[4] Univ Aachen Klinikum, Abt Transfus Med, Aachen, Germany
[5] Charite, Inst Transfus Med, Berlin, Germany
[6] Blutspendedienst SRK Bern, Bern, Switzerland
关键词
D O I
10.1182/blood-2002-01-0320
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Variant D occurs frequently in Africans. However, considerably less RHD alleles have been described in this population compared with Europeans. We characterized 5 new RHD alleles, dubbed DAU-0 to DAU-4, that shared a T379M substitution and occurred in a cDe haplotype. DAU-1 to DAU-4 were detected in Africans with partial D phenotypes. They harbored one and 2 additional missense mutations, respectively, dispersed throughout the RhD protein. An anti-D immunization was found in DAU-3. DAU-0 carrying T379M only was detected by screening European blood donors and expressed a normal D phenotype. Within the phylogeny of the RHD alleles, DAU formed an independent allele cluster, separate from the DIVa, weak ID type 4, and Eurasian D clusters. The characterization of the RH phylogeny provided a framework for future studies on RH alleles. The identification of the DAU alleles increased the number of known partial D alleles in Africans considerably. DAU alleles may be a major cause of antigen D variability and anti-D immunization in patients of African descent.
引用
收藏
页码:306 / 311
页数:6
相关论文
共 43 条
[1]  
[Anonymous], TRANSFUS MED S
[2]   The Rh blood group system: a review [J].
Avent, ND ;
Reid, ME .
BLOOD, 2000, 95 (02) :375-387
[3]   Molecular analysis of Rh transcripts and polypeptides from individuals expressing the D-VI variant phenotype: An RHD gene deletion event does not generate all D(VI)ccEe phenotypes [J].
Avent, ND ;
Liu, W ;
Jones, JW ;
Scott, ML ;
Voak, D ;
Pisacka, M ;
Watt, J ;
Fletcher, A .
BLOOD, 1997, 89 (05) :1779-1786
[4]   The management of hemolytic disease in the fetus and newborn [J].
Bowman, J .
SEMINARS IN PERINATOLOGY, 1997, 21 (01) :39-44
[5]   Evolution of the human RH (rhesus) blood group genes: A 50 year old prediction (partially) fulfilled [J].
Carritt, B ;
Kemp, TJ ;
Poulter, M .
HUMAN MOLECULAR GENETICS, 1997, 6 (06) :843-850
[6]  
COLIN Y, 1991, BLOOD, V78, P2747
[7]   The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis [J].
Daniels, GL ;
Faas, BHW ;
Green, CA ;
Smart, E ;
Maaskant-van Wijk, PA ;
Avent, ND ;
Zondervan, HA ;
von dem Borne, AEGK ;
van der Schoot, CE .
TRANSFUSION, 1998, 38 (10) :951-958
[8]  
DUTOIT ED, 1989, S AFR MED J, V75, P452
[9]   Involvement of Ser103 of the Rh polypeptides in G epitope formation [J].
Faas, BHW ;
Beckers, EAM ;
Simsek, S ;
Overbeeke, MAM ;
Pepper, R ;
vanRhenen, DJ ;
vondemBorne, AEGK ;
vanderSchoot, CE .
TRANSFUSION, 1996, 36 (06) :506-511
[10]   Molecular background of VS and weak C expression in blacks [J].
Faas, BHW ;
Beckers, EAM ;
Wildoer, P ;
Ligthart, PC ;
Overbeeke, MAM ;
Zondervan, HA ;
vondemBorne, AEGK ;
vanderSchoot, CE .
TRANSFUSION, 1997, 37 (01) :38-44