Characterization of seven low incidence blood group antigens carried by erythrocyte band 3 protein

被引:29
作者
Jarolim, P
Rubin, HL
Zakova, D
Storry, J
Reid, ME
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Pathol, Boston, MA 02111 USA
[2] Inst Hematol & Blood Transfus, CR-12820 Prague, Czech Republic
[3] Tufts Univ, Sch Med, St Elizabeths Med Ctr, Dept Biomed Res, Boston, MA 02111 USA
[4] New York Blood Ctr, Imunohematol Lab, New York, NY 10021 USA
关键词
D O I
10.1182/blood.V92.12.4836.424k24_4836_4843
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent studies have demonstrated that band 3 carries antigens of the Diego blood group system and have elucidated the molecular basis of several previously unassigned low incidence and high incidence antigens. Because the available serological data suggested that band 3 may carry additional low incidence blood group antigens, we screened band 3 genomic DNA encoding the membrane domain of band 3 for single-strand conformational polymorphisms. We found that the putative first ectoplasmic loop of band 3 carries blood group antigen ELO, 432 Arg-->Trp; the third putative loop harbors antigens Vg(a) (Van Vugt), 555 Tyr-->His, BOW 561 Pro-->Ser, Wu (Wulfsberg), 565 Gly-->Ala, and Bp(a) (Bishop), 569 Asn-->Lys; and the putative fourth ectoplasmic loop carries antigens Hg-a (Hughes), 656 Arg-->Cys, and Mo-a (Moen), 656 Arg-->His. We studied erythrocytes from carriers of five of these blood group antigens. We found similar levels of reticulocyte mRNA corresponding to the two band 3 gene alleles, normal content and glycosylation of band 3 in the red blood cell membrane, and normal band 3-mediated sulfate influx into red blood cells, suggesting that the mutations do not have major effect on band 3 structure and function. In addition to elucidating the molecular basis of seven low incidence blood group antigens, these results help to create a more accurate structural model of band 3. (C) 1998 by The American Society of Hematology.
引用
收藏
页码:4836 / 4843
页数:8
相关论文
共 72 条
[1]  
ALPER SL, 1988, J BIOL CHEM, V263, P17092
[2]   CONFIRMATION OF ANTI-ELO AS A CAUSE OF HEMOLYTIC-DISEASE OF THE NEWBORN [J].
BETTER, PJ ;
FORD, DS ;
FRASCARELLI, A ;
STERN, DA .
VOX SANGUINIS, 1993, 65 (01) :70-70
[3]  
Bruce L. J., 1995, Transfusion (Bethesda), V35, p52S
[4]   BAND-3-HT, A HUMAN RED-CELL VARIANT ASSOCIATED WITH ACANTHOCYTOSIS AND INCREASED ANION TRANSPORT, CARRIES THE MUTATION PRO-868 -] LEU IN THE MEMBRANE DOMAIN OF BAND-3 [J].
BRUCE, LJ ;
KAY, MMB ;
LAWRENCE, C ;
TANNER, MJA .
BIOCHEMICAL JOURNAL, 1993, 293 :317-320
[5]  
BRUCE LJ, 1994, J BIOL CHEM, V269, P16155
[6]  
BRUCE LJ, 1995, BLOOD, V85, P541
[7]   Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (band 3, AE1) gene [J].
Bruce, LJ ;
Cope, DL ;
Jones, GK ;
Schofield, AE ;
Burley, M ;
Povey, S ;
Unwin, RJ ;
Wrong, O ;
Tanner, MJA .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (07) :1693-1707
[8]   The low-incidence blood group antigen, Wd(a), is associated with the substitution Val(557)->Met in human erythrocyte band 3 (AE1) [J].
Bruce, LJ ;
Zelinski, T ;
Ridgwell, K ;
Tanner, MJA .
VOX SANGUINIS, 1996, 71 (02) :118-120
[9]   A NEW LOW-FREQUENCY ANTIGEN BOW (BOWYER) [J].
CHAVES, MA ;
LEAK, MR ;
POOLE, J ;
GILES, CM .
VOX SANGUINIS, 1988, 55 (04) :241-243
[10]   CDNA CLONING AND LOCALIZATION OF A BAND 3-RELATED PROTEIN FROM ILEUM [J].
CHOW, A ;
DOBBINS, JW ;
ARONSON, PS ;
IGARASHI, P .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (03) :G345-G352