DETERMINATION OF THE FREQUENCY OF THE A2M (2) ALLELE OF IMMUNOGLOBULINS-A IN TUNISIAN POPULATION USING RFLP TECHNIQUE
REVUE FRANCAISE DE TRANSFUSION ET D HEMOBIOLOGIE
Authors: FAKHFAKH, F; ROUIS, S; MAKNI, H; AYADI, H
Abstract
The human IgA2 subclass has two allotypes A2m(1) and A2m (2). Using the RFLP technique, we determined the A2m(2) frequency in a sample of 29 tunisian individuals. In accordance with Lefranc and all. [6], the presence of a polymorphic EcoRI site of the A2m(2) allele was confirmed in our RFLP study whereas no BamHI nor HindIII polymorphisms were shown. Among the 29 cases studies, 11 were heterozygous A2m2-1, 17 homozygous A2m1-1 and 1 homozygous A2m2-2. The A2m2 allele frequency in the Tunisian population (0,22) is intermediate between the Europeen frequency and the African one.
A HUMAN MYELOMA IGA WITH A HYBRID HEAVY-CHAIN RESULTING FROM PUTATIVE SOMATIC GENE CONVERSION
EUROPEAN JOURNAL OF IMMUNOLOGY
Authors: SILVAIN, C; AUCOUTURIER, P; LEDUC, I; MIHAESCO, E; PREUDHOMME, JL; COGNE, M
Abstract
A human monoclonal IgA1-IgA2lambda hybrid molecule was detected in a myeloma patient homozygous for the A2m(1) allotype during a systematic study of monoclonal IgA with subclass-specific monoclonal antibodies (mAb) and the lectin jacalin. This monoclonal immunoglobulin (GAU) reacted with both, although not with all, anti-alpha1 and anti-alpha2 mAb. Its heavy (H) chain contained an al hinge region as shown by jacalin reactivity, the presence of disulfide-linked H and light chains in spite of its belonging to the IgA2m(1) allotype and amino acid composition of the isolated hinge region. The complete sequence of the H chain was deduced from that of complementary DNA clones from bone marrow cells. The CH1 domain, hinge region and beginning of the CH2 domain and the membrane peptide were encoded by the al gene, with an insertion of an alpha2m(1) gene sequence accounting for the end of the CH2 and part or all of the CH3 domain (sequence identity between the two normal genes precludes a precise definition of breakpoints). The region of the 5' recombination site included a repeat of a six base pair sequence which might play a role in the genetic exchange. The GAU hybrid a gene was undetectable in the patient's genomic DNA from polymorphonuclear cells. The genetic event which occurred at the level of the proliferating plasma cell clone is most likely to be a gene conversion.