Abstract:
:The human IgG3 (b) allotype is associated with a high and the (g) allotype with a low mean serum level of IgG3 which is due to a low frequency of B cell switching in the latter. In the present study, we found a polymorphism in position -73 (C --> A), located in the 4th NF-kappaB site of the germ-line (GL) gamma3 promoter, resulting in a significant decrease of both the basal and induced activity in the (g) allotype-associated promoter. Over-expression experiments also showed that this polymorphism reduced the synergistic activation of the promoter by Stat6 + NF-kappaB p50 / p65 or Stat6 + C / EBPgamma. A low level of GL gamma3 transcripts was also observed in individuals carrying the (g) allotype-associated promoter region. However, an individual homozygous for a crossover between the promoter and switch region, i. e. with a (g) allotype-associated promoter and a (b) allotype-associated switch region, showed a normal level of switching and IgG3 serum level. This suggests that although the (g) allotype-associated promoter is functionally inferior to that of the (b) allotype-associated promoter, these differences do not affect switching and final production of IgG3 and that polymorphisms in the switch region are more important in controlling this process.
journal_name
Eur J Immunoljournal_title
European journal of immunologyauthors
Pan Q,Petit-Frére C,Hammarström Ldoi
10.1002/1521-4141(2000)30:8<2388::AID-IMMU2388>3.0keywords:
subject
Has Abstractpub_date
2000-08-01 00:00:00pages
2388-93issue
8eissn
0014-2980issn
1521-4141pii
10.1002/1521-4141(2000)30:8<2388::AID-IMMU2388>3.0journal_volume
30pub_type
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