An allotype-associated polymorphism in the gamma3 promoter determines the germ-line gamma3 transcriptional rate but does not influence switching and subsequent IgG3 production

Eur J Immunol. 2000 Aug;30(8):2388-93. doi: 10.1002/1521-4141(2000)30:8<2388::AID-IMMU2388>3.0.CO;2-C.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes / metabolism
  • Cell Line
  • Humans
  • Immunoglobulin Allotypes / genetics*
  • Immunoglobulin Class Switching*
  • Immunoglobulin G / biosynthesis
  • Immunoglobulin G / classification
  • Immunoglobulin G / genetics*
  • Polymorphism, Genetic*
  • Promoter Regions, Genetic*
  • Transcription, Genetic*

Substances

  • Immunoglobulin Allotypes
  • Immunoglobulin G