The first constant-domain (CH1) exon of human IGHG2 is polymorphic and in strong linkage disequilibrium with the CH2 exon polymorphism encoding the G2m(n+) allotype in Caucasians

Here we describe a hitherto unknown proline/threonine polymorphism at resid ue 72 of the human IgG2 CH1 domain (EU numbering 189) and show that it is l inked to the known valine/methionine polymorphism at residue 52 of CH2 (EU numbering 282) defining the G2m(n+)/G2m(n-) allotypes. We sequenced the ent ire constant region of the heavy-chain gene for secreted IgG2 in five IGHG2 *02 homozygous individuals covering CH1, hinge, CH2, and CH3 regions (appro ximate to2 kb). Proline 72 in CHI of G2m(n-) is changed to threonine in the G2m(n+) [G2m(23)] allotype. Based on the crystal structure of human IgG1, this amino acid position is expected to be surface exposed in IgG2. Besides this structural difference, we identified two silent nucleotide polymorphi sms in the CH1 region and seven in the introns. Finally, we developed a seq uence-specific PCR typing system detecting the polymorphisms in the CH1 and CH2 regions. We typed 64 Danish Caucasians and found that the CH1 and CH2 region polymorphisms are in complete linkage disequilibrium in this populat ion.