Table I.

Distribution of VH gene somatic mutation in IL-21−/− and IL-21R−/− memory B cells

Genotype VH186.2 VH186.2+a Unmutated Position 33 mutationb VH mutation frequency Excluding germline sequences 
      Position 33 W→Lb VH mutation frequency 
   % (number% (number %  
C57BL/6 24 8 (2) 54 (13) 5.1 ± 3.1 59 5.55 ± 2.8 
IL-21−/− 12 42 (5) 8 (1)# 1.7 ± 2.5** 14# 2.86 ± 2.8# 
IL-21R−/− 28 61 (17) 7 (2)* 1.0 ± 1.9** 18# 2.64 ± 2.2** 
Genotype VH186.2 VH186.2+a Unmutated Position 33 mutationb VH mutation frequency Excluding germline sequences 
      Position 33 W→Lb VH mutation frequency 
   % (number% (number %  
C57BL/6 24 8 (2) 54 (13) 5.1 ± 3.1 59 5.55 ± 2.8 
IL-21−/− 12 42 (5) 8 (1)# 1.7 ± 2.5** 14# 2.86 ± 2.8# 
IL-21R−/− 28 61 (17) 7 (2)* 1.0 ± 1.9** 18# 2.64 ± 2.2** 

The VH mutation frequency is shown as mean mutation per VH gene. The VH mutation frequency ranges are the following: C57BL/6, 0–8; IL-21−/−, 0–9; IL-21R−/−, 0–7.

#, P < 0.05; *, P < 0.005; **, P < 0.001.

a

Sequences from single cell PCR were analyzed exactly as previously described (Blink et al., 2005) to define VH186.2 and mutations.

b

Percentage of sequences containing mutations that results in an amino acid replacement of tryptophan with leucine at position 33.

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