Table 2.

Somatic mutations in S107 VH sequences cloned from class-switched B cells of VavP-Bcl2 transgenic mice


Parameter

Productive sequences

Nonproductive sequences

P (productive vs nonproductive)

P (targeted productive vs random)*
Mutations   94   63   .93   
Ratio of hot spot to nonhot spot   41:53   25:38   .62   <.0001  
Ratio of R to S  58:36   52:11   .0052   
R (ratio of C to F)  26:32   19:33   .38   .0011  
Mutations (ratio of C to F)   40:54   21:42   .25   .0005  
F (ratio of R to S)§  32:22  33:9  .045   
C (ratio R to S)§
 
26:14
 
19:2
 
.032
 

 

Parameter

Productive sequences

Nonproductive sequences

P (productive vs nonproductive)

P (targeted productive vs random)*
Mutations   94   63   .93   
Ratio of hot spot to nonhot spot   41:53   25:38   .62   <.0001  
Ratio of R to S  58:36   52:11   .0052   
R (ratio of C to F)  26:32   19:33   .38   .0011  
Mutations (ratio of C to F)   40:54   21:42   .25   .0005  
F (ratio of R to S)§  32:22  33:9  .045   
C (ratio R to S)§
 
26:14
 
19:2
 
.032
 

 

S107 sequences were cloned from the PCR product derived from sorted B220+ IgM IgD κ+ spleen cells pooled from 2 VavP-Bcl2 mice. For productive sequences, n = 14; for nonproductive sequences, n = 9.

*

Tests of whether mutations in productive sequences were significantly concentrated in the 36-base hot spots and 72-base C regions of the 300-base length analyzed

Replacement (R) vs silent (S) mutations

Replacement mutations in complementarity-determining (C) vs framework (F) regions

§

Replacement vs silent mutations in F and C regions, respectively

Ratios of replacement to silent mutations were not significantly different between C and F regions in productive (P = .57) or nonproductive (P = .24) sequences

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