Table 1

VH gene analysis of murine gastric MALT lymphoma cases

CaseVH segmentHomology %Clones sequencedSomatic* mutationFR/CDRRSAntigen selectionPIntraclonal variationCDR3 length
mu-1 IGHV1-S130*01 93.06 11 FR 42 − .490 11 
     CDR 29 .000   
mu-2 IGHV14-3*02 92.36 10 FR 13 − .391 15 
     CDR .059   
mu-3 IGHV1-S81*02 97.92 13 FR .562 − 13 
     CDR − .801   
mu-4 IGHV14-3*02 99.31 10 − FR .000 13 
     CDR − .621   
mu-5 IGHV1-69*02 86.46 FR 24 − .491 − 10 
     CDR − .601   
mu-6 IGHV1-67*1 80.90 10 FR .03 − 12 
     CDR − .110   
mu-7 IGHV1-S22*01 94.62 22 FR − .112 − 15 
     CDR − .009   
mu-8 IGHV14-3*02 98.61 − FR .329 11 
     CDR − 1.278   
mu-9 IGHV1-18*02 88.19 FR 18 10 .107 12 
     CDR .369   
mu-10 IGHV1-S81*02 95.83 10 FR − .23 14 
     CDR − .156   
mu-11 IGHV1-74*01 86.81 10 FR 17 .12 − 12 
     CDR 10 .034   
CaseVH segmentHomology %Clones sequencedSomatic* mutationFR/CDRRSAntigen selectionPIntraclonal variationCDR3 length
mu-1 IGHV1-S130*01 93.06 11 FR 42 − .490 11 
     CDR 29 .000   
mu-2 IGHV14-3*02 92.36 10 FR 13 − .391 15 
     CDR .059   
mu-3 IGHV1-S81*02 97.92 13 FR .562 − 13 
     CDR − .801   
mu-4 IGHV14-3*02 99.31 10 − FR .000 13 
     CDR − .621   
mu-5 IGHV1-69*02 86.46 FR 24 − .491 − 10 
     CDR − .601   
mu-6 IGHV1-67*1 80.90 10 FR .03 − 12 
     CDR − .110   
mu-7 IGHV1-S22*01 94.62 22 FR − .112 − 15 
     CDR − .009   
mu-8 IGHV14-3*02 98.61 − FR .329 11 
     CDR − 1.278   
mu-9 IGHV1-18*02 88.19 FR 18 10 .107 12 
     CDR .369   
mu-10 IGHV1-S81*02 95.83 10 FR − .23 14 
     CDR − .156   
mu-11 IGHV1-74*01 86.81 10 FR 17 .12 − 12 
     CDR 10 .034   

MALT indicates mucosa-associated lymphoid tissue; FR, framework region; CDR, complementary determining region; R, replacement; S, silent; and mu, murine.

*

VH gene sequences deviating more than 2% from the corresponding germline gene were defined as somatically mutated.

Presence or absence of positive selection by antigen in the CDR is denoted by + and −, respectively. Presence or absence of negative selection by antigen in the FR is denoted by + and −, respectively, based on the cutoff ratio of 2.9 for replacement to silent mutations.

The P value was calculated based on the multinomial distribution model and is the probability that excess (for CDR) or scarcity (for FR) of mutations occurred by chance.

or Create an Account

Close Modal
Close Modal