Skip to main content
. Author manuscript; available in PMC: 2009 Aug 15.
Published in final edited form as: J Immunol. 2008 Aug 15;181(4):2556–2562. doi: 10.4049/jimmunol.181.4.2556

Table IV.

A comparison of the production mechanisms of public DbNP366-specific CDR3β amino acid sequences with and without N-addition.

CDR3βregion Minimum no. of required n- additions No. of recombination mechanisms
Without N- additions With N- additions
S G G A N T G Q L 40
130
agt ggg ggg gca aac acc ggg cag ctc 0 14
agt ggg ggc gca aac acc ggg cag ctc 0 12
agt ggg ggt gca aac acc ggg cag ctc 0 11
agt ggg ggg gcg aac acc ggg cag ctc 0 3
S G G G N T G Q L 2
80
agt ggg ggg gga aac acc ggg cag ctc 0 1
agt ggg ggg ggc aac acc ggg cag ctc 0 1
S G G S N T G Q L 0
60
agt ggg ggg tca aac acc ggg cag ctc 1
agt ggg ggc tca aac acc ggg cag ctc 1

Germline genes:
 Vβ 8.3: agt gat g, Jβ2S2: t gca aac acc ggg cag ctc
 Dβ 1: gggacagggggcg, D β2: gggactgggggggcg
a

Shown are the nucleotide sequences that encode commonly public DbNP366-specific CDR3β amino acid sequences and require a minimal number of N-additions to be produced. One possible V(D)J recombination mechanism is shown for each nucleotide sequence, with the nucleotides attributed by the germline Vβ, Dβ and Jβ genes shown in blue, red, and green, respectively. N-additions are shown in black and p-additions are shown in bold text. The number of possible recombination mechanisms that can produce these TCR sequences with no N-additions are shown. These different recombination mechanisms involve different splicings of the germline TCR genes and different p-additions (see Ref. 9 for more detail on different recombination mechanisms). Also shown is the number of different recombination mechanisms allowing for N-additions, determined from a simulation of a random V(D)J recombination process in which one million in-frame TCR sequences were generated (9).