Table1.

IgH CDR3 of Tet2-deficient CD19+B220low B cells reveals CLL-like features

MouseTagTet2 genotypeVDJCDR3Length, ntD reading frameIP
Tet2 ANO mice C12 ANO/WT V1-9 D-FL 16.2 J1 C AR SYYGYS WYFDV13 6,14 
ANO/WT V2-2 D-FL 16.3 J4 C AR KTNEVNYYDMDY14 4,72 
Tet2 CD19-Cre mice G212 Flox/WT V1-55 D-FL 16.1 J1 C AR IYYGSSYWYFDV14 6,14 
G203 Flox/WT V3-2 D-SP2.2 J4 C ARYYDYDYYAMDY13 4,15 
G322 Flox/WT V5-2 D-FL 16.1 J4 C ARLWYYVG YAMDY13 6,14 
G328 Flox/WT V3-6 D-SP2.9 J4 C AR DDGYYGD YAMDY14 3,99 
G211 Flox/flox V3-6 D-SP2.5 J4 C A NYGNYIS YAMDY13 3,75 
G200 Flox/flox V3-6 D-SP2.2 J4 C S TCPYDYDGS YYAMDY16 3,46 
G635 Flox/flox V2-2 D-FL 16.1 J4 C AR TPPYITTVVA PYAMDY18 6,14 
G630 Flox/flox V5-15 D-FL 16.1 J4 C AR HGGS AMDY10 7,17 
G103 Flox/flox V10-1 D-Q52 J2 C VR HDWDG FDY10 4,71 
G213 Flox/flox V5-9-1 D-SP2.5 J2 C TR EYLGSTTVPTIL DY16 4,44 
MouseTagTet2 genotypeVDJCDR3Length, ntD reading frameIP
Tet2 ANO mice C12 ANO/WT V1-9 D-FL 16.2 J1 C AR SYYGYS WYFDV13 6,14 
ANO/WT V2-2 D-FL 16.3 J4 C AR KTNEVNYYDMDY14 4,72 
Tet2 CD19-Cre mice G212 Flox/WT V1-55 D-FL 16.1 J1 C AR IYYGSSYWYFDV14 6,14 
G203 Flox/WT V3-2 D-SP2.2 J4 C ARYYDYDYYAMDY13 4,15 
G322 Flox/WT V5-2 D-FL 16.1 J4 C ARLWYYVG YAMDY13 6,14 
G328 Flox/WT V3-6 D-SP2.9 J4 C AR DDGYYGD YAMDY14 3,99 
G211 Flox/flox V3-6 D-SP2.5 J4 C A NYGNYIS YAMDY13 3,75 
G200 Flox/flox V3-6 D-SP2.2 J4 C S TCPYDYDGS YYAMDY16 3,46 
G635 Flox/flox V2-2 D-FL 16.1 J4 C AR TPPYITTVVA PYAMDY18 6,14 
G630 Flox/flox V5-15 D-FL 16.1 J4 C AR HGGS AMDY10 7,17 
G103 Flox/flox V10-1 D-Q52 J2 C VR HDWDG FDY10 4,71 
G213 Flox/flox V5-9-1 D-SP2.5 J2 C TR EYLGSTTVPTIL DY16 4,44 

Sequence analysis of PCR products obtained from GeneScan analysis was down using the JH primer. Results obtained were subject to analysis using IMGT/Vquest and IgBlast software to define all V, D, and J genes, as well as the CDR3 sequence. Columns show the identified IgH-V, -D, and -J genes; the resulting CDR3 sequence, the CDR3 length; the D genes reading frame, and the isoelectric point (IP) of the CDR3. The background of the mice that developed the abnormal B-cell population is indicated. 2 abnormal populations heterozygous for Tet2 gene-trap model (Tet2LacZ ANO) are shown, as well as 4 heterozygous Tet2 floxed alleles (Tet2−/+) and 6 homozygous inactivated Tet2 (Tet2−/−) in CD19-Cre Tet2 background. The last 3 lines represent analysis of 3 abnormal Tet2 populations that have emerged in 3 secondary recipients engrafted from the same primary Tet2CD19-Cre+ mice. In the “CDR3” column, amino acid residues encoded by the V or J segments (underlined) are separated by spaces from those encoded by the D segment (in bold and underlined).

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