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Data on the nucleotide composition of the first codons encoding the complementary determining region 3 (CDR3) in
Linnea Thörnqvist1, Mats Ohlin1
1Dept. of Immunotechnology, Lund University, Lund, Sweden.
Data in Brief
|June 13, 2018
Summary
The nucleotide composition of antibody CDR3 sequences reveals the extent of immunoglobulin heavy chain variable (IGHV) gene contribution to antibody diversity. This analysis impacts understanding antibody gene inference and specificity.
Area of Science:
- Immunology
- Genetics
- Bioinformatics
Background:
- The complementary determining region 3 (CDR3) of antibodies is crucial for antigen binding and exhibits high variability.
- This variability arises from the recombination of immunoglobulin heavy chain variable (IGHV), diversity (D), and joining (J) genes during B cell development.
Purpose of the Study:
- To analyze the nucleotide composition of codons encoding the initial residues of CDR3.
- To assess the contribution of the IGHV germline gene to CDR3 diversity and antibody specificity.
Main Methods:
- Analysis of nucleotide composition from two independent sets of antibody heavy chain-encoding transcript sequences.
- Utilized raw sequence data from allergic subjects and memory B cells, including paired heavy and light chain transcripts.
- Examined transcripts originating from 47 distinct IGHV alleles.
Main Results:
- Presented nucleotide compositions of the 5'-ends of CDR3-encoding sequences for various IGHV alleles.
- Demonstrated the extent of incorporation of 3' IGHV germline gene bases into rearranged immunoglobulin sequences.
- Assessed how IGHV gene differences affect CDR3 sequence composition and antibody specificity.
Conclusions:
- The nucleotide composition of CDR3 provides insights into IGHV gene contribution to antibody repertoire diversity.
- Understanding these sequence patterns is vital for accurate inference of IGHV gene usage and for predicting antibody specificity.
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