Abstract
VH replacement occurs through RAG-mediated recombination between the cryptic recombination signal sequence (cRSS) near the 3′ end of a rearranged VH gene and the 23-bp RSS from an upstream unrearranged VH gene. Due to the location of the cRSS, VH replacement leaves a short stretch of nucleotides from the previously rearranged VH gene at the newly formed V-D junction, which can be used as a marker to identify VH replacement products. To determine the contribution of VH replacement products to mouse antibody repertoire, we developed a Java-based VH Replacement Footprint Analyzer (VHRFA) program and analyzed 17,179 mouse IgH gene sequences from the NCBI database to identify VH replacement products. The overall frequency of VH replacement products in these IgH genes is 5.29% based on the identification of pentameric VH replacement footprints at their V-D junctions. The identified VH replacement products are distributed similarly in IgH genes using most families of VH genes, although different families of VH genes are used differentially. The frequencies of VH replacement products are significantly elevated in IgH genes derived from several strains of autoimmune prone mice and in IgH genes encoding autoantibodies. Moreover, the identified VH replacement footprints in IgH genes from autoimmune prone mice or IgH genes encoding autoantibodies preferentially encode positively charged amino acids. These results revealed a significant contribution of VH replacement products to the diversification of antibody repertoire and potentially, to the generation of autoantibodies in mice.
Highlights
The variable region exons of the immunoglobulin (Ig) genes are generated through sequential rearrangement of previously separated VH, DH, and JH gene segments catalyzed by the recombination activating gene products (RAG1 and RAG2) [1,2,3,4,5]
The Mouse Ig heavy (IgH) Sequence Repertoire To analyze a large number of IgH gene sequences and to identify potential VH replacement products, we developed a Java based VH Replacement Footprint Analyzer (VHRFA) program
This analysis represents a comprehensive view of the IgH repertoire of the current available mouse IgH gene sequences in the National Center for Biotechnology Information (NCBI) database
Summary
The variable region exons of the immunoglobulin (Ig) genes are generated through sequential rearrangement of previously separated VH, DH (for heavy chain only), and JH gene segments catalyzed by the recombination activating gene products (RAG1 and RAG2) [1,2,3,4,5]. The RSS consists of a highly conserved heptamer and a nonamer, separated by a non-conserved spacer region with either 12-bp or 23-bp nucleotides [6,7,8,9]. The coding end hairpins are opened and re-joined to form the coding exon of Ig gene, whereas the signal ends are ligated to form an excision circle and released from the chromosomal DNA [6,7]
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