Two Successive Inversional Vβ Rearrangements on a Single Tcrb Allele Can Contribute to the TCRβ Repertoire

• Published in: The Journal of immunology (1950) 2020-01, Vol.204 (1), p.78-86
• Main Authors: Lee, Kyutae D, Bassing, Craig H
• Format: Article
• Language: English
• Subjects: Alleles; Animals; Genes, T-Cell Receptor beta - genetics; Genes, T-Cell Receptor beta - immunology; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; T-Lymphocytes - immunology
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.1901105

Mammalian TCRβ loci contain 30 Vβ gene segments upstream and in the same transcriptional orientation as two DJCβ clusters, and a downstream Vβ (TRBV31) in the opposite orientation. The textbook view is upstream Vβs rearrange only by deletion and TRBV31 rearranges only by inversion to create VβDJCβ genes. In this study, we show in mice that upstream Vβs recombine through inversion to the DJCβ2 cluster on alleles carrying a preassembled -DJCβ1 gene. When this gene is in-frame, evades TCRβ-signaled feedback inhibition and recombines by inversion to the DJCβ2 cluster, creating αβ T cells that express assembled -DJCβ2 genes. On alleles with an out-of-frame -DJCβ1 gene, most upstream Vβs recombine at low levels and promote αβ T cell development, albeit with preferential expansion of -DJβ2 rearrangements. Finally, we show wild-type alleles produce mature αβ T cells that express upstream Vβ peptides in surface TCRs and carry -DJβ2 rearrangements. Our study indicates two successive inversional Vβ-to-DJβ rearrangements on the same allele can contribute to the TCRβ repertoire.