Origin and evolutionary malleability of T cell receptor α diversity

Lymphocytes of vertebrate adaptive immune systems acquired the capability to assemble, from split genes in the germline, billions of functional antigen receptors(1-3). These receptors show specificity; unlike the broadly tuned receptors of the innate system, antibodies (Ig) expressed by B cells, for instance, can accurately distinguish between the two enantiomers of organic acids(4), whereas T cell receptors (TCRs) reliably recognize single amino acid replacements in their peptide antigens(5). In developing lymphocytes, antigen receptor genes are assembled from a comparatively small set of germline-encoded genetic elements in a process referred to as V(D)J recombination(6,7). Potential self-reactivity of some antigen receptors arising from the quasi-random somatic diversification is suppressed by several robust control mechanisms(8-12). For decades, scientists have puzzled over the evolutionary origin of somatically diversifying antigen receptors(13-16). It has remained unclear how, at the inception of this mechanism, immunologically beneficial expanded receptor diversity was traded against the emerging risk of destructive self-recognition. Here we explore the hypothesis that in early vertebrates, sequence microhomologies marking the ends of recombining elements became the crucial targets of selection determining the outcome of non-homologous end joining-based repair of DNA double-strand breaks generated during RAG-mediated recombination. We find that, across the main clades of jawed vertebrates, TCRa repertoire diversity is best explained by species-specific extents of such sequence microhomologies. Thus, selection of germline sequence composition of rearranging elements emerges as a major factor determining the degree of diversity of somatically generated antigen receptors.

Automated summary

Lymphocytes of vertebrate adaptive immune systems can assemble billions of functional antigen receptors from split genes in the germline. These receptors show specificity and can distinguish between different molecules. The diversity of the TCRa repertoire in different vertebrate species can be explained by the extent of sequence microhomologies marking the ends of recombining elements.