Origin and evolutionary malleability of T cell receptor α diversity

Orlando B. Giorgetti (), Connor P. O’Meara, Michael Schorpp and Thomas Boehm ()
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Orlando B. Giorgetti: Max Planck Institute of Immunobiology and Epigenetics
Connor P. O’Meara: Max Planck Institute of Immunobiology and Epigenetics
Michael Schorpp: Max Planck Institute of Immunobiology and Epigenetics
Thomas Boehm: Max Planck Institute of Immunobiology and Epigenetics

Nature, 2023, vol. 619, issue 7968, 193-200

Abstract: Abstract Lymphocytes of vertebrate adaptive immune systems acquired the capability to assemble, from split genes in the germline, billions of functional antigen receptors1–3. 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 acids4, whereas T cell receptors (TCRs) reliably recognize single amino acid replacements in their peptide antigens5. 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 recombination6,7. Potential self-reactivity of some antigen receptors arising from the quasi-random somatic diversification is suppressed by several robust control mechanisms8–12. For decades, scientists have puzzled over the evolutionary origin of somatically diversifying antigen receptors13–16. 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, TCRα 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.

Date: 2023
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DOI: 10.1038/s41586-023-06218-x

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