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Genetic conflicts and the origin of self/nonself-discrimination in the vertebrate immune system
Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany; Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.ORCID iD: 0000-0002-5497-4666
Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.
Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.
2023 (English)In: Trends in Immunology, Vol. 44, no 5, p. 372-383Article, review/survey (Refereed) Published
Abstract [en]

Genetic conflicts shape the genomes of prokaryotic and eukaryotic organisms. Here, we argue that some of the key evolutionary novelties of adaptive immune systems of vertebrates are descendants of prokaryotic toxin-antitoxin (TA) systems. Cytidine deaminases and RAG recombinase have evolved from genotoxic enzymes to programmable editors of host genomes, supporting the astounding discriminatory capability of variable lymphocyte receptors of jawless vertebrates, as well as immunoglobulins and T cell receptors of jawed vertebrates. The evolutionarily recent lymphoid lineage is uniquely sensitive to mutations of the DNA maintenance methylase, which is an orphaned distant relative of prokaryotic restriction-modification systems. We discuss how the emergence of adaptive immunity gave rise to higher order genetic conflicts between genetic parasites and their vertebrate host.

Place, publisher, year, edition, pages
Elsevier, 2023. Vol. 44, no 5, p. 372-383
Keywords [en]
RAG recombinase, antigen receptor diversity, cytidine deaminase, evolution, genetic conflict.
National Category
Immunology
Identifiers
URN: urn:nbn:se:umu:diva-231202DOI: 10.1016/j.it.2023.02.007ISI: 000989168500001PubMedID: 36941153Scopus ID: 2-s2.0-85150260601OAI: oai:DiVA.org:umu-231202DiVA, id: diva2:1908307
Available from: 2024-10-25 Created: 2024-10-25 Last updated: 2024-10-25Bibliographically approved

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Morimoto, Ryo

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