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Cytidine deaminase 2 is required for VLRB antibody gene assembly in lampreys
Department of Developmental Immunology, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.ORCID-id: 0000-0002-5497-4666
Department of Developmental Immunology, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Department of Developmental Immunology, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
Department of Developmental Immunology, Max Planck Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany.
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2020 (engelsk)Inngår i: Science immunology, E-ISSN 2470-9468, Vol. 5, nr 45, artikkel-id eaba0925Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The antibodies of jawless vertebrates consist of leucine-rich repeat arrays encoded by somatically assembled VLRB genes. It is unknown how the incomplete germline VLRB loci are converted into functional antibody genes during B lymphocyte development in lampreys. In Lampetra planeri larvae lacking the cytidine deaminase CDA2 gene, VLRB assembly fails, whereas the T lineage–associated VLRA and VLRC antigen receptor gene assemblies occur normally. Thus, CDA2 acts in a B cell lineage–specific fashion to support the somatic diversification of VLRB antibody genes. CDA2 is closely related to activation-induced cytidine deaminase (AID), which is essential for the elaboration of immunoglobulin gene repertoires in jawed vertebrates. Our results thus identify a convergent mechanism of antigen receptor gene assembly and diversification that independently evolved in the two sister branches of vertebrates.

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American Association for the Advancement of Science (AAAS), 2020. Vol. 5, nr 45, artikkel-id eaba0925
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URN: urn:nbn:se:umu:diva-231206DOI: 10.1126/sciimmunol.aba0925ISI: 000523594100007PubMedID: 32169953Scopus ID: 2-s2.0-85081954277OAI: oai:DiVA.org:umu-231206DiVA, id: diva2:1908301
Tilgjengelig fra: 2024-10-25 Laget: 2024-10-25 Sist oppdatert: 2024-10-28bibliografisk kontrollert

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