{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,7]],"date-time":"2026-03-07T16:53:36Z","timestamp":1772902416897,"version":"3.50.1"},"reference-count":30,"publisher":"Rockefeller University Press","issue":"6","content-domain":{"domain":["rupress.org"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2005,9,19]]},"abstract":"<jats:p>Class switch recombination was the last of the lymphocyte-specific DNA modification reactions to appear in the evolution of the adaptive immune system. It is absent in cartilaginous and bony fish, and it is common to all tetrapods. Class switching is initiated by activation-induced cytidine deaminase (AID), an enzyme expressed in cartilaginous and bony fish that is also required for somatic hypermutation. Fish AID differs from orthologs found in tetrapods in several respects, including its catalytic domain and carboxy-terminal region, both of which are essential for the switching reaction. To determine whether evolution of class switch recombination required alterations in AID, we assayed AID from Japanese puffer and zebra fish for class-switching activity in mouse B cells. We find that fish AID catalyzes class switch recombination in mammalian B cells. Thus, AID had the potential to catalyze this reaction before the teleost and tetrapod lineages diverged, suggesting that the later appearance of a class-switching reaction was dependent on the evolution of switch regions and multiple constant regions in the IgH locus.<\/jats:p>","DOI":"10.1084\/jem.20051378","type":"journal-article","created":{"date-parts":[[2005,9,12]],"date-time":"2005-09-12T20:33:27Z","timestamp":1126557207000},"page":"733-738","update-policy":"https:\/\/doi.org\/10.1084\/jem.crossmarkpolicy","source":"Crossref","is-referenced-by-count":93,"title":["AID from bony fish catalyzes class switch recombination"],"prefix":"10.1084","volume":"202","author":[{"given":"Vasco M.","family":"Barreto","sequence":"first","affiliation":[{"name":"1Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10021"}]},{"given":"Qiang","family":"Pan-Hammarstrom","sequence":"additional","affiliation":[{"name":"3Division of Clinical Immunology, F79, Department of Laboratory Medicine, Karolinska University Hospital, Huddinge, SE-141 86 Stockholm, Sweden"}]},{"given":"Yaofeng","family":"Zhao","sequence":"additional","affiliation":[{"name":"3Division of Clinical Immunology, F79, Department of Laboratory Medicine, Karolinska University Hospital, Huddinge, SE-141 86 Stockholm, Sweden"}]},{"given":"Lennart","family":"Hammarstrom","sequence":"additional","affiliation":[{"name":"3Division of Clinical Immunology, F79, Department of Laboratory Medicine, Karolinska University Hospital, Huddinge, SE-141 86 Stockholm, Sweden"}]},{"given":"Ziva","family":"Misulovin","sequence":"additional","affiliation":[{"name":"2Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10021"},{"name":"4Edward A. Doisy Department of Biochemistry and Molecular Biology, Health Sciences Center, Saint Louis University School of Medicine, St. Louis, MO 63104"}]},{"given":"Michel C.","family":"Nussenzweig","sequence":"additional","affiliation":[{"name":"1Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10021"},{"name":"2Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10021"}]}],"member":"291","published-online":{"date-parts":[[2005,9,12]]},"reference":[{"key":"2023072513203876400_BIB1","doi-asserted-by":"crossref","first-page":"688","DOI":"10.1038\/nri889","volume":"2","year":"2002","journal-title":"Nat. Rev. Immunol."},{"key":"2023072513203876400_BIB2","doi-asserted-by":"crossref","first-page":"5","DOI":"10.1111\/j.0105-2896.2004.00173.x","volume":"200","year":"2004","journal-title":"Immunol. 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