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Duplications and deletions of the human IGHC locus: evolutionary implications
Authors:H Rabbani  Qiang Pan  Naomi Kondo  C I Edvard Smith  Lennart Hammarström
Institution:(1) Department of Bioscience at Novum, Karolinska Institute, S-141 57 Huddinge, Sweden, SE;(2) Department of Pediatrics, Gifu University School of Medicine, Tsukasa-Machi 40, Gifu 500, Japan, JP
Abstract: A limited number of deletions and duplications within the human immunoglobulin heavy chain constant locus (IGHC) has previously been reported. We studied the IGHC locus in about 500 individuals representing three major races of human, Negroid (Gambian), Mongoloid (Japanese and Chinese), and Caucasoid (Iranian and Swedish). The haplotype frequency of duplications is highest in the Mongoloid population (22%), followed by the Caucasian (10%) and Negroid (5%) populations. The corresponding frequency of deletions are 2, 1.5, and 3.5%, respectively. New types of multiple duplications were found in this study on different genetic (H haplotype and racial) backgrounds. The most common duplication, found in all populations studied, encompasses the IGHA1-IGHE genes. The only deletion common to all racial groups is an isolated deletion of the IGHG4 gene. Our data are consistent with the hypothesis that the Caucasoid-Mongoloid group diverged from the hominoid ancestor after development of the Negroid populations, with subsequent evolution within the respective groups thereafter. Received: 14 June 1996/Revised: 2 August 1996
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