Rapid Evolution of Major Histocompatibility Complex Class I Genes in Primates Generates New Disease Alleles in Humans via Hitchhiking Diversity

A plausible explanation for many MHC-linked diseases is lacking. Sequencing of the MHC class I region (coding units or full contigs) in several human and nonhuman primate haplotypes allowed an analysis of single nucleotide variations (SNV) across this entire segment. This diversity was not evenly di...

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Main Authors: Shiina, Takashi, Ota, Masao, Shimizu, Sayoko, Katsuyama, Yoshihiko, Hashimoto, Nami, Takasu, Miwa, Anzai, Tatsuya, Kulski, Jerzy K., Kikkawa, Eri, Naruse, Taeko, Kimura, Natsuki, Yanagiya, Kazuyo, Watanabe, Atsushi, Hosomichi, Kazuyoshi, Kohara, Sakae, Iwamoto, Chie, Umehara, Yumi, Meyer, Alice, Wanner, Valérie, Sano, Kazumi, Macquin, Cécile, Ikeo, Kazuho, Tokunaga, Katsushi, Gojobori, Takashi, Inoko, Hidetoshi, Bahram, Seiamak
Formato: Artigo
Idioma:Inglês
Publicado em: Copyright © 2006 by the Genetics Society of America 2006
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Investigations
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1526686/
https://ncbi.nlm.nih.gov/pubmed/16702430
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.106.057034
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