文献类型: 外文期刊
第一作者: Guo, Yongchen
作者: Guo, Yongchen;Hu, Xiaoxiang;Meng, Qingyong;Ren, Liming;Li, Ning;Zhao, Yaofeng;Bao, Yonghua;Meng, Qingwen;Zhao, Yaofeng
作者机构:
期刊名称:PLOS ONE ( 影响因子:3.24; 五年影响因子:3.788 )
ISSN: 1932-6203
年卷期: 2012 年 7 卷 6 期
页码:
收录情况: SCI
摘要: In science, the guinea pig is known as one of the gold standards for modeling human disease. It is especially important as a molecular and cellular biology model for studying the human immune system, as its immunological genes are more similar to human genes than are those of mice. The utility of the guinea pig as a model organism can be further enhanced by further characterization of the genes encoding components of the immune system. Here, we report the genomic organization of the guinea pig immunoglobulin (Ig) heavy and light chain genes. The guinea pig IgH locus is located in genomic scaffolds 54 and 75, and spans approximately 6,480 kb. 507 V-H segments (94 potentially functional genes and 413 pseudogenes), 41 D-H segments, six J(H) segments, four constant region genes (mu, gamma, epsilon, and alpha), and one reverse delta remnant fragment were identified within the two scaffolds. Many V-H pseudogenes were found within the guinea pig, and likely constituted a potential donor pool for gene conversion during evolution. The Ig kappa locus mapped to a 4,029 kb region of scaffold 37 and 24 is composed of 349 V-kappa (111 potentially functional genes and 238 pseudogenes), three J(kappa) and one C-kappa genes. The Ig lambda locus spans 1,642 kb in scaffold 4 and consists of 142 V-lambda (58 potentially functional genes and 84 pseudogenes) and 11 J(lambda)-C-lambda clusters. Phylogenetic analysis suggested the guinea pig's large germline V-H gene segments appear to form limited gene families. Therefore, this species may generate antibody diversity via a gene conversion-like mechanism associated with its pseudogene reserves.
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