| Literature DB >> 29594415 |
Rebecca A Morgan1, Julie A Karl2, Hailey E Bussan2, Katelyn E Heimbruch1, David H O'Connor1,2, Dawn M Dudley3.
Abstract
Baboons are valuable models for complex human diseases due to their genetic and physiologic similarities to humans. Deep sequencing methods to characterize full-length major histocompatibility complex (MHC) class I (MHC-I) alleles in different nonhuman primate populations were used to identify novel MHC-I alleles in baboons. We combined data from Illumina MiSeq sequencing and Roche/454 sequencing to characterize novel full-length MHC-I transcripts in a cohort of olive and hybrid olive/yellow baboons from the Southwest National Primate Research Center (SNPRC). We characterized 57 novel full-length alleles from 24 baboons and found limited genetic diversity at the MHC-I A locus, with significant sharing of two MHC-I A lineages between 22 out of the 24 animals characterized. These shared alleles provide the basis for development of tools such as MHC:peptide tetramers for studying cellular immune responses in this important animal model.Entities:
Keywords: Baboon; Illumina MiSeq sequencing; Major histocompatibility complex I; Papio anubis; Papio anubis cynocephalus; Papio hamadryas; Roche/454 pyrosequencing
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Year: 2018 PMID: 29594415 PMCID: PMC8130456 DOI: 10.1007/s00251-018-1057-3
Source DB: PubMed Journal: Immunogenetics ISSN: 0093-7711 Impact factor: 2.846