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Complete Genomic Assembly of Mauritian Cynomolgus Macaque Killer Ig-like Receptor and Natural Killer Group 2 Haplotypes.
Prall, Trent M; Karl, Julie A; Varghese, Joshua M; Baker, David A; Minor, Nicholas R; Raveendran, Muthuswamy; Harris, R Alan; Rogers, Jeffery; Wiseman, Roger W; O'Connor, David H.
Afiliación
  • Prall TM; Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI.
  • Karl JA; Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI.
  • Varghese JM; Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI.
  • Baker DA; Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI.
  • Minor NR; Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI.
  • Raveendran M; Human Genome Sequencing Center and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
  • Harris RA; Human Genome Sequencing Center and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
  • Rogers J; Human Genome Sequencing Center and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
  • Wiseman RW; Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI.
  • O'Connor DH; Wisconsin National Primate Research Center, University of Wisconsin-Madison, Madison, WI.
J Immunol ; 212(11): 1754-1765, 2024 Jun 01.
Article en En | MEDLINE | ID: mdl-38639635
ABSTRACT
Mauritian-origin cynomolgus macaques (MCMs) serve as a powerful nonhuman primate model in biomedical research due to their unique genetic homogeneity, which simplifies experimental designs. Despite their extensive use, a comprehensive understanding of crucial immune-regulating gene families, particularly killer Ig-like receptors (KIR) and NK group 2 (NKG2), has been hindered by the lack of detailed genomic reference assemblies. In this study, we employ advanced long-read sequencing techniques to completely assemble eight KIR and seven NKG2 genomic haplotypes, providing an extensive insight into the structural and allelic diversity of these immunoregulatory gene clusters. Leveraging these genomic resources, we prototype a strategy for genotyping KIR and NKG2 using short-read, whole-exome capture data, illustrating the potential for cost-effective multilocus genotyping at colony scale. These results mark a significant enhancement for biomedical research in MCMs and underscore the feasibility of broad-scale genetic investigations.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Haplotipos / Receptores KIR / Macaca fascicularis Límite: Animals Idioma: En Revista: J Immunol Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Haplotipos / Receptores KIR / Macaca fascicularis Límite: Animals Idioma: En Revista: J Immunol Año: 2024 Tipo del documento: Article