The increased utility of the rhesus macaque animal model in both HIV vaccine development and pathogenesis studies necessitates the development of a solid genetics and immunogeneticsdata infrastructure for this species. Relative to human data, there is a paucity of information about the larger-scale gene content of the macaqueMHC and very littlepolymorphism data from outsideof the macaque class I and I1 genes. As a pointed example, indirect evidence exists that there may be as many as 3 class I B loci and 2 class I A loci on certain macaque haplotypes, but this has not been confirmed through direct genomic analysis. Thus the number of actively expressed class I genes in an individual experimental macaque may be unknown. An essentially similar story underlies some class I1 loci, and very little structural data exists about the hundreds of other genes present in the macaque MHC, more than a third of which are also directly involved in the immuneresponse. These deficiencies provide substantial immediate motivation to better understand the genetics and immunogenetics of rhesus macaques that could be useful in the design and conduct of AIDS vaccine experiments in the simian immunodeficiency(SIV) and chimeric SIV-HIV(SHIV) animal models using this nonhuman primate species. Towards this end, we propose to develop a DNA sequenceof a macaque major histocompatibility complex (MHC)of finished high quality data. We further propose to annotatethis data string with extensivepolymorphism data (SNP) and larger-scale haplotypic variation, and with respect to the complete gene content of the region. One fundamental priority will be to effectively organize and disseminate this data to the interested scientific community. Todevelop this resource, we propose to accomplish the following specific aims: 1) To derive a complete and high quality genomic sequence of a major histocompatibility complex (MHC)from the rhesus macaque. 2) To develop and define a set of SNPs and larger scale haplotype structures useful as mapping tools in the association with MHC- linked phenotypes. 3) To identify and annotate genes and polymorphims in the macaque MHC and make this resource available in a useful and palatable form tothe scientific community. We will accomplish these aims in part by combining resources and expertise in macaque genetics,genomics, and function from three accomplished laboratories.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Resource-Related Research Projects (R24)
Project #
3R24RR017186-05S1
Application #
7478909
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Program Officer
Harding, John D
Project Start
2002-06-06
Project End
2008-04-30
Budget Start
2006-05-01
Budget End
2008-04-30
Support Year
5
Fiscal Year
2007
Total Cost
$610,917
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
City
Seattle
State
WA
Country
United States
Zip Code
98109
Daza-Vamenta, Riza; Glusman, Gustavo; Rowen, Lee et al. (2004) Genetic divergence of the rhesus macaque major histocompatibility complex. Genome Res 14:1501-15