Human Genetics

, Volume 109, Issue 3, pp 253–261

Extent of linkage disequilibrium between the androgen receptor gene CAG and GGC repeats in human populations: implications for prostate cancer risk

Authors

  • Rick A. Kittles
    • National Human Genome Center, Howard University, 2041 Georgia Ave., Washington, DC 20060
  • Dale Young
    • National Human Genome Center, Howard University, 2041 Georgia Ave., Washington, DC 20060
  • Sally Weinrich
    • Population Studies, South Carolina Cancer Center, University of South Carolina, Columbia, SC 29203, USA
  • Julie Hudson
    • Population Studies, South Carolina Cancer Center, University of South Carolina, Columbia, SC 29203, USA
  • George Argyropoulos
    • Department of Medicine/Endocrinology, Medical University of South Carolina, Charleston, SC 29403, USA
  • Flora Ukoli
    • Cancer Center, Howard University, Washington, DC 20059, USA
  • Lucile Adams-Campbell
    • Cancer Center, Howard University, Washington, DC 20059, USA
  • Georgia M. Dunston
    • National Human Genome Center, Howard University, 2041 Georgia Ave., Washington, DC 20060
Original Investigation

DOI: 10.1007/s004390100576

Cite this article as:
Kittles, R.A., Young, D., Weinrich, S. et al. Hum Genet (2001) 109: 253. doi:10.1007/s004390100576

Abstract

While studies have implicated alleles at the CAG and GGC trinucleotide repeats of the androgen receptor gene with high-grade, aggressive prostate cancer disease, little is known about the normal range of variation for these two loci, which are separated by about 1.1 kb. More importantly, few data exist on the extent of linkage disequilibrium (LD) between the two loci in different human populations. Here we present data on CAG and GGC allelic variation and LD in six diverse populations. Alleles at the CAG and GGC repeat loci of the androgen receptor were typed in over 1000 chromosomes from Africa, Asia, and North America. Levels of linkage disequilibrium between the two loci were compared between populations. Haplotype variation and diversity were estimated for each population. Our results reveal that populations of African descent possess significantly shorter alleles for the two loci than non-African populations (P<0.0001). Allelic diversity for both markers was higher among African Americans than any other population, including indigenous Africans from Sierra Leone and Nigeria. Analysis of molecular variance revealed that approx. 20% of CAG and GGC repeat variance could be attributed to differences between the populations. All non-African populations possessed the same common haplotype while the three populations of African descent possessed three divergent common haplotypes. Significant LD was observed in our sample of healthy African Americans. The LD observed in the African American population may be due to several reasons; recent migration of African Americans from diverse rural communities following urbanization, recurrent gene flow from diverse West African populations, and admixture with European Americans. This study represents the largest genotyping effort to be performed on the two androgen receptor trinucleotide repeat loci in diverse human populations.

Copyright information

© Springer-Verlag 2001