Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene.

A genome-wide map of single nucleotide polymorphisms (SNP) and a pattern of linkage disequilibrium (LD) between their alleles are being established in three main ethnic groups. An important question is the applicability of such maps to different populations within a main ethnic group. Therefore, we have developed high-resolution SNP, haplotype and LD maps of vitamin D receptor gene region in large samples from five populations. Comparative analysis reveals that the LD patterns are identical in all four European populations tested with two small regions of 1.3 and 5.7 kb at which LD is disrupted completely resulting in three block-like regions over which there is significant and extensive LD. In an African population the pattern is similar, but two additional LD-breaking spots are also apparent. This LD pattern suggests combined action of recombination hotspots and founder effects, but cannot be explained by random recombination and genetic drift alone. Direct comparison indicates that the tag SNPs selected in one European population effectively predict the non-tag SNPs in the other Europeans, but not in the Gambians, for this region.

[1]  C. Stringer,et al.  Genetic and fossil evidence for the origin of modern humans. , 1988, Science.

[2]  G. Bertorelle,et al.  Genetics and the population history of Europe. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[3]  S. Gabriel,et al.  The Structure of Haplotype Blocks in the Human Genome , 2002, Science.

[4]  J. Pritchard,et al.  Linkage disequilibrium in humans: models and data. , 2001, American journal of human genetics.

[5]  Gonçalo R. Abecasis,et al.  GOLD-Graphical Overview of Linkage Disequilibrium , 2000, Bioinform..

[6]  M. Daly,et al.  High-resolution haplotype structure in the human genome , 2001, Nature Genetics.

[7]  M. Stoneking Mitochondrial DNA and human evolution , 1994, Journal of bioenergetics and biomembranes.

[8]  J. Akey,et al.  Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation. , 2002, American journal of human genetics.

[9]  Momiao Xiong,et al.  Randomly distributed crossovers may generate block-like patterns of linkage disequilibrium: an act of genetic drift , 2003, Human Genetics.

[10]  Benjamin Yakir,et al.  Linkage disequilibrium patterns of the human genome across populations. , 2003, Human molecular genetics.

[11]  B. J. Carey,et al.  Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots , 2003, Nature Genetics.

[12]  J. Shine,et al.  Cloning and expression of full-length cDNA encoding human vitamin D receptor. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[13]  S. Pääbo,et al.  Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[14]  A. Jeffreys,et al.  Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX , 2002, Nature Genetics.

[15]  P. Donnelly,et al.  The Fine-Scale Structure of Recombination Rate Variation in the Human Genome , 2004, Science.

[16]  R. Lewontin The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models. , 1964, Genetics.

[17]  Pardis C Sabeti,et al.  Linkage disequilibrium in the human genome , 2001, Nature.

[18]  Luc J. Smink,et al.  Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease , 2003, Nature.

[19]  D. Goldstein Islands of linkage disequilibrium , 2001, Nature Genetics.

[20]  H. DeLuca,et al.  Current understanding of the molecular actions of vitamin D. , 1998, Physiological reviews.

[21]  Gudmundur A. Thorisson,et al.  The International HapMap Project Web site. , 2005, Genome research.

[22]  A. Jeffreys,et al.  Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex , 2001, Nature Genetics.

[23]  A. Jeffreys,et al.  Recombination hotspots rather than population history dominate linkage disequilibrium in the MHC class II region. , 2003, Human molecular genetics.

[24]  Frank Dudbridge,et al.  Haplotype tagging for the identification of common disease genes , 2001, Nature Genetics.

[25]  J. Eisman,et al.  Multiple promoters direct the tissue-specific expression of novel N-terminal variant human vitamin D receptor gene transcripts. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[26]  J. Cauley,et al.  Molecular epidemiology of vitamin D receptor gene variants. , 2000, Epidemiologic reviews.

[27]  Kathryn F. Beal,et al.  The Staden package, 1998. , 2000, Methods in molecular biology.

[28]  Juliet M Chapman,et al.  Detecting Disease Associations due to Linkage Disequilibrium Using Haplotype Tags: A Class of Tests and the Determinants of Statistical Power , 2003, Human Heredity.

[29]  John A. Todd,et al.  The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes , 2000, Nature Genetics.