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Title: Linkage disequilibrium patterns vary with chromosomal location: A case study from the von Willebrand factor region

Journal Article · · American Journal of Human Genetics; (United States)
OSTI ID:6811015
; ; ;  [1];  [2];  [3];
  1. Univ. of Utah School of Medicine, Salt Lake City, UT (United States)
  2. Aland Central Sjukhus (Finland)
  3. Free Univ., Amsterdam (Netherlands)

Linkage disequilibrium analysis has been used as a tool for analyzing marker order and locating disease genes. Under appropriate circumstances, disequilibrium patterns reflect recombination events that have occurred throughput a population's history. As a result, disequilibrium mapping may be useful in genomic regions of <1 cM where the number of informative meioses needed to detect recombinant individuals within pedigrees is exceptionally high. Its utility for refining target areas for candidate disease genes before initiating chromosomal walks and cloning experiments will be enhanced as the relationship between linkage disequilibrium and physical distance is better understood. To address this issue, the authors have characterized linkage disequilibrium in a 144-kb region of the von Willebrand factor gene on chromosome 12. Sixty CEPH and 12 von Willebrand disease families were genotypes for five PCR-based markers, which include two microsatellite repeats and three single-base-pair substitutions. Linkage disequilibrium and physical distance between polymorphisms are highly correlated (r[sub m] = -.76; P<.05) within this region. None of the five markers showed significant disequilibrium with the von Willebrand disease phenotype. The linkage disequilibrium/physical distance relationship was also analyzed as a function of chromosomal location for this and eight previously characterized regions. This analysis revealed a general trend in which linkage disequilibrium dissipates more rapidly with physical distance in telomeric regions than in centromeric regions. This trend is consistent with higher recombination rates near telomeres. 52 refs., 3 figs., 4 tabs.

OSTI ID:
6811015
Journal Information:
American Journal of Human Genetics; (United States), Vol. 55:2; ISSN 0002-9297
Country of Publication:
United States
Language:
English