Genetic Polymorphism and Recombination in the Subtelomeric Region of Chromosome 14q |
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| Authors: | Richard F. Wintle,Torbjoern G. Nygaard,Jo-Anne S. Herbrick,Kirsti Kvalø y,Diane W. Cox |
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| Affiliation: | aResearch Institute, The Hospital For Sick Children, Toronto, Ontario, Canada;bDepartment of Molecular and Medical Genetics, the University of Toronto, Ontario, Canada;cDepartment of Neurology, Columbia University, New York, New York, 10027;eDepartment of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada;dNorwegian Institute for Nature Research, Trondheim, Norway |
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| Abstract: | Subtelomeric regions of human chromosomes are the sites of increased meiotic recombination and have a male-to-female recombination ratio that is higher than elsewhere in the genome. We isolated two novel, polymorphic CA repeat markers from the distal part of the immunoglobulin heavy chain gene cluster, approximately 90 and 200 kb from the telomere of chromosome 14q. The 14q telomere was unambiguously located by physical mapping of telomeric YACs andBal31 exonuclease digestion of genomic DNA. We then constructed haplotypes using genotype data from these markers and data from sCAW1 (D14S826) for use as a highly polymorphic genetic marker. Linkage analysis using the 40 pedigree CEPH reference panel and genotype data from these and other loci physically mapped to the terminal 1.5 Mb of chromosome 14q revealed an apparent increase in meiotic recombination within this region, relative to the average rate for the genome. Further, we found that recombination was higher in females than in males, indicating that the subtelomeric region of 14q differs from other human subtelomeric regions. |
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