Gene mapping in isolated populations: new roles for old friends?
- PMID: 10545758
- DOI: 10.1159/000022891
Gene mapping in isolated populations: new roles for old friends?
Abstract
Population isolates are increasingly being used in attempts to map genes underlying complex diseases. To further explore the utility of isolates for this purpose, we explore linkage disequilibrium patterns in polymorphisms from two regions (VWF and NF1) in three isolated populations from Finland. At the NF1 locus, the Finnish populations have greater pairwise disequilibrium than populations from Africa, Asia, or northern Europe. However, populations from 'New Finland' and 'Old Finland' do not differ in their disequilibrium levels at either the NF1 or the VWF locus. In addition, disequilibrium patterns and haplotype diversity do not differ between a sample from the Aland Islands, Finland, and a collection of outbred Centre d'Etude du Polymorphisme Humain families. These results show that linkage disequilibrium patterns sometimes differ among populations with different histories and founding dates, but some putative isolated populations may not significantly differ from larger admixed populations. We discuss factors that should be considered when using isolated populations in gene-mapping studies.
Similar articles
-
Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping.Am J Hum Genet. 1993 Nov;53(5):1038-50. Am J Hum Genet. 1993. PMID: 8105688 Free PMC article.
-
The genetically isolated populations of Finland and sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes.Nat Genet. 2000 Jul;25(3):320-3. doi: 10.1038/77091. Nat Genet. 2000. PMID: 10888882
-
Cosmopolitan linkage disequilibrium maps.Hum Genomics. 2005 Mar;2(1):20-7. doi: 10.1186/1479-7364-2-1-20. Hum Genomics. 2005. PMID: 15814065 Free PMC article.
-
A database of polymorphisms in the von Willebrand factor gene and pseudogene. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.Thromb Haemost. 1993 Feb 1;69(2):185-91. Thromb Haemost. 1993. PMID: 8456432 Review.
-
Molecular genetics of the Finnish disease heritage.Hum Mol Genet. 1999;8(10):1913-23. doi: 10.1093/hmg/8.10.1913. Hum Mol Genet. 1999. PMID: 10469845 Review.
Cited by
-
Molecular Epidemiology in Amerindians of the Brazilian Amazon Reveals New Genetic Variants in DNA Repair Genes.Genes (Basel). 2022 Oct 15;13(10):1869. doi: 10.3390/genes13101869. Genes (Basel). 2022. PMID: 36292754 Free PMC article.
-
Inter-individual genomic heterogeneity within European population isolates.PLoS One. 2019 Oct 9;14(10):e0214564. doi: 10.1371/journal.pone.0214564. eCollection 2019. PLoS One. 2019. PMID: 31596857 Free PMC article.
-
Overcoming the dichotomy between open and isolated populations using genomic data from a large European dataset.Sci Rep. 2017 Feb 1;7:41614. doi: 10.1038/srep41614. Sci Rep. 2017. PMID: 28145502 Free PMC article.
-
Association Between CHRNA3 and CHRNA5 Nicotine Receptor Subunit Gene Variants and Nicotine Dependence in an Isolated Populationof Kashubians in Poland.Med Sci Monit. 2016 Apr 29;22:1442-50. doi: 10.12659/msm.895907. Med Sci Monit. 2016. PMID: 27127891 Free PMC article.
-
Common polygenic variation contributes to risk of migraine in the Norfolk Island population.Hum Genet. 2015 Oct;134(10):1079-87. doi: 10.1007/s00439-015-1587-9. Epub 2015 Jul 29. Hum Genet. 2015. PMID: 26220684
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous