Do delta F508 heterozygotes have a selective advantage?
- PMID: 11556136
- DOI: 10.1017/s0016672301005195
Do delta F508 heterozygotes have a selective advantage?
Abstract
In this paper the fitness of the delta F508 heterozygote is assessed and the age of the delta F508 mutation in the cystic fibrosis locus is estimated. Data from three microsatellite loci are applied. The analysis is performed conditional on the present-day frequency of the delta F508 mutation and based on assumptions about the demographic history of the European population and the mutation rate in the three microsatellite loci. It is shown that the data gives evidence of positive selection (up to 2-3% per delta F508 heterozygote), but also that data could be explained by negative selection of roughly the same order of magnitude. The age of the delta F508 mutation is subsequently estimated; it is found that the mutation is at least 580 generations old, but could be much older depending on the microsatellite mutation rate and the exact number of substitutions experienced in the history of the three microsatellite loci.
Similar articles
-
Microsatellite haplotypes of Polish cystic fibrosis alleles: delta F508 chromosomes demonstrate a North-South haplotype frequency gradient.Hum Hered. 1996 Nov-Dec;46(6):310-4. doi: 10.1159/000154370. Hum Hered. 1996. PMID: 8956026
-
An evolutionary approach to the high frequency of the Delta F508 CFTR mutation in European populations.Med Hypotheses. 2010 Jun;74(6):989-92. doi: 10.1016/j.mehy.2009.12.018. Epub 2010 Jan 27. Med Hypotheses. 2010. PMID: 20110149
-
[Frequency of delta F508 mutation in Venezuelan patients with cystic fibrosis].Invest Clin. 2004 Jun;45(2):121-30. Invest Clin. 2004. PMID: 15211979 Spanish.
-
Genetic and geographical variability in cystic fibrosis: evolutionary considerations.Ciba Found Symp. 1996;197:97-114; discussion 114-8. doi: 10.1002/9780470514887.ch6. Ciba Found Symp. 1996. PMID: 8827370 Review.
-
delta F508 in cystic fibrosis: willing but not able.Arch Dis Child. 1997 Mar;76(3):278-82. doi: 10.1136/adc.76.3.278. Arch Dis Child. 1997. PMID: 9135274 Free PMC article. Review. No abstract available.
Cited by
-
Mendelian inheritance revisited: dominance and recessiveness in medical genetics.Nat Rev Genet. 2023 Jul;24(7):442-463. doi: 10.1038/s41576-023-00574-0. Epub 2023 Feb 20. Nat Rev Genet. 2023. PMID: 36806206 Review.
-
Cystic fibrosis heterozygosity: Carrier state or haploinsufficiency?Proc Natl Acad Sci U S A. 2020 Feb 11;117(6):2740-2742. doi: 10.1073/pnas.1921730117. Epub 2020 Jan 28. Proc Natl Acad Sci U S A. 2020. PMID: 31992636 Free PMC article. No abstract available.
-
CFTR Heterozygotes Are at Increased Risk of Respiratory Infections: A Population-Based Study.Open Forum Infect Dis. 2018 Nov 1;5(11):ofy219. doi: 10.1093/ofid/ofy219. eCollection 2018 Nov. Open Forum Infect Dis. 2018. PMID: 30397620 Free PMC article.
-
Cystic fibrosis in Sudanese children: First report of 35 cases.Sudan J Paediatr. 2014;14(1):39-44. Sudan J Paediatr. 2014. PMID: 27493388 Free PMC article.
-
Heterozygosity for the F508del mutation in the cystic fibrosis transmembrane conductance regulator anion channel attenuates influenza severity.J Infect Dis. 2013 Sep 1;208(5):780-9. doi: 10.1093/infdis/jit251. Epub 2013 Jun 7. J Infect Dis. 2013. PMID: 23749967 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical