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PMID: 9150719 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival.

Human genetics ·Vol. 99 ·No. 5 ·1997-05-00 ·Pages 565-72

Macek M, Macek M, Krebsová A, Nash E, Hamosh A, Reis A, Varon-Mateeva R, Schmidtke J, Maestri NE, Sperling K, Krawczak M, Cutting GR

Abstract

Cystic fibrosis (CF) patients show a high degree of linkage disequilibrium between the CF transmembrane conductance regulator (CFTR) gene and polymorphisms 5' of that gene. To determine whether the region 5' of CFTR contains biologically important sequences, the allele frequencies of six CFTR-linked polymorphisms (metH/MspI, XV-2c/TaqI, CS.7/HhaI, KM19/PstI, MP6d9/MspI, J44/XbaI) were determined in 417 randomly selected elderly individuals (over 75 years of age) from the Czech population. The elderly individuals were considered "escapees" of strong selective pressures that had operated during their lifetime, prior to the introduction of modern health care since 1950. The pooled allele frequencies of the analyzed marker polymorphisms in the elderly did not significantly differ from published data. However, when analyzed by ex, the allele frequencies of markers CS.7/HhaI and KM19/PstI differed significantly (P < 0.05) between elderly females and males. The allele frequencies of the six polymorphisms were then determined in 646 newborns and 345 young adults of reproductive age; these individuals were selected in a similar manner and drawn from the same population. In these control groups, the studied marker polymorphisms exhibited no statistically significant differences between sexes and/or between individuals of the same sex, only between different age groups. A gradual relative increase in the frequency of allele "2" of marker CS.7/HhaI was observed from newborn females to elderly women, the overall difference in allele frequencies of this marker polymorphism between newborn females and elderly women reaching statistical significance (P < 0.05). Interestingly, allele "2" is the major constituent of the extended "B-haplotype", which is in strong linkage disequilibrium with common CF alleles. Taken together, our data suggest that the region spanning markers CS.7 and KM19 is associated with a genetic factor that influences postnatal female survival, providing a possible mechanism for increasing the frequency of particular mutations in the adjacent CFTR gene.

MeSH Terms
Adult Age Factors Aged Cystic Fibrosis/genetics,mortality Cystic Fibrosis Transmembrane Conductance Regulator/genetics Female Gene Frequency Genetic Linkage Humans Infant, Newborn Male Point Mutation Polymorphism, Genetic Restriction Mapping Survival Rate
Chemicals
CFTR protein, human Cystic Fibrosis Transmembrane Conductance Regulator
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Macek M
Center for Medical Genetics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Macek M
Krebsová A
Nash E
Hamosh A
Reis A
Varon-Mateeva R
Schmidtke J
Maestri N E
Sperling K
Krawczak M
Cutting G R
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1997-05-00
Pages
565-72
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
Grants
NIDDK NIH HHS · DK 44003 · United States
NIDDK NIH HHS · K08 DK0215 · United States
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