Home LiteratureArticle Details
PMID: 2897786 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study.

American journal of human genetics ·Vol. 43 ·No. 1 ·1988-07-00 ·Pages 23-8

Estivill X, Farrall M, Williamson R, Ferrari M, Seia M, Giunta AM, Novelli G, Potenza L, Dallapicolla B, Borgo G

Abstract

The locus D7S23 includes a CpG-enriched methylation-free island that maps midway between the markers J3.11 and met and is genetically very close to the mutation causing cystic fibrosis (CF). We have studied the linkage disequilibrium between four polymorphic markers from this locus (KM.19, CS.7, XV-2c, and PT-3) and the CF mutation (CF) in 127 Italian families. Strong linkage disequilibrium is found between KM.19, CS.7, and CF, and weaker but significant disequilibrium is found between XV-2c, PT-3, and CF. The disequilibrium between markers and CF for the Italian population provides additional information on the origin and homogeneity of the CF defect. This panel of probes is sufficiently informative to permit accurate prenatal diagnosis of CF in most families with an affected person, and the disequilibrium also allows indirect carrier detection/exclusion in some cases.

MeSH Terms
Alleles Cystic Fibrosis/genetics DNA/genetics Genetic Carrier Screening Genetic Linkage Genetic Markers Humans Polymorphism, Genetic Polymorphism, Restriction Fragment Length
Chemicals
Genetic Markers DNA
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Estivill X
Department of Biochemistry and Molecular Genetics, St. Mary's Hospital Medical School, London, United Kingdom.
Farrall M
Williamson R
Ferrari M
Seia M
Giunta A M
Novelli G
Potenza L
Dallapicolla B
Borgo G
References (9)
9 references, click to expand
  1. "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.
    Anal Biochem. 1984 Feb;137(1):266-7 PMID: 6329026
  2. A closely linked genetic marker for cystic fibrosis.
    Nature. 1985 Nov 28-Dec 4;318(6044):382-4 PMID: 3906407
  3. Localization of cystic fibrosis locus to human chromosome 7cen-q22.
    Nature. 1985 Nov 28-Dec 4;318(6044):384-5 PMID: 2999612
  4. Isolation of a further anonymous informative DNA sequence from chromosome seven closely linked to cystic fibrosis.
    Nucleic Acids Res. 1986 Mar 11;14(5):1951-6 PMID: 3960715
  5. Patterns of polymorphism and linkage disequilibrium for cystic fibrosis.
    Genomics. 1987 Nov;1(3):257-63 PMID: 2895728
  6. Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.
    Hum Genet. 1987 May;76(1):40-6 PMID: 2883110
  7. A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands.
    Nature. 1987 Apr 30-May 6;326(6116):840-5 PMID: 2883581
  8. Indirect cystic fibrosis carrier detection.
    Lancet. 1987 Jul 18;2(8551):156-7 PMID: 2885615
  9. CpG-rich islands and the function of DNA methylation.
    Nature. 1986 May 15-21;321(6067):209-13 PMID: 2423876
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1988-07-00
Pages
23-8
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1715296
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com