Literature DB >> 3855405

Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19.

J A Donald, S C Wallis, A Kessling, P Tippett, E B Robson, S Ball, K E Davies, P Scambler, K Berg, A Heiberg.   

Abstract

Two common restriction fragment length polymorphisms detected with cloned gene probes for apolipoprotein CII (apo CII) have been used to study the inheritance of the gene in families segregating for loci on chromosome 19. Lod scores for APOC2 with the gene for complement component 3 (C3) exclude close linkage and give a maximum at a male recombination fraction of 0.25-0.30. Lod scores for APOC2 and FHC, the gene causing familial hypercholesterolaemia, are negative in males and suggest the genes may not be linked. However, it appears that APOC2 may be closely linked to the blood group loci Lutheran (Lu) and Secretor (Se), and probably less closely linked to Lewis (Le). These data are consistent with the gene order: FHC-----C3-----(Lu, Se, APOC2)

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Year:  1985        PMID: 3855405     DOI: 10.1007/bf00295527

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  34 in total

1.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

2.  Characterization and quantitation of the apolipoproteins from human chyle chylomicrons.

Authors:  G Kostner; A Holasek
Journal:  Biochemistry       Date:  1972-03-28       Impact factor: 3.162

3.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

4.  Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.

Authors:  J H Renwick; S E Bundey; M A Ferguson-Smith; M M Izatt
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

5.  A specific apoprotein activator for lipoprotein lipase.

Authors:  J C LaRosa; R I Levy; P Herbert; S E Lux; D S Fredrickson
Journal:  Biochem Biophys Res Commun       Date:  1970-10-09       Impact factor: 3.575

6.  Linkage between familial hypercholesterolemia with xanthomatosis and the C3 polymorphism confirmed.

Authors:  K Berg; A Heiberg
Journal:  Cytogenet Cell Genet       Date:  1978

7.  Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.

Authors:  C L Jackson; G A Bruns; J L Breslow
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

8.  Primary structure of very low density apolipoprotein C-II of human plasma.

Authors:  R L Jackson; H N Baker; E B Gilliam; A M Gotto
Journal:  Proc Natl Acad Sci U S A       Date:  1977-05       Impact factor: 11.205

9.  The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man.

Authors:  B Olaisen; P Teisberg; T Gedde-Dahl
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

10.  Hypertriglyceridemia associated with deficiency of apolipoprotein C-II.

Authors:  W C Breckenridge; J A Little; G Steiner; A Chow; M Poapst
Journal:  N Engl J Med       Date:  1978-06-08       Impact factor: 91.245

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  12 in total

1.  Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.

Authors:  D J Shaw; A L Meredith; M Sarfarazi; H G Harley; S M Huson; J D Brook; L Bufton; M Litt; T Mohandas; P S Harper
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

2.  Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19.

Authors:  F Tata; I Henry; A F Markham; S C Wallis; D Weil; K H Grzeschik; C Junien; R Williamson; S E Humphries
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 3.  Diagnosis of genetic disease using recombinant DNA.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

4.  Human genes involved in cholesterol metabolism: chromosomal mapping of the loci for the low density lipoprotein receptor and 3-hydroxy-3-methylglutaryl-coenzyme A reductase with cDNA probes.

Authors:  V Lindgren; K L Luskey; D W Russell; U Francke
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

5.  A common restriction fragment length polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidaemia.

Authors:  E C Klasen; P J Talmud; L Havekes; E de Wit; E van der Kooij-Meijs; M Smit; G Hansson; S E Humphries
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

6.  The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene.

Authors:  S C Wallis; J A Donald; L A Forrest; R Williamson; S E Humphries
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair.

Authors:  R L Stallings; E Olson; A W Strauss; L H Thompson; L L Bachinski; M J Siciliano
Journal:  Am J Hum Genet       Date:  1988-08       Impact factor: 11.025

8.  The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase).

Authors:  S E Humphries; F Tata; I Henry; F Barichard; M Holm; C Junien; R Williamson
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

9.  Localization of genes encoding apolipoproteins CI, CII, and E to the p13----cen region of human chromosome 19.

Authors:  J Scott; T J Knott; D J Shaw; J D Brook
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemia.

Authors:  M Smit; E van der Kooij-Meijs; R R Frants; L Havekes; E C Klasen
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

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