Literature DB >> 2901393

TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia.

K Yamakawa1, T Okafuji, Y Iwamura, K Yuzawa, J Satoh, N Hattori, Y Yamanouchi, H Yanagi, K Kawai, S Tsuchiya.   

Abstract

The low density lipoprotein (LDL) receptor gene was analyzed in 67 unrelated healthy Japanese and 38 members of six consecutive families with familial hypercholesterolemia (FH) by Southern blot hybridization with TaqI, an LDL receptor cDNA fragment containing exons 1 to 8 being used as a probe. A new TaqI RFLP at the LDL receptor locus was detected with allele frequencies of 0.67 and 0.33. The data obtained with smaller cDNA subfragment probes revealed that the TaqI RFLP site is located within 1.1 kb of the 5' side of the EcoRI site of exon 5. The TaqI RFLP was in linkage disequilibrium with the PstI RFLP but showed no significant linkage disequilibrium with the RFLPs for AvaII, ApaLI/I15, PvuII, NcoI, and ApaLI/3'. Among the seven RFLPs at the LDL receptor locus, the TaqI RFLP was the only useful genetic marker in one of the six families with FH. Furthermore, the association of an additional TaqI 1.5-kb band with a mutant LDL receptor gene was observed in another family with FH in which the proband was homozygous for all of the seven RFLPs. The data obtained with various restriction enzymes and smaller cDNA subfragments probes suggested that a minor change in nucleotide sequences in the region including exons 5 to 8 is present in the mutant gene. These data suggest that the TaqI RFLP is a useful genetic marker at the LDL receptor locus and that TaqI serves for the analysis of some mutant LDL receptor genes, when used with small LDL receptor cDNA probes.

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Year:  1988        PMID: 2901393     DOI: 10.1007/bf00451446

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


  23 in total

1.  Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots.

Authors:  H Youssoufian; H H Kazazian; D G Phillips; S Aronis; G Tsiftis; V A Brown; S E Antonarakis
Journal:  Nature       Date:  1986 Nov 27-Dec 3       Impact factor: 49.962

2.  Double Msp I RFLP in the human LDL receptor gene.

Authors:  J Geisel; B Weisshaar; K Oette; M Mechtel; W Doerfler
Journal:  Nucleic Acids Res       Date:  1987-05-11       Impact factor: 16.971

3.  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

4.  Human LDL receptor gene: two ApaLI RFLPs.

Authors:  E Leitersdorf; H H Hobbs
Journal:  Nucleic Acids Res       Date:  1987-03-25       Impact factor: 16.971

5.  AvaII polymorphism in the human LDL receptor gene.

Authors:  H H Hobbs; V Esser; D W Russell
Journal:  Nucleic Acids Res       Date:  1987-01-12       Impact factor: 16.971

6.  Strategies for detecting and characterizing restriction fragment length polymorphisms (RFLP's).

Authors:  M H Skolnick; R White
Journal:  Cytogenet Cell Genet       Date:  1982

7.  RFLP for the human LDL receptor gene (LDLR): Bst EII.

Authors:  L T Steyn; A Pretorius; P A Brink; A J Bester
Journal:  Nucleic Acids Res       Date:  1987-06-11       Impact factor: 16.971

8.  A RFLP associated with the low-density lipoprotein receptor gene (LDLR).

Authors:  M J Kotze; E Langenhoven; E Dietzsch; A E Retief
Journal:  Nucleic Acids Res       Date:  1987-01-12       Impact factor: 16.971

Review 9.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

10.  Identification of deletions in the human low density lipoprotein receptor gene.

Authors:  B Horsthemke; A Dunning; S Humphries
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

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  6 in total

1.  Family studies of the LDL receptor gene of relatively severe hereditary hypercholesterolemia associated with Achilles tendon xanthomas.

Authors:  K Yamakawa; H Yanagi; K Saku; J Sasaki; T Okafuji; Y Shimakura; K Kawai; S Tsuchiya; K Takada; S Naito
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

2.  Three novel partial deletions of the low-density lipoprotein (LDL) receptor gene in familial hypercholesterolemia.

Authors:  K Yamakawa; K Takada; H Yanagi; S Tsuchiya; K Kawai; S Nakagawa; G Kajiyama; H Hamaguchi
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

3.  Identification of the serine-156 to leucine mutation in the low-density lipoprotein receptor in a German family with familial hypercholesterolemia.

Authors:  H Schuster; P Ostwald; P Keller; G Wolfram; C Keller
Journal:  Clin Investig       Date:  1993-02

4.  Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemia.

Authors:  H Schuster; H J Fischer; C Keller; G Wolfram; N Zöllner
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

5.  Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene.

Authors:  T Matsunaga; Y Hiasa; H Yanagi; T Maeda; N Hattori; K Yamakawa; Y Yamanouchi; I Tanaka; T Obara; H Hamaguchi
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-01       Impact factor: 11.205

6.  South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch population.

Authors:  J C Defesche; D E van Diermen; P J Lansberg; R J Lamping; P W Reymer; M R Hayden; J J Kastelein
Journal:  Hum Genet       Date:  1993-12       Impact factor: 4.132

  6 in total

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