Literature DB >> 7915880

Linkage disequilibrium in the insulin gene region: size variation at the 5' flanking polymorphism and bimodality among "class I" alleles.

R E McGinnis1, R S Spielman.   

Abstract

The 5' flanking polymorphism (5'FP), a hypervariable region at the 5' end of the insulin gene, has "class 1" alleles (650-900 bp long) that are in positive linkage disequilibrium with insulin-dependent diabetes mellitus (IDDM). We report that precise sizing of the 5'FP yields a bimodal frequency distribution of class 1 allele lengths. Class 1 alleles belonging to the lower component (650-750 bp) of the bimodal distribution were somewhat more highly associated with IDDM than were alleles from the upper component (760-900 bp), but the difference was not statistically significant. We also examined 5'FP length variation in relation to allelic variation at nearby polymorphisms. At biallelic RFLPs on both sides of the 5'FP, we found that one allele exhibits near-total association with the upper component of the 5'FP class 1 distribution. Such associations represent a little-known but potentially widespread form of linkage disequilibrium. In this type of disequilibrium, a flanking allele has near-complete association with a single mode of VNTR alleles whose lengths represent consecutive numbers of tandem repeats (CNTR). Such extreme disequilibrium between a CNTR mode and flanking alleles may originate and persist because length mutations at some VNTR loci usually add or delete only one or two repeat units.

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Year:  1994        PMID: 7915880      PMCID: PMC1918400     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  21 in total

1.  Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations.

Authors:  R Deka; R Chakraborty; S DeCroo; F Rothhammer; S A Barton; R E Ferrell
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

2.  The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models.

Authors:  R C Lewontin
Journal:  Genetics       Date:  1964-01       Impact factor: 4.562

3.  Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination.

Authors:  C Oudet; R Heilig; A Hanauer; J L Mandel
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

4.  Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.

Authors:  N J Cox; G I Bell; K S Xiang
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

5.  Evidence for increased recombination near the human insulin gene: implication for disease association studies.

Authors:  A Chakravarti; S C Elbein; M A Permutt
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

6.  HLA-DR effects in a large German IDDM dataset.

Authors:  L L Field; C Fothergill-Payne; J Bertrams; M P Baur
Journal:  Genet Epidemiol Suppl       Date:  1986

7.  Analysis of endonuclease R-EcoRI fragments of DNA from lambdoid bacteriophages and other viruses by agarose-gel electrophoresis.

Authors:  R B Helling; H M Goodman; H W Boyer
Journal:  J Virol       Date:  1974-11       Impact factor: 5.103

8.  Mutation of human short tandem repeats.

Authors:  J L Weber; C Wong
Journal:  Hum Mol Genet       Date:  1993-08       Impact factor: 6.150

9.  The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.

Authors:  G I Bell; M J Selby; W J Rutter
Journal:  Nature       Date:  1982-01-07       Impact factor: 49.962

10.  Human tyrosine hydroxylase and insulin genes are contiguous on chromosome 11.

Authors:  K L O'Malley; P Rotwein
Journal:  Nucleic Acids Res       Date:  1988-05-25       Impact factor: 16.971

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  4 in total

1.  Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.

Authors:  X Liu; D F Barker
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

2.  HLA DQA1-DQB1-TAP2 haplotypes in IDDM families: no evidence for an additional contribution to disease risk by the TAP2 locus.

Authors:  L Esposito; V Lampasona; E Bosi; F Poli; M Ferrari; E Bonifacio
Journal:  Diabetologia       Date:  1995-08       Impact factor: 10.122

3.  Diabetes susceptibility at IDDM2 cannot be positively mapped to the VNTR locus of the insulin gene.

Authors:  A Doria; J Lee; J H Warram; A S Krolewski
Journal:  Diabetologia       Date:  1996-05       Impact factor: 10.122

4.  Polymorphism in regulatory gene sequences.

Authors:  N A Mitchison
Journal:  Genome Biol       Date:  2000-12-20       Impact factor: 13.583

  4 in total

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