Literature DB >> 2002494

An analysis of amplified insulin gene products in diabetics of Indian origin.

G A Hitman1, P K Kambo, M Viswanathan, V Mohan.   

Abstract

We have previously described an increased incidence of the class 3 allele of the hypervariable region (HVR) 5' to the insulin gene in south Indian non-insulin dependent diabetics; this association is absent in Punjabi Sikhs with this disorder. Using the polymerase chain reaction we have amplified parts of the insulin gene from 130 subjects to look for mutations which may be in linkage disequilibrium with the class 3 allele and hence explain its association with non-insulin dependent diabetes (NIDDM). In 23 south Indian subjects with NIDDM, using the restriction enzyme MboII, a B chain mutant (insulin Chicago) was excluded. Two patterns (alpha and beta) were found, representing a PstI polymorphism in the 3' untranslated region of the insulin gene. In subjects homozygous for the class 1 allele, the allelic frequency for alpha was 0.94 (143/152) and for beta was 0.06, in heterozygotes (1,3) alpha 0.63 (54/86) and beta 0.37, and in homozygotes for the class 3 allele alpha 0.18 (4/22) and beta 0.82 (p less than 0.001), thus establishing linkage disequilibrium between these two loci. No differences in allelic frequency were found in the south Indians or Punjabi Sikhs between controls and the different types of non-insulin requiring diabetes (NIDDM, fibrocalculous pancreatic diabetes and maturity onset diabetes of the young) when both groups were matched for insulin genotypes. Thus, although this polymorphism in the 3' untranslated region of the insulin gene is in linkage disequilibrium with the class 3 allele, it does not appear to be any better at predicting diabetes than the class 3 allele itself.

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Year:  1991        PMID: 2002494      PMCID: PMC1016776          DOI: 10.1136/jmg.28.2.97

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  26 in total

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2.  Evolution of the hemoglobin S and C genes in world populations.

Authors:  Y W Kan; A M Dozy
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Authors:  G A Hitman; N I Jowett; L G Williams; S Humphries; R M Winter; D J Galton
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4.  Restriction fragment length polymorphism of the insulin gene in diabetes mellitus.

Authors:  D Owerbach; J Nerup
Journal:  Diabetes       Date:  1982-03       Impact factor: 9.461

5.  Spontaneous remission of multi-system histiocytosis X.

Authors:  V Broadbent; J Pritchard; E G Davies; R J Levinsky; D Heaf; D J Atherton; J R Pincott; S Tucker
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6.  Diabetic hypertriglyceridaemia and related 5' flanking polymorphism of the human insulin gene.

Authors:  N I Jowett; L G Williams; G A Hitman; D J Galton
Journal:  Br Med J (Clin Res Ed)       Date:  1984-01-14

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Authors:  G I Bell; S Horita; J H Karam
Journal:  Diabetes       Date:  1984-02       Impact factor: 9.461

8.  Genetic variation in the human insulin gene.

Authors:  A Ullrich; T J Dull; A Gray; J Brosius; I Sures
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9.  Identification of a point mutation in the human insulin gene giving rise to a structurally abnormal insulin (insulin Chicago).

Authors:  S C Kwok; D F Steiner; A H Rubenstein; H S Tager
Journal:  Diabetes       Date:  1983-09       Impact factor: 9.461

10.  HLA and non-insulin dependent diabetes in Fiji indians.

Authors:  S W Serjeantson; D P Ryan; P Ram; P Zimmet
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  4 in total

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Authors:  W Horst-Sikorska; B Zoll; J Kwiatkowska; B Willms; A Kraszewski; A Horst; R Slomski
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3.  Allelic divergence in the human insulin gene provides evidence for intragenic recombination events in the non-coding regions: evidence for existence of new alleles.

Authors:  Y S Kim; M H Kim; Y K Choi; C H Kim; D S Lee
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4.  Genetic variation of the transcription factor GATA3, not STAT4, is associated with the risk of type 2 diabetes in the Bangladeshi population.

Authors:  Nafiul Huda; Md Ismail Hosen; Tahirah Yasmin; Pankaj Kumar Sarkar; A K M Mahbub Hasan; A H M Nurun Nabi
Journal:  PLoS One       Date:  2018-07-25       Impact factor: 3.240

  4 in total

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