Literature DB >> 8502559

Variant mapping of the Apo(B) AT rich minisatellite. Dependence on nucleotide sequence of the copy number variations. Instability of the non-canonical alleles.

E Desmarais1, S Vigneron, C Buresi, F Cambien, J P Cambou, G Roizes.   

Abstract

Because of its variations in length, the AT rich Hyper-Variable Region (HVR) of the 3' end of the Apolipoprotein B gene is used as a polymorphic maker in genetic studies. It contains a SspI site in its repeated motif and we used this feature to precisely analyse the internal structure of the different alleles found at this locus in a Caucasian population. We performed total digestion on 194 alleles as well as Minisatellite Variant Repeat mapping (MVR mapping: partial digestion) on 54. The results show that the level of length variability (in copy number) of the 5' end of this locus is at least two times higher than that of the 3' end. This could be correlated with the difference in nucleotide sequence between the two parts of the HVR and suggests the dependence on the primary structure of the mechanism that produces length variability. A molecular model is proposed to explain this result. Moreover, the sharp analysis of the minisatellite structure by the distribution of SspI sites reveals differences between long and short alleles, indicating that in most cases, no recombination occurs between alleles of different sizes. Finally the rare alleles exhibit a non-canonical structure. These important points could explain the bimodal distribution of the frequencies of the alleles in the population.

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Year:  1993        PMID: 8502559      PMCID: PMC309482          DOI: 10.1093/nar/21.9.2179

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  28 in total

1.  Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

Authors:  A J Jeffreys; N J Royle; V Wilson; Z Wong
Journal:  Nature       Date:  1988-03-17       Impact factor: 49.962

2.  Variable number of tandem repeat (VNTR) markers for human gene mapping.

Authors:  Y Nakamura; M Leppert; P O'Connell; R Wolff; T Holm; M Culver; C Martin; E Fujimoto; M Hoff; E Kumlin
Journal:  Science       Date:  1987-03-27       Impact factor: 47.728

3.  Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region.

Authors:  E Boerwinkle; W J Xiong; E Fourest; L Chan
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

4.  The polymorphism ApoB/4311 in patients with myocardial infarction and controls: the ECTIM Study.

Authors:  J F Moreel; G Roizes; A E Evans; D Arveiler; J P Cambou; C Souriau; H J Parra; E Desmarais; J C Fruchart; P Ducimetière
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

5.  A hypervariable region 3' to the human apolipoprotein B gene.

Authors:  T J Knott; S C Wallis; R J Pease; L M Powell; J Scott
Journal:  Nucleic Acids Res       Date:  1986-11-25       Impact factor: 16.971

6.  Hypervariable 'minisatellite' regions in human DNA.

Authors:  A J Jeffreys; V Wilson; S L Thein
Journal:  Nature       Date:  1985 Mar 7-13       Impact factor: 49.962

7.  The evolution of restricted recombination and the accumulation of repeated DNA sequences.

Authors:  B Charlesworth; C H Langley; W Stephan
Journal:  Genetics       Date:  1986-04       Impact factor: 4.562

8.  A highly polymorphic locus in human DNA.

Authors:  A R Wyman; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

9.  Human population genetic studies of five hypervariable DNA loci.

Authors:  I Balazs; M Baird; M Clyne; E Meade
Journal:  Am J Hum Genet       Date:  1989-02       Impact factor: 11.025

10.  A unique AT-rich hypervariable minisatellite 3' to the ApoB gene defines a high information restriction fragment length polymorphism.

Authors:  L S Huang; J L Breslow
Journal:  J Biol Chem       Date:  1987-07-05       Impact factor: 5.157

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  4 in total

1.  Evolutionary fate of an unstable human minisatellite deduced from sperm-mutation spectra of individual alleles.

Authors:  Jérôme Buard; Charles Brenner; Alec J Jeffreys
Journal:  Am J Hum Genet       Date:  2002-02-21       Impact factor: 11.025

2.  Germline mosaicism for an alanine to valine substitution at residue beta 140 in hemoglobin Puttelange, a new variant with high oxygen affinity.

Authors:  H Wajcman; E Girodon; D Promé; M L North; F Plassa; I Duwig; J Kister; J P Bergerat; F Oberling; E Lampert
Journal:  Hum Genet       Date:  1995-12       Impact factor: 4.132

3.  VNTR alleles associated with the alpha-globin locus are haplotype and population related.

Authors:  J J Martinson; A J Boyce; J B Clegg
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025

4.  Diversity of ethnic and racial VNTR RFLP fixed-bin frequency distributions.

Authors:  J Hartmann; R Keister; B Houlihan; L Thompson; R Baldwin; E Buse; B Driver; M Kuo
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

  4 in total

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