Literature DB >> 8116620

Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes.

R Decorte1, R Wu, P Marynen, J J Cassiman.   

Abstract

The PCR technique was used to analyze the DXYS17 locus in the pseudoautosomal region of the X and the Y chromosomes. Analysis on an automated DNA sequencer allowed for sensitive and highly accurate typing of 16 different alleles with a size between 480 and 1,100 bp. Two DXYS17 alleles migrated with the same size on agarose or denaturing polyacrylamide gels but with different mobilities on nondenaturing polyacrylamide gels. Sequence analysis showed that, while an identical number of repeats were present in both alleles, differences in the composition of the units were observed. The origin of these differences was found in the 28- and 33-bp units, which only had a specific repeat pattern at the 5' and 3' ends of the region. The genotype distribution for DXYS17 in a Caucasian population did not deviate from the values expected under Hardy-Weinberg equilibrium. However, the frequency of one allele and one genotype was significantly different between males and females. Segregation analysis showed that this difference was the result of a nonrandom distribution of certain alleles on the sex chromosomes in males.

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Year:  1994        PMID: 8116620      PMCID: PMC1918131     

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


  25 in total

1.  Rapid detection of hypervariable regions by the polymerase chain reaction technique.

Authors:  R Decorte; H Cuppens; P Marynen; J J Cassiman
Journal:  DNA Cell Biol       Date:  1990 Jul-Aug       Impact factor: 3.311

2.  Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE.

Authors:  B Budowle; R Chakraborty; A M Giusti; A J Eisenberg; R C Allen
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

3.  Estimation of average heterozygosity and genetic distance from a small number of individuals.

Authors:  M Nei
Journal:  Genetics       Date:  1978-07       Impact factor: 4.562

4.  Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes.

Authors:  M C Simmler; F Rouyer; G Vergnaud; M Nyström-Lahti; K Y Ngo; A de la Chapelle; J Weissenbach
Journal:  Nature       Date:  1985 Oct 24-30       Impact factor: 49.962

5.  A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes.

Authors:  F Rouyer; M C Simmler; C Johnsson; G Vergnaud; H J Cooke; J Weissenbach
Journal:  Nature       Date:  1986 Jan 23-29       Impact factor: 49.962

6.  Characterization of the COL2A1 VNTR polymorphism.

Authors:  E S Berg; B Olaisen
Journal:  Genomics       Date:  1993-05       Impact factor: 5.736

7.  Anomalous electrophoresis of deoxyribonucleic acid restriction fragments on polyacrylamide gels.

Authors:  N C Stellwagen
Journal:  Biochemistry       Date:  1983-12-20       Impact factor: 3.162

8.  Population amalgamation and genetic variation: observations on artificially agglomerated tribal populations of Central and South America.

Authors:  R Chakraborty; P E Smouse; J V Neel
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

9.  Direct electrophoretic detection of the allelic state of single DNA molecules in human sperm by using the polymerase chain reaction.

Authors:  H Li; X Cui; N Arnheim
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

10.  Two highly polymorphic minisatellites from the pseudoautosomal region of the human sex chromosomes.

Authors:  M C Simmler; C Johnsson; C Petit; F Rouyer; G Vergnaud; J Weissenbach
Journal:  EMBO J       Date:  1987-04       Impact factor: 11.598

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  3 in total

1.  Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.

Authors:  R M Chalmers; M B Davis; M G Sweeney; N W Wood; A E Harding
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

2.  Inference of population subdivision from the VNTR distributions of New Zealanders.

Authors:  A G Clark; J F Hamilton; G K Chambers
Journal:  Genetica       Date:  1995       Impact factor: 1.082

3.  Mechanisms underlying telomere repeat turnover, revealed by hypervariable variant repeat distribution patterns in the human Xp/Yp telomere.

Authors:  D M Baird; A J Jeffreys; N J Royle
Journal:  EMBO J       Date:  1995-11-01       Impact factor: 11.598

  3 in total

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