Literature DB >> 3243549

Molecular characterization of a spontaneously generated new allele at a VNTR locus: no exchange of flanking DNA sequence.

R K Wolff1, Y Nakamura, R White.   

Abstract

Variable-number tandem-repeat (VNTR) DNA markers are contributing new power to human genetic studies because their hypervariable nature allows individualization at the DNA level. The practical value of VNTR markers has been well established for genetic linkage mapping, forensic biology, paternity testing, and monitoring of bone marrow transplants. A popular hypothesis attributes generation of variability at VNTR loci to unequal exchange between homologous chromosomes at meiosis. Contrary to the prediction of this hypothesis, we report here the finding that a newly generated VNTR allele is parental for closely spaced flanking markers; the new allele was generated by loss of one repeat unit, without exchange of flanking DNA sequences. These results are consistent with sister chromatid exchange and polymerase slippage or deletion, as well as with some models for gene conversion.

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Year:  1988        PMID: 3243549     DOI: 10.1016/0888-7543(88)90126-7

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  45 in total

1.  Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90).

Authors:  J Buard; A C Shone; A J Jeffreys
Journal:  Am J Hum Genet       Date:  2000-06-26       Impact factor: 11.025

2.  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

3.  Population genetics and forensic efficiency data of 4 AMPFLP's.

Authors:  S Rand; C Puers; K Skowasch; P Wiegand; B Budowle; B Brinkmann
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

4.  Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations.

Authors:  R Deka; S De Croo; L M Yu; R E Ferrell
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

5.  The evolution of tandemly repetitive DNA: recombination rules.

Authors:  R M Harding; A J Boyce; J B Clegg
Journal:  Genetics       Date:  1992-11       Impact factor: 4.562

6.  DNA extraction from mixtures of body fluid using mild preferential lysis.

Authors:  P Wiegand; M Schürenkamp; U Schütte
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

7.  Bloom's syndrome. XVIII. Hypermutability at a tandem-repeat locus.

Authors:  J Groden; J German
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

8.  Characterization of a low copy repetitive element S232 involved in the generation of frequent deletions of the distal short arm of the human X chromosome.

Authors:  X M Li; P H Yen; L J Shapiro
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

9.  Minisatellite allele diversification: the origin of rare alleles at the HRAS1 locus.

Authors:  A Kasperczyk; N A DiMartino; T G Krontiris
Journal:  Am J Hum Genet       Date:  1990-11       Impact factor: 11.025

10.  Recurrent 3-bp deletion at codon 255/256 of the rhodopsin gene in a German pedigree with autosomal dominant retinitis pigmentosa.

Authors:  A Artlich; M Horn; B Lorenz; S Bhattacharga; A Gal
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

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