Literature DB >> 8471544

Genetic variation of microsatellite markers D1S117, D6S89, D11S35, APOC2, and D21S168 in the Spanish population.

J J Fuentes1, I Banchs, V Volpini, X Estivill.   

Abstract

We have used PCR amplification to analyse the allele frequency, distribution and heterozygosity of 5 microsatellite markers (D1S117, D6S89, D11S35, APOC2, and D21S168), in a sample of 100 unrelated Spanish individuals. The loci tested exhibit wide allelic variability having 7-17 alleles, PIC (polymorphic information content) between 0.79 and 0.86, and heterozygosity between 0.81 and 0.86. D1S117 and D21S168 have unimodal distribution, APOC2 has 4 common alleles which account for 71% of the total variation, D11S35 has a bimodal distribution and D6S89 is trimodal. The allelic distribution observed for each locus is in agreement with slippage and mispairing as the main mechanisms involved in the evolution of microsatellite alleles. Multiplex amplification of loci D6S89 and APOC2 was possible due to their non-overlapping allele sizes. The rapidity with which microsatellites can be analysed, and the accurate determination of alleles, make these markers very powerful tools for genetic typing. The information obtained for loci D1S117, D6S89, D11S35, APOC2, and D21S168, provides a basis for their use for DNA typing and paternity analysis in the Spanish population.

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Year:  1993        PMID: 8471544     DOI: 10.1007/bf01370384

Source DB:  PubMed          Journal:  Int J Legal Med        ISSN: 0937-9827            Impact factor:   2.686


  34 in total

1.  Dinucleotide repeat polymorphism at the D11S35 locus.

Authors:  M Litt; V Sharma; J A Luty
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

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Authors:  B Devlin; N Risch; K Roeder
Journal:  Science       Date:  1990-09-21       Impact factor: 47.728

3.  Dinucleotide repeat polymorphism at the D1S117 locus.

Authors:  V Sharma; M Litt
Journal:  Nucleic Acids Res       Date:  1991-03-11       Impact factor: 16.971

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Authors:  A Edwards; H A Hammond; L Jin; C T Caskey; R Chakraborty
Journal:  Genomics       Date:  1992-02       Impact factor: 5.736

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Journal:  Nature       Date:  1985 Mar 7-13       Impact factor: 49.962

6.  Parental origin of mutations of the retinoblastoma gene.

Authors:  T P Dryja; S Mukai; R Petersen; J M Rapaport; D Walton; D W Yandell
Journal:  Nature       Date:  1989-06-15       Impact factor: 49.962

7.  CA/GT microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingover.

Authors:  N Morral; V Nunes; T Casals; X Estivill
Journal:  Genomics       Date:  1991-07       Impact factor: 5.736

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

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Authors:  N Morral; X Estivill
Journal:  Genomics       Date:  1992-08       Impact factor: 5.736

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Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

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  3 in total

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Authors:  A Sánchez; M Milà; S Castellví-Bel; M Rosich; D Jiménez; C Badenas; X Estivill
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-05       Impact factor: 10.154

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Authors:  H Kruyer; M Milà; G Glover; P Carbonell; F Ballesta; X Estivill
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

3.  De novo missense mutation Y174S in exon 1 of the adrenoleukodystrophy (ALD) gene.

Authors:  A Barceló; M Girós; C O Sarde; G Pintos; J L Mandel; T Pàmpols; X Estivill
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132

  3 in total

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