Literature DB >> 7687092

VNTR and microsatellite polymorphisms within the subtelomeric region of 7q.

A V Hing1, C Helms, H Donis-Keller.   

Abstract

The molecular basis of a highly polymorphic RFLP marker, HTY146c3 (D7S591), within the subtelomeric region of human chromosome 7q was determined by restriction-fragment and DNA sequence analysis. Two polymorphic systems were found--a simple base-substitution polymorphism and a GC-rich VNTR element with a core structure of C3AG2C2. In addition, a compound-imperfect CA dinucleotide-repeat element was identified approximately 10-20 kb from the telomeric sequence repeat (T2AG3), demonstrating that microsatellites can extend essentially to the ends of human chromosomes. The microsatellite marker, sAVH-6 (D7S594), is highly polymorphic, with 10 alleles and an observed heterozygosity of 84% found with the CEPH (Centre d'Etude du Polymorphisme Humain) reference pedigree collection. In combination with the RFLPs, the informativeness of the markers contained within 240 kb at the telomere approaches 100%. A unique genetic and physical STS marker, sAVH-6, defines the endpoint of the long arm of human chromosome 7.

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Year:  1993        PMID: 7687092      PMCID: PMC1682362     

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


  31 in total

1.  Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomal.

Authors:  H J Cooke; W R Brown; G A Rappold
Journal:  Nature       Date:  1985 Oct 24-30       Impact factor: 49.962

2.  Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q.

Authors:  M Litt; L B Jorde
Journal:  Am J Hum Genet       Date:  1986-08       Impact factor: 11.025

3.  Rapid detection and sequencing of alleles in the 3' flanking region of the interleukin-6 gene.

Authors:  A M Bowcock; A Ray; H Erlich; P B Sehgal
Journal:  Nucleic Acids Res       Date:  1989-09-12       Impact factor: 16.971

Review 4.  Hypervariable minisatellites: recombinators or innocent bystanders?

Authors:  A P Jarman; R A Wells
Journal:  Trends Genet       Date:  1989-11       Impact factor: 11.639

5.  High efficiency vectors for cosmid microcloning and genomic analysis.

Authors:  G A Evans; K Lewis; B E Rothenberg
Journal:  Gene       Date:  1989-06-30       Impact factor: 3.688

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.  A highly polymorphic region 3' to the human type II collagen gene.

Authors:  N G Stoker; K S Cheah; J R Griffin; F M Pope; E Solomon
Journal:  Nucleic Acids Res       Date:  1985-07-11       Impact factor: 16.971

8.  The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.

Authors:  G I Bell; M J Selby; W J Rutter
Journal:  Nature       Date:  1982-01-07       Impact factor: 49.962

9.  A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)n.

Authors:  A O Wilkie; J Lamb; P C Harris; R D Finney; D R Higgs
Journal:  Nature       Date:  1990-08-30       Impact factor: 49.962

10.  Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms.

Authors:  J L Weber
Journal:  Genomics       Date:  1990-08       Impact factor: 5.736

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  3 in total

1.  Characterization of short tandem repeats from thirty-one human telomeres.

Authors:  M Rosenberg; L Hui; J Ma; H C Nusbaum; K Clark; L Robinson; L Dziadzio; P M Swain; T Keith; T J Hudson; L G Biesecker; J Flint
Journal:  Genome Res       Date:  1997-09       Impact factor: 9.043

2.  A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.

Authors:  J L Blouin; D H Christie; A Gos; A Lynn; M A Morris; D H Ledbetter; A Chakravarti; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

3.  A novel acropectoral syndrome maps to chromosome 7q36.

Authors:  M Dundar; T M Gordon; I Ozyazgan; F Oguzkaya; Y Ozkul; A Cooke; A G Wilkinson; S Holloway; F R Goodman; J L Tolmie
Journal:  J Med Genet       Date:  2001-05       Impact factor: 6.318

  3 in total

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