Literature DB >> 8314574

Characterization of the COL2A1 VNTR polymorphism.

E S Berg1, B Olaisen.   

Abstract

The variable number of tandem repeat (VNTR) region 3' to the collagen type II gene (COL2A1) was amplified in vitro by the polymerase chain reaction. Subsequent high-resolution gel electrophoresis showed that the five earlier reported alleles could be further subtyped. A total of 17 allelic variants with a heterozygosity of 73.0% were found in 202 unrelated Norwegians. DNA sequencing of 19 COL2A1 alleles has been performed. The internal organization of the VNTR was common for all alleles, as previously shown for a few alleles. Moreover, the polymorphism in the COL2A1 locus is mainly due to variation in the numbers of copies of two repeat units, containing 34 and 31 bp, respectively, and/or to small deletions in either of the two units. DNA sequencing of alleles with the same electrophoretic size revealed no heterogeneity such as an alternating order of the different units, a feature that might have been expected to be the result of unequal crossing-over events. The observed ordered structure of the VNTR and the possibility of single-stranded DNA from the cores in the VNTR forming hairpins and loops suggest that the COL2A1 polymorphism may have evolved mainly by replication slippage mechanisms.

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Year:  1993        PMID: 8314574     DOI: 10.1006/geno.1993.1196

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


  8 in total

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Authors:  R Decorte; R Wu; P Marynen; J J Cassiman
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2.  Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritance.

Authors:  L D Spotila; J Caminis; M Devoto; K Shimoya; L Sereda; J Ott; M P Whyte; A Tenenhouse; D J Prockop
Journal:  Mol Med       Date:  1996-05       Impact factor: 6.354

3.  Genetic linkage analysis of 14 candidate gene loci in a family with autosomal dominant osteoarthritis without dysplasia.

Authors:  I Meulenbelt; C Bijkerk; F C Breedveld; P E Slagboom
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

4.  Heteroplasmic point mutations in the human mtDNA control region.

Authors:  K E Bendall; V A Macaulay; J R Baker; B C Sykes
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

5.  Marshall syndrome associated with a splicing defect at the COL11A1 locus.

Authors:  A J Griffith; L K Sprunger; D A Sirko-Osadsa; G E Tiller; M H Meisler; M L Warman
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

6.  Insulin-like growth factor I gene promoter polymorphism, collagen type II alpha1 (COL2A1) gene, and the prevalence of radiographic osteoarthritis: the Rotterdam Study.

Authors:  G Zhai; F Rivadeneira; J J Houwing-Duistermaat; I Meulenbelt; C Bijkerk; A Hofman; J B J van Meurs; A G Uitterlinden; H A P Pols; P E Slagboom; C M van Duijn
Journal:  Ann Rheum Dis       Date:  2004-05       Impact factor: 19.103

7.  Evolution of a repeat sequence in the parathyroid hormone-related peptide gene in primates.

Authors:  Z Pausova; K Morgan; T M Fujiwara; G N Hendy
Journal:  Mamm Genome       Date:  1995-06       Impact factor: 2.957

8.  Evidence that a locus for familial high myopia maps to chromosome 18p.

Authors:  T L Young; S M Ronan; L A Drahozal; S C Wildenberg; A B Alvear; W S Oetting; L D Atwood; D J Wilkin; R A King
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

  8 in total

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