Literature DB >> 2753125

Structural analyses of the polymorphic area in type II collagen gene.

M Vikkula1, L Peltonen.   

Abstract

The structure of type II collagen gene is extremely well conserved but contains a cluster of high frequency polymorphisms in a 2.2 kb area. Here we report the nucleotide sequence of this DNA area, essential for the PCR-facilitated RFLP-analyses of this gene. In the structural analyses we found four differences in the deduced human amino acid sequence when compared to the published bovine amino acid sequence. The donor and acceptor signals and branch point signals required for the splicing events were in agreement with mammalian consensus sequences. The frequency of inverted repeats which could provoke the DNA strand to loop formation and consequently to deletion mutations did not differ from that found in other sequenced genes coding for fibrillar collagens. mutations did not differ from that found in other sequenced genes coding for fibrillar collagens.

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Year:  1989        PMID: 2753125     DOI: 10.1016/0014-5793(89)80713-6

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  5 in total

1.  PCR detection of a HindIII polymorphism in the human gene for type II procollagen (COL2A1).

Authors:  T Tsuneyoshi; B P Sokolov; D J Prockop
Journal:  Nucleic Acids Res       Date:  1991-08-25       Impact factor: 16.971

2.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1989-11-25       Impact factor: 16.971

3.  Conservation of the sizes of 53 introns and over 100 intronic sequences for the binding of common transcription factors in the human and mouse genes for type II procollagen (COL2A1).

Authors:  L Ala-Kokko; A P Kvist; M Metsäranta; K I Kivirikko; B de Crombrugghe; D J Prockop; E Vuorio
Journal:  Biochem J       Date:  1995-06-15       Impact factor: 3.857

4.  Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)

Authors:  J Körkkö; P Ritvaniemi; L Haataja; H Kääriäinen; K I Kivirikko; D J Prockop; L Ala-Kokko
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

5.  Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.

Authors:  L Ala-Kokko; C T Baldwin; R W Moskowitz; D J Prockop
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

  5 in total

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