Literature DB >> 2714801

Organization of the exons coding for pro alpha 1(II) collagen N-propeptide confirms a distinct evolutionary history of this domain of the fibrillar collagen genes.

M W Su1, V Benson-Chanda, H Vissing, F Ramirez.   

Abstract

The organization of the exons coding for the N-terminal portion of human type II procollagen has been determined. Aside from inferring the previously unknown primary structure of type II N-propeptide, this study has revealed that this coding domain of the gene exhibits an organization uniquely distinct from those of type I and type III collagens. This finding substantiates the notion that the N-propeptide coding domains of the fibrillar collagen genes evolved under less stringent selection than those encoding the C-propeptide and triple helical regions.

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Year:  1989        PMID: 2714801     DOI: 10.1016/0888-7543(89)90353-4

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


  7 in total

1.  Nucleotide sequence of the full length cDNA encoding for human type II procollagen.

Authors:  M W Su; B Lee; F Ramirez; M Machado; W Horton
Journal:  Nucleic Acids Res       Date:  1989-11-25       Impact factor: 16.971

2.  The complete intron/exon structure of Ephydatia mülleri fibrillar collagen gene suggests a mechanism for the evolution of an ancestral gene module.

Authors:  J Y Exposito; M van der Rest; R Garrone
Journal:  J Mol Evol       Date:  1993-09       Impact factor: 2.395

Review 3.  A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon.

Authors:  N N Ahmad; D M McDonald-McGinn; E H Zackai; R G Knowlton; D LaRossa; J DiMascio; D J Prockop
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

4.  Co-expression of collagens II and XI and alternative splicing of exon 2 of collagen II in several developing human tissues.

Authors:  M M Sandberg; H E Hirvonen; K J Elima; E I Vuorio
Journal:  Biochem J       Date:  1993-09-01       Impact factor: 3.857

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

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

Authors: 
Journal:  Nucleic Acids Res       Date:  1989-09-12       Impact factor: 16.971

7.  Alternatively spliced type II procollagen mRNAs define distinct populations of cells during vertebral development: differential expression of the amino-propeptide.

Authors:  L J Sandell; N Morris; J R Robbins; M B Goldring
Journal:  J Cell Biol       Date:  1991-09       Impact factor: 10.539

  7 in total

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