Literature DB >> 12205105

Identification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate gene.

S Eyre1, P Roby, K Wolstencroft, K Spreckley, R Aspinwall, R Bayoumi, L Al-Gazali, R Ramesar, P Beighton, G Wallis.   

Abstract

We have investigated a family with an autosomal dominant form of spondyloepiphyseal dysplasia (SED) characterised by short stature and severe premature degenerative arthropathy. Previous studies have excluded linkage between this condition and the locus for the type II collagen gene. Here we report the identification of linkage between this disorder and a locus on the long arm of chromosome 15 between markers D15S979 and D15S1004. According to current linkage maps and sequence data, this locus includes that of the aggrecan gene (AGC1). Our linkage data from the SED family show, however, that AGC1 maps to a locus that is proximal to D15S979. This proximal location for AGC1 is further supported by linkage data from a second family with an autosomal recessive form of multiple epiphyseal dysplasia that also maps to the SED locus. In both families AGC1 is therefore excluded as a candidate gene.

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Year:  2002        PMID: 12205105      PMCID: PMC1735219          DOI: 10.1136/jmg.39.9.634

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  20 in total

Review 1.  Proteoglycans: many forms and many functions.

Authors:  T E Hardingham; A J Fosang
Journal:  FASEB J       Date:  1992-02-01       Impact factor: 5.191

2.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

3.  Structure of the human aggrecan gene: exon-intron organization and association with the protein domains.

Authors:  W B Valhmu; G D Palmer; P A Rivers; S Ebara; J F Cheng; S Fischer; A Ratcliffe
Journal:  Biochem J       Date:  1995-07-15       Impact factor: 3.857

4.  Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda.

Authors:  A K Gedeon; A Colley; R Jamieson; E M Thompson; J Rogers; D Sillence; G E Tiller; J C Mulley; J Gécz
Journal:  Nat Genet       Date:  1999-08       Impact factor: 38.330

5.  Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26.

Authors:  R Bayoumi; K Saar; Y A Lee; G Nürnberg; A Reis; M Nur-E-Kamal; L I Al-Gazali
Journal:  J Med Genet       Date:  2001-06       Impact factor: 6.318

6.  cDNA cloning of chick cartilage chondroitin sulfate (aggrecan) core protein and identification of a stop codon in the aggrecan gene associated with the chondrodystrophy, nanomelia.

Authors:  H Li; N B Schwartz; B M Vertel
Journal:  J Biol Chem       Date:  1993-11-05       Impact factor: 5.157

7.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

8.  SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia.

Authors:  W A Sweetman; B Rash; B Sykes; P Beighton; J T Hecht; B Zabel; J T Thomas; R Boot-Handford; M E Grant; G A Wallis
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

9.  Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene.

Authors:  H Watanabe; K Kimata; S Line; D Strong; L Y Gao; C A Kozak; Y Yamada
Journal:  Nat Genet       Date:  1994-06       Impact factor: 38.330

10.  Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagen.

Authors:  I J Anderson; P Tsipouras; C Scher; R S Ramesar; R W Martell; P Beighton
Journal:  Am J Med Genet       Date:  1990-10
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  4 in total

1.  A whole genome linkage scan for QTLs underlying peak bone mineral density.

Authors:  F Zhang; P Xiao; F Yang; H Shen; D-H Xiong; H-Y Deng; C J Papasian; B M Drees; J J Hamilton; R R Recker; H-W Deng
Journal:  Osteoporos Int       Date:  2007-09-19       Impact factor: 4.507

2.  A mutation in the variable repeat region of the aggrecan gene (AGC1) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritis.

Authors:  Lindsay Gleghorn; Rajkumar Ramesar; Peter Beighton; Gillian Wallis
Journal:  Am J Hum Genet       Date:  2005-07-22       Impact factor: 11.025

3.  A missense mutation in the aggrecan C-type lectin domain disrupts extracellular matrix interactions and causes dominant familial osteochondritis dissecans.

Authors:  Eva-Lena Stattin; Fredrik Wiklund; Karin Lindblom; Patrik Onnerfjord; Björn-Anders Jonsson; Yelverton Tegner; Takako Sasaki; André Struglics; Stefan Lohmander; Niklas Dahl; Dick Heinegård; Anders Aspberg
Journal:  Am J Hum Genet       Date:  2010-02-04       Impact factor: 11.025

4.  ACAN mutations as a cause of familial short stature.

Authors:  Sumito Dateki
Journal:  Clin Pediatr Endocrinol       Date:  2017-07-27
  4 in total

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