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

被引:11
作者
Eyre, S
Roby, P
Wolstencroft, K
Spreckley, K
Aspinwall, R
Bayoumi, R
Al-Gazali, L
Ramesar, R
Beighton, P
Wallis, G
机构
[1] Univ Manchester, Sch Biol Sci, Wellcome Trust Ctr Cell Matrix Res, Manchester M13 9PT, Lancs, England
[2] Univ Manchester, Arthrit Res Campaign, Epidemiol Res Unit, Manchester M13 9PT, Lancs, England
[3] Univ Manchester, Bioinformat Unit, Manchester M13 9PT, Lancs, England
[4] Univ Manchester, Dept Med, Manchester M13 9PT, Lancs, England
[5] Sultan Qaboos Univ, Dept Biochem, Muscat, Oman
[6] United Arab Emirates Univ, Dept Paediat, Al Ain, U Arab Emirates
[7] Univ Cape Town, Dept Human Genet, ZA-7925 Cape Town, South Africa
关键词
D O I
10.1136/jmg.39.9.634
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
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 11 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.
引用
收藏
页码:634 / 638
页数:5
相关论文
共 22 条
[1]
Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance [J].
Al-Gazali, LI ;
Bakalinova, D .
CLINICAL DYSMORPHOLOGY, 1998, 7 (03) :177-184
[2]
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]
SPONDYLOEPIPHYSEAL DYSPLASIA, MILD AUTOSOMAL DOMINANT TYPE IS NOT DUE TO PRIMARY DEFECTS OF TYPE-II COLLAGEN [J].
ANDERSON, IJ ;
TSIPOURAS, P ;
SCHER, C ;
RAMESAR, RS ;
MARTELL, RW ;
BEIGHTON, P .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 37 (02) :272-276
[4]
Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 [J].
Bayoumi, R ;
Saar, K ;
Lee, YA ;
Nürnberg, G ;
Reis, A ;
Nur-E-Kamal, M ;
Al-Gazali, LI .
JOURNAL OF MEDICAL GENETICS, 2001, 38 (06) :369-373
[5]
Prediction of complete gene structures in human genomic DNA [J].
Burge, C ;
Karlin, S .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (01) :78-94
[6]
A human-specific polymorphism in the coding region of the aggrecan gene - Variable number of tandem repeats produce a range of core protein sizes in the general population [J].
Doege, KJ ;
Coulter, SN ;
Meek, LM ;
Maslen, K ;
Wood, JG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (21) :13974-13979
[7]
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda [J].
Gedeon, AK ;
Colley, A ;
Jamieson, R ;
Thompson, EM ;
Rogers, J ;
Sillence, D ;
Tiller, GE ;
Mulley, JC ;
Gécz, J .
NATURE GENETICS, 1999, 22 (04) :400-404
[8]
PROTEOGLYCANS - MANY FORMS AND MANY FUNCTIONS [J].
HARDINGHAM, TE ;
FOSANG, AJ .
FASEB JOURNAL, 1992, 6 (03) :861-870
[9]
Allele-sharing models: LOD scores and accurate linkage tests [J].
Kong, A ;
Cox, NJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (05) :1179-1188
[10]
Kruglyak L, 1996, AM J HUM GENET, V58, P1347