Eyre S, Roby P, Wolstencroft K, Spreckley K, Aspinwall R, Bayoumi R, Al-Gazali L, Ramesar R, Beighton P, Wallis G
The Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, Manchester, UK.
J Med Genet. 2002 Sep;39(9):634-8. doi: 10.1136/jmg.39.9.634.
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.
我们研究了一个患有常染色体显性脊椎骨骺发育不良(SED)的家族,其特征为身材矮小和严重的过早退行性关节病。先前的研究已排除该病症与II型胶原基因位点之间的连锁关系。在此,我们报告该疾病与位于15号染色体长臂上标记D15S979和D15S1004之间的一个位点存在连锁关系。根据当前的连锁图谱和序列数据,该位点包括聚集蛋白聚糖基因(AGC1)的位点。然而,我们来自SED家族的连锁数据表明,AGC1定位于D15S979近端的一个位点。来自另一个患有常染色体隐性多发性骨骺发育不良且也定位于SED位点的家族的连锁数据进一步支持了AGC1的这个近端位置。因此,在这两个家族中,AGC1都被排除为候选基因。