LINKAGE OF THE GENE THAT ENCODES THE ALPHA-1 CHAIN OF TYPE-V COLLAGEN (COL5A1) TO TYPE-II EHLERS-DANLOS SYNDROME (EDS-II)

被引:37
作者
LOUGHLIN, J
IRVEN, C
HARDWICK, LJ
BUTCHER, S
WALSH, S
WORDSWORTH, P
SYKES, B
机构
[1] JOHN RADCLIFFE HOSP,NUFFIELD DEPT CLIN MED,OXFORD OX3 9DU,ENGLAND
[2] UNIV OXFORD,WELLCOME TRUST CTR HUMAN GENET,NUFFIELD DEPT CLIN MED,OXFORD OX3 7BN,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1093/hmg/4.9.1649
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ehlers-Danlos syndrome (EDS) is a group of heritable disorders of connective tissue with skin, ligaments and blood vessels being the main sites affected. The commonest variant (EDS II) exhibits an autosomal dominant mode of inheritance and is characterized by joint hypermobility, cigarette paper scars, lax skin and excessive bruising. As yet no gene has been linked to EDS II, nor has linkage been established to a specific region of the genome. However, several candidate genes encoding proteins of the extracellular matrix have been excluded. Using an intragenic simple sequence repeat polymorphism, we report linkage of the COL5A1 gene, which encodes the alpha 1 (V) chain of type V collagen, to EDS II. A maximum LOD score (Z(max)) for linkage of 8.3 at theta = 0.00 was generated for a single large pedigree.
引用
收藏
页码:1649 / 1651
页数:3
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