Stone C, Pointon J J, Jazwinska E C, Halliday J W, Powell L W, Robson K J, Monaco A P, Weatherall D J
MRC Molecular Haematology Unit, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UK.
Hum Mol Genet. 1994 Nov;3(11):2043-6.
The gene for hereditary haemochromatosis (HC) is linked to HLA-A and D6S105 on chromosome 6p. Both markers have also been reported to display linkage disequilibrium with the disease. However, their physical localization relative to one another has not been established. We demonstrate by fluorescent in situ hybridisation that D6S105 lies at least 1-2 Mb telomeric of HLA-A. The haemochromatosis critical region extending from proximal of HLA-A to distal of D6S105 is therefore large. To improve the genetic resolution in this region more highly polymorphic markers are required. We have therefore isolated three novel CA dinucleotide repeats close to D6S105. A linkage disequilibrium study, with two of these microsatellites, in HC patients and controls lends support to the conclusion that D6S105 is a close marker to the haemochromatosis gene.
遗传性血色素沉着症(HC)基因与6号染色体短臂上的HLA - A和D6S105相关联。据报道,这两个标记物也与该疾病表现出连锁不平衡。然而,它们彼此之间的物理定位尚未确定。我们通过荧光原位杂交证明,D6S105位于HLA - A端粒至少1 - 2 Mb处。因此,从HLA - A近端延伸至D6S105远端的血色素沉着症关键区域很大。为了提高该区域的遗传分辨率,需要更多高度多态性的标记物。因此,我们在靠近D6S105的位置分离出了三个新的CA二核苷酸重复序列。对其中两个微卫星与HC患者及对照进行的连锁不平衡研究支持了D6S105是血色素沉着症基因紧密标记物这一结论。