Oksenberg J R, Gaiser C N, Cavalli-Sforza L L, Steinman L
Department of Neurology, Stanford University School of Medicine, California 94305.
Hum Immunol. 1988 Jun;22(2):111-21. doi: 10.1016/0198-8859(88)90041-9.
Polymorphic markers for the human T-cell receptor (TcR) genes are described. With a TcR beta-chain probe, polymorphic allelic fragments of 5.4 and 1.8 kb were detected in KpnI digests, and fragments of 12.5 and 11.5 kb were seen in the BglII digests. Polymorphism in alpha chain genes was observed in TaqI-digested DNA samples with bands at 10.2 and 6.2-2.1 kb. Mendelian codominant inheritance for all three polymorphisms was confirmed in family studies. The gene frequencies for these alleles were determined in a sample of 70 normal unrelated Caucasian individuals, and were shown to be in Hardy-Weinberg equilibrium. There were no significant differences in the frequency of these polymorphic alpha and beta alleles between patients with multiple sclerosis and patients with myasthenia gravis as compared to a panel of control healthy individuals.
描述了人类T细胞受体(TcR)基因的多态性标记。用TcRβ链探针,在KpnI酶切物中检测到5.4和1.8 kb的多态性等位基因片段,在BglII酶切物中可见12.5和11.5 kb的片段。在TaqI酶切的DNA样品中观察到α链基因的多态性,条带位于10.2和6.2 - 2.1 kb处。在家族研究中证实了所有这三种多态性的孟德尔共显性遗传。在70名正常无亲缘关系的白种人个体样本中确定了这些等位基因的基因频率,并显示其处于哈迪-温伯格平衡。与一组健康对照个体相比,多发性硬化症患者和重症肌无力患者中这些多态性α和β等位基因的频率没有显著差异。