Goodship J, Malcolm S, Lau Y L, Pembrey M E, Levinsky R J
Department of Immunology, Institute of Child Health, London.
Lancet. 1988 Apr 2;1(8588):729-32. doi: 10.1016/s0140-6736(88)91537-1.
Analysis of X chromosome inactivation in T-lymphocyte DNA from two obligate carriers of X-linked severe combined immunodeficiency showed a non-random pattern. This method was then used to establish carrier status in at-risk females in X-linked pedigrees. It was further used to differentiate between X-linked and autosomal recessive inheritance of the disease when the mode of inheritance was not clear from the pedigree. In addition, a mother of a boy affected by the sporadic form of the disease was found to have non-random X inactivation in her T lymphocytes and she is therefore a carrier of the X-linked disease.
对两名X连锁严重联合免疫缺陷症的 obligate 携带者的T淋巴细胞DNA进行的X染色体失活分析显示出一种非随机模式。然后该方法被用于确定X连锁家系中有风险女性的携带者状态。当系谱中疾病的遗传模式不明确时,它还被进一步用于区分该疾病的X连锁和常染色体隐性遗传。此外,一名患有散发性该疾病男孩的母亲在其T淋巴细胞中被发现有非随机X失活现象,因此她是该X连锁疾病的携带者。