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Study of CYP2D6 gene in children with autoimmune hepatitis and P450 IID6 autoantibodies.

机译:儿童自身免疫性肝炎和P450 IID6自身抗体的CYP2D6基因研究。

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摘要

Cytochrome P450 IID6 is an autoantigen recognized by the sera of children affected with a subtype of autoimmune hepatitis. It was hypothesized that a mutation in the CYP2D6 gene could explain the autoimmune response in these patients. To examine this question, genomic DNA from peripheral lymphocytes (n = 9) and liver (n = 1) of 10 patients with anti-LKM-1 antibody was analysed by Southern blot for genetic association studies between a particular CYP2D6 haplotype and autoimmune hepatitis. In addition, a region of CYP2D6, from the same genomic DNA, was amplified by polymerase chain reaction (PCR) and digested by BstNI, in a search for the most prevalent 29B mutation, described in subjects who do not express the P450 IID6. Total RNA and proteins, prepared from the liver of an anti-LKM-1+ patient, were analysed by Northern and Western (immunoblot) blots respectively. Our results do not reveal any major structural change in the DNA of this patient at the CYP2D6 locus that could explain their autoimmune response. Corroborating this observation, no changes were noted either in P450 IID6 mRNA size or in the corresponding protein. However, these data do not exclude the possibility of subtle changes in the protein due to point mutations in critical regions that might trigger an autoimmune response.
机译:细胞色素P450 IID6是一种自身抗原,被患有自身免疫性肝炎亚型的儿童的血清识别。假设CYP2D6基因突变可以解释这些患者的自身免疫反应。为了检查这个问题,通过Southern blot分析了10名抗LKM-1抗体患者外周血淋巴细胞(n = 9)和肝脏(n = 1)的基因组DNA,以进行特定CYP2D6单倍型与自身免疫性肝炎之间的遗传关联研究。此外,为了寻找最普遍的29B突变,对不表达P450 IID6的受试者进行了描述,通过聚合酶链反应(PCR)扩增了来自同一基因组DNA的CYP2D6区域,并通过BstNI对其进行了消化。从抗LKM-1 +患者的肝脏中制备的总RNA和蛋白质分别通过Northern和Western(免疫印迹)印迹进行分析。我们的结果未显示该患者在CYP2D6基因座处的DNA发生任何重大结构变化,可解释其自身免疫反应。证实该观察结果,P450 IID6 mRNA大小或相应蛋白质均未发现变化。但是,这些数据并未排除由于可能触发自身免疫反应的关键区域中的点突变而导致蛋白质细微变化的可能性。

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