Yamamoto A M, Mura C, Morales M G, Bernard O, Krishnamoorthy R, Alvarez F
INSERM U 56, Hôpital de Bicêtre, Kremlin-Bicêtre, France.
Clin Exp Immunol. 1992 Feb;87(2):251-5. doi: 10.1111/j.1365-2249.1992.tb02983.x.
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.
细胞色素P450 IID6是自身免疫性肝炎一种亚型患儿血清所识别的自身抗原。据推测,CYP2D6基因的突变可以解释这些患者的自身免疫反应。为研究这一问题,采用Southern印迹法对10例抗LKM-1抗体阳性患者外周淋巴细胞(n = 9)和肝脏(n = 1)的基因组DNA进行分析,以研究特定CYP2D6单倍型与自身免疫性肝炎之间的遗传关联性。此外,采用聚合酶链反应(PCR)对同一基因组DNA中的CYP2D6区域进行扩增,并用BstNI酶切,以寻找在不表达P450 IID6的个体中描述的最常见的29B突变。分别采用Northern印迹法和Western(免疫印迹)法对1例抗LKM-1抗体阳性患者肝脏制备的总RNA和蛋白质进行分析。我们的结果未显示该患者CYP2D6基因座DNA有任何可解释其自身免疫反应的主要结构变化。与此观察结果一致,P450 IID6 mRNA大小或相应蛋白质均未发现变化。然而,这些数据并不排除关键区域点突变导致蛋白质细微变化从而引发自身免疫反应的可能性。