Yokomori N, Kobayashi R, Moore R, Sueyoshi T, Negishi M
Pharmacogenetics Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.
Mol Cell Biol. 1995 Oct;15(10):5355-62. doi: 10.1128/MCB.15.10.5355.
The Cyp 2d-9 gene encodes the male-specific steroid 16 alpha-hydroxylase in mouse liver and shares a conserved regulatory element (-100TTCCGGGC-93) with another male-specific Slp promoter. As shown with the Slp promoter (N. Yokomori, R. Moore, and M. Negishi, Proc. Natl. Acad. Sci. USA 92:1302-1306, 1995), the male-preferential demethylation also occurs at CpG/-97 in the Cyp 2d-9 promoter. The transcription factor which specifically binds to the demethylated element has been purified. The peptide sequences reveal that the factor consists of GABP alpha and GABP beta 1 with Ets and Notch motifs, respectively. Both DNase I footprinting and gel shift assays indicate that the bacterially expressed glutathione S-transferase-GABP fusion proteins bind to the regulatory element only when CpG/-97 is demethylated. Moreover, Cyp 2d-9 promoter is trans-activated by coexpression of GABP proteins in HepG2 cells. Given the additional results that CpG/-50 of the female-specific steroid 15 alpha-hydroxylase (Cyp 2a-4) promoter is preferentially demethylated in the females, the sex-specific expressions of the P450 genes correlate very well with DNA demethylation. We also conclude that GABP is a methylation-sensitive transcription factor and is a potential transcription activator of the male-specific Cyp 2d-9 promoter.
Cyp 2d - 9基因在小鼠肝脏中编码雄性特异性类固醇16α - 羟化酶,并与另一个雄性特异性Slp启动子共享一个保守的调控元件(-100TTCCGGGC - 93)。如Slp启动子所示(N. Yokomori、R. Moore和M. Negishi,《美国国家科学院院刊》92:1302 - 1306,1995),雄性优先去甲基化也发生在Cyp 2d - 9启动子的CpG / - 97处。与去甲基化元件特异性结合的转录因子已被纯化。肽序列显示该因子分别由具有Ets和Notch基序的GABPα和GABPβ1组成。DNase I足迹法和凝胶迁移试验均表明,细菌表达的谷胱甘肽S - 转移酶 - GABP融合蛋白仅在CpG / - 97去甲基化时才与调控元件结合。此外,在HepG2细胞中,GABP蛋白的共表达可反式激活Cyp 2d - 9启动子。鉴于另外的结果表明,雌性特异性类固醇15α - 羟化酶(Cyp 2a - 4)启动子的CpG / - 50在雌性中优先去甲基化,P450基因的性别特异性表达与DNA去甲基化密切相关。我们还得出结论,GABP是一种甲基化敏感的转录因子,是雄性特异性Cyp 2d - 9启动子的潜在转录激活剂。