Augereau P, Chambon P
EMBO J. 1986 Aug;5(8):1791-7. doi: 10.1002/j.1460-2075.1986.tb04428.x.
The ability of the mouse immunoglobulin heavy chain gene (IgH) enhancer to stimulate in vitro transcription from the adenovirus-2 major late promoter (Ad2MLP) has been investigated. In agreement with the in vivo cell-type specificity of this enhancer, a stimulation can be observed in BJA-B lymphoid B cell, but not in HeLa cell, extracts. Under identical conditions, the Simian virus 40 (SV40) enhancer stimulates transcription in both extracts to approximately the same extent. In addition we have found that a sequence, previously shown to inhibit transcription in vitro in HeLa cell extracts, is also inhibitory in B cell extracts. DNase I footprint and DMS-methylation protection experiments indicate that each cell type contains proteins which bind to specific sequences of the IgH enhancer. The relationship between the binding of these proteins and the preferential activity of the IgH enhancer in B cells is discussed.
对小鼠免疫球蛋白重链基因(IgH)增强子刺激腺病毒2型主要晚期启动子(Ad2MLP)体外转录的能力进行了研究。与该增强子在体内的细胞类型特异性一致,在BJA - B淋巴B细胞提取物中可观察到刺激作用,但在HeLa细胞提取物中则未观察到。在相同条件下,猿猴病毒40(SV40)增强子在两种提取物中刺激转录的程度大致相同。此外,我们发现一个先前显示在HeLa细胞提取物中抑制体外转录的序列,在B细胞提取物中也具有抑制作用。DNase I足迹和DMS甲基化保护实验表明,每种细胞类型都含有与IgH增强子特定序列结合的蛋白质。讨论了这些蛋白质的结合与IgH增强子在B细胞中的优先活性之间的关系。