Lichtenstein M, Keini G, Cedar H, Bergman Y
Hubert H. Humphrey Center for Experimental Medicine and Cancer Research, Hebrew University, Hadassah Medical School, Jerusalem, Israel.
Cell. 1994 Mar 11;76(5):913-23. doi: 10.1016/0092-8674(94)90365-4.
We studied the molecular mechanism of demethylation and its role in kappa chain gene regulation. Following transfection into B cell cultures, this gene undergoes regional demethylation in a process that is developmentally regulated in a lineage- and stage-specific manner. Although a germline V kappa promoter is not required for the demodification activity, a fragment containing the intronic kappa chain transcriptional enhancer and the nearby matrix attachment region is essential. In its natural location downstream to the J kappa 5 sequence, this element induces bidirectional demodification of plasmid constructs in a distance- and orientation-independent manner. When this enhancer is placed in an upstream position, however, the kappa gene remains modified and transcriptionally inactive, demonstrating that demethylation is required for kappa chain activation. These studies suggest that the kappa enhancer plays a dual role in regulating B cell differentiation by inducing demethylation and by promoting tissue-specific transcription.
我们研究了去甲基化的分子机制及其在κ链基因调控中的作用。转染至B细胞培养物后,该基因在一个以谱系和阶段特异性方式进行发育调控的过程中发生区域去甲基化。虽然种系Vκ启动子对于去修饰活性并非必需,但包含内含子κ链转录增强子和附近基质附着区域的片段却是至关重要的。在其天然位于Jκ5序列下游的位置,该元件以与距离和方向无关的方式诱导质粒构建体的双向去修饰。然而,当该增强子置于上游位置时,κ基因仍保持甲基化且转录无活性,这表明去甲基化是κ链激活所必需的。这些研究表明,κ增强子通过诱导去甲基化和促进组织特异性转录在调节B细胞分化中发挥双重作用。