Swammerdam Institute for Life Sciences, Netherlands Institute for Systems Biology, University of Amsterdam, Amsterdam, The Netherlands.
PLoS One. 2013 Jul 23;8(7):e69347. doi: 10.1371/journal.pone.0069347. Print 2013.
Methyl-CpG-binding protein 2 (MeCP2) is generally considered to act as a transcriptional repressor, whereas recent studies suggest that MeCP2 is also involved in transcription activation. To gain insight into this dual function of MeCP2, we assessed the impact of MeCP2 on higher-order chromatin structure in living cells using mammalian cell systems harbouring a lactose operator and reporter gene-containing chromosomal domain to assess the effect of lactose repressor-tagged MeCP2 (and separate MeCP2 domains) binding in living cells. Our data reveal that targeted binding of MeCP2 elicits extensive chromatin unfolding. MeCP2-induced chromatin unfolding is triggered independently of the methyl-cytosine-binding domain. Interestingly, MeCP2 binding triggers the loss of HP1γ at the chromosomal domain and an increased HP1γ mobility, which is not observed for HP1α and HP1β. Surprisingly, MeCP2-induced chromatin unfolding is not associated with transcriptional activation. Our study suggests a novel role for MeCP2 in reorganizing chromatin to facilitate a switch in gene activity.
甲基化 CpG 结合蛋白 2(MeCP2)通常被认为是一种转录抑制因子,而最近的研究表明,MeCP2 也参与转录激活。为了深入了解 MeCP2 的这种双重功能,我们使用含有乳糖操纵子和报告基因的染色体结构域的哺乳动物细胞系统,评估了 MeCP2 对活细胞中高级染色质结构的影响,以评估乳糖抑制物标记的 MeCP2(和单独的 MeCP2 结构域)在活细胞中的结合效应。我们的数据表明,MeCP2 的靶向结合会引起广泛的染色质解折叠。MeCP2 诱导的染色质解折叠是独立于甲基胞嘧啶结合结构域触发的。有趣的是,MeCP2 结合会导致染色体结构域上的 HP1γ 丢失和 HP1γ 流动性增加,而 HP1α 和 HP1β 则不会观察到这种现象。令人惊讶的是,MeCP2 诱导的染色质解折叠与转录激活无关。我们的研究表明,MeCP2 在重新组织染色质以促进基因活性转换方面具有新的作用。