Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Buenos Aires, Argentina.
CONICET-Universidad de Buenos Aires, IFIBYNE, Buenos Aires, Argentina.
Sci Rep. 2017 Jul 24;7(1):6219. doi: 10.1038/s41598-017-06676-0.
The distribution of the transcription machinery among different sub-nuclear domains raises the question on how the architecture of the nucleus modulates the transcriptional response. Here, we used fluorescence fluctuation analyses to quantitatively explore the organization of the glucocorticoid receptor (GR) in the interphase nucleus of living cells. We found that this ligand-activated transcription factor diffuses within the nucleus and dynamically interacts with bodies enriched in the coregulator NCoA-2, DNA-dependent foci and chromatin targets. The distribution of the receptor among the nuclear compartments depends on NCoA-2 and the conformation of the receptor as assessed with synthetic ligands and GR mutants with impaired transcriptional abilities. Our results suggest that the partition of the receptor in different nuclear reservoirs ultimately regulates the concentration of receptor available for the interaction with specific targets, and thus has an impact on transcription regulation.
转录机制在不同核亚区的分布提出了一个问题,即细胞核的结构如何调节转录反应。在这里,我们使用荧光波动分析定量研究了糖皮质激素受体(GR)在活细胞间期核中的组织。我们发现,这种配体激活的转录因子在核内扩散,并与富含共激活因子 NCoA-2、DNA 依赖性焦点和染色质靶标的体动态相互作用。受体在核区室之间的分布取决于 NCoA-2 和受体的构象,这可以通过合成配体和转录能力受损的 GR 突变体来评估。我们的结果表明,受体在不同核储库中的分配最终调节了与特定靶标相互作用的受体的浓度,从而对转录调控产生影响。