Eivazova Elvira R, Aune Thomas M
Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Proc Natl Acad Sci U S A. 2004 Jan 6;101(1):251-6. doi: 10.1073/pnas.0303919101. Epub 2003 Dec 22.
Gene expression and silencing in eukaryotic systems can be controlled by regulatory elements acting over a distance. Here, we analyze chromatin conformation of the 24-kb region of the Ifng gene during CD4(+) T helper (Th) cell differentiation. We find that chromatin within this region is a highly flexible structure that undergoes dynamic changes during the course of transcriptional activation and silencing of the Ifng gene. Each Th subset displays a common core conformation in this gene region and unique features that distinguish neutral and effector Th1 and Th2 lineages. This chromatin configuration brings distal regions into close proximity to the gene. Th1 cells that produce high levels of IFN-gamma display the most open conformation. In contrast, IFN-gamma silent Th2 cells have a tightly closed conformation. Therefore, we postulate that there is a direct structure-function relationship between the spatial organization of the chromatin around the Ifng gene and its transcriptional potential.
真核系统中的基因表达和沉默可由远距离作用的调控元件控制。在此,我们分析了Ifng基因24 kb区域在CD4(+)辅助性T(Th)细胞分化过程中的染色质构象。我们发现该区域内的染色质是一种高度灵活的结构,在Ifng基因转录激活和沉默过程中会发生动态变化。每个Th亚群在该基因区域都呈现出共同的核心构象以及区分中性和效应性Th1和Th2谱系的独特特征。这种染色质构型使远端区域与基因紧密靠近。产生高水平IFN-γ的Th1细胞呈现出最开放的构象。相反,IFN-γ沉默的Th2细胞具有紧密闭合的构象。因此,我们推测Ifng基因周围染色质的空间组织与其转录潜能之间存在直接的结构-功能关系。