Trotter Kevin W, Archer Trevor K
Chromatin and Gene Expression Section, Laboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, National Institutes of Health, 111 T.W. Alexander Drive, P.O. Box 12233 (MD C4-06), Research Triangle Park, NC 27709, USA.
Mol Cell Endocrinol. 2007 Feb;265-266:162-7. doi: 10.1016/j.mce.2006.12.015. Epub 2007 Jan 19.
Eukaryotic genetic information is stored within the association of DNA and histone proteins resulting in a dynamic polymer called chromatin. The fundamental structural unit of chromatin is the nucleosome which consists of approximately 146 bp of DNA wrapped around an octamer of histones containing two copies each of four core histones, H2A, H2B, H3 and H4. It is this DNA/protein fiber that transcription factors and other agents of chromatin metabolism must access and regulate. We have developed model systems to study the mechanisms by which steroid receptors control physiological activities by regulating gene expression within a higher order chromatin organization. Our studies have focused on the glucocorticoid receptor and its ability to remodel chromatin which is mediated by the BRG1 complex. Using novel cell systems, we demonstrate that GR-mediated transactivation from chromatin templates requires BRG1 remodeling activity and that other ATP-dependent remodeling proteins cannot substitute for this activity.
真核生物的遗传信息存储于DNA与组蛋白的结合物中,形成一种名为染色质的动态聚合物。染色质的基本结构单元是核小体,它由约146个碱基对的DNA缠绕在一个组蛋白八聚体上组成,该八聚体包含四种核心组蛋白(H2A、H2B、H3和H4)各两个拷贝。正是这种DNA/蛋白质纤维,转录因子和染色质代谢的其他因子必须能够接触并对其进行调控。我们已经开发出模型系统,以研究类固醇受体通过在更高层次的染色质组织中调节基因表达来控制生理活动的机制。我们的研究聚焦于糖皮质激素受体及其重塑染色质的能力,这一过程由BRG1复合体介导。利用新型细胞系统,我们证明了从染色质模板进行的GR介导的反式激活需要BRG1重塑活性,并且其他依赖ATP的重塑蛋白无法替代这种活性。