Department of Genetics, The Institute of Life Sciences, The Hebrew University of Jerusalem-Edmond J. Safra Campus, Jerusalem, Israel.
Nucleus. 2012 Sep-Oct;3(5):433-41. doi: 10.4161/nucl.21481. Epub 2012 Aug 15.
Polyglutamine (PolyQ)-related diseases are dominant late-onset genetic disorders that are manifested by progressive neurodegeneration, leading to behavioral and physical impairments. An increased body of evidence suggests that chromatin structure and epigenetic regulation are involved in disease pathology. PolyQ diseases often display an aberrant transcriptional regulation due to the disrupted function of histone-modifying complexes and altered interactions of the polyQ-extended proteins with chromatin-related factors. In this review we describe recent findings relating to the role of chromatin in polyQ diseases. We discuss the involvement of epigenetic-related factors and chromatin structure in genomic instability of CAG repeats; we describe changes in the expression and regulation of chromatin-related enzymes and in the levels and patterns of histone modifications in disease state; we illustrate the potential beneficial effects of different histone deacetylase (HDAC) inhibitors for the treatment of polyQ diseases, and we end by describing the potential use of human pluripotent stem cells and their differentiated derivatives for modeling polyQ diseases in vitro. Taken together, these accumulating studies strongly suggest that disrupted chromatin regulation may be directly involved with the pathophysiology of polyQ-related diseases.
多聚谷氨酰胺(PolyQ)相关性疾病是显性迟发性遗传疾病,表现为进行性神经退行性变,导致行为和身体功能障碍。越来越多的证据表明,染色质结构和表观遗传调控参与了疾病的发病机制。由于组蛋白修饰复合物功能紊乱以及多聚谷氨酰胺延伸蛋白与染色质相关因子的相互作用改变,PolyQ 疾病通常表现出异常的转录调控。在这篇综述中,我们描述了与染色质在 PolyQ 疾病中的作用相关的最新发现。我们讨论了与表观遗传相关的因素和染色质结构在 CAG 重复不稳定中的作用;我们描述了染色质相关酶的表达和调节以及疾病状态下组蛋白修饰水平和模式的变化;我们说明了不同组蛋白去乙酰化酶(HDAC)抑制剂在治疗 PolyQ 疾病方面的潜在有益作用,并最后描述了人类多能干细胞及其分化衍生物在体外模拟 PolyQ 疾病的潜在用途。综上所述,这些不断积累的研究强烈表明,染色质调控的破坏可能直接参与 PolyQ 相关疾病的病理生理学。