Rao Rajesh C, Hennig Anne K, Malik Muhammad T A, Chen Dong Feng, Chen Shiming
Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, 660 South Euclid Ave, Campus Box 8096, St. Louis, MO 63110 USA.
J Ocul Biol Dis Infor. 2011 Sep;4(3):121-36. doi: 10.1007/s12177-012-9083-0. Epub 2012 Mar 29.
Epigenetic regulation, including DNA methylation, histone modifications, and chromosomal organization, is emerging as a new layer of transcriptional regulation in retinal development and maintenance. Guided by intrinsic transcription factors and extrinsic signaling molecules, epigenetic regulation can activate and/or repress the expression of specific sets of genes, therefore playing an important role in retinal cell fate specification and terminal differentiation during development as well as maintaining cell function and survival in adults. Here, we review the major findings that have linked these mechanisms to the development and maintenance of retinal structure and function, with a focus on ganglion cells and photoreceptors. The mechanisms of epigenetic regulation are highly complex and vary among different cell types. Understanding the basic principles of these mechanisms and their regulatory pathways may provide new insight into the pathogenesis of retinal diseases associated with transcription dysregulation, and new therapeutic strategies for treatment.
表观遗传调控,包括DNA甲基化、组蛋白修饰和染色体组织,正在成为视网膜发育和维持过程中转录调控的新层面。在内在转录因子和外在信号分子的引导下,表观遗传调控可以激活和/或抑制特定基因集的表达,因此在发育过程中视网膜细胞命运的决定和终末分化以及在成体中维持细胞功能和存活方面发挥着重要作用。在这里,我们综述了将这些机制与视网膜结构和功能的发育及维持联系起来的主要研究发现,重点关注神经节细胞和光感受器。表观遗传调控机制高度复杂,在不同细胞类型中有所不同。了解这些机制的基本原理及其调控途径可能为与转录失调相关的视网膜疾病的发病机制提供新的见解,并为治疗提供新的治疗策略。