Alexander J M, Lomvardas S
Department of Anatomy, University of California, San Francisco, San Francisco, CA 94158, USA.
Department of Anatomy, University of California, San Francisco, San Francisco, CA 94158, USA.
Neuroscience. 2014 Apr 4;264:39-50. doi: 10.1016/j.neuroscience.2014.01.044. Epub 2014 Jan 31.
The nervous system of higher organisms is characterized by an enormous diversity of cell types that function in concert to carry out a myriad of neuronal functions. Differences in connectivity, and subsequent physiology of the connected neurons, are a result of differences in transcriptional programs. The extraordinary complexity of the nervous system requires an equally complex regulatory system. It is well established that transcription factor combinations and the organization of cis-regulatory sequences control commitment to differentiation programs and preserve a nuclear plasticity required for neuronal functions. However, an additional level of regulation is provided by epigenetic controls. Among various epigenetic processes, nuclear organization and the control of genome architecture emerge as an efficient and powerful form of gene regulation that meets the unique needs of the post-mitotic neuron. Here, we present an outline of how nuclear architecture affects transcription and provide examples from the recent literature where these principles are used by the nervous system.
高等生物的神经系统具有细胞类型的巨大多样性,这些细胞协同发挥作用以执行无数的神经元功能。连接性的差异以及相连神经元随后的生理学差异是转录程序差异的结果。神经系统的非凡复杂性需要同样复杂的调节系统。转录因子组合和顺式调节序列的组织控制着分化程序的定向并维持神经元功能所需的核可塑性,这一点已得到充分证实。然而,表观遗传控制提供了另一层次的调节。在各种表观遗传过程中,核组织和基因组结构的控制作为一种有效且强大的基因调节形式出现,满足了有丝分裂后神经元的独特需求。在这里,我们概述了核结构如何影响转录,并提供了近期文献中的实例,说明神经系统如何运用这些原理。