Rahman Samir, Roussos Panos
Center for Disease Neurogenomics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Neurosci Insights. 2024 Oct 29;19:26331055241293455. doi: 10.1177/26331055241293455. eCollection 2024.
The human brain contains multiple cell types that are spatially organized into functionally distinct regions. The proper development of the brain requires complex gene regulation mechanisms in both neurons and the non-neuronal cell types that support neuronal function. Studies across the last decade have discovered that the 3D nuclear organization of the genome is instrumental in the regulation of gene expression in the diverse cell types of the brain. In this review, we describe the fundamental biochemical mechanisms that regulate the 3D genome, and comprehensively describe in vitro and ex vivo studies on mouse and human brain development that have characterized the roles of the 3D genome in gene regulation. We highlight the significance of the 3D genome in linking distal enhancers to their target promoters, which provides insights on the etiology of psychiatric and neurological disorders, as the genetic variants associated with these disorders are primarily located in noncoding regulatory regions. We also describe the molecular mechanisms that regulate chromatin folding and gene expression in neurons. Furthermore, we describe studies with an evolutionary perspective, which have investigated features that are conserved from mice to human, as well as human gained 3D chromatin features. Although most of the insights on disease and molecular mechanisms have been obtained from bulk 3C based experiments, we also highlight other approaches that have been developed recently, such as single cell 3C approaches, as well as non-3C based approaches. In our future perspectives, we highlight the gaps in our current knowledge and emphasize the need for 3D genome engineering and live cell imaging approaches to elucidate mechanisms and temporal dynamics of chromatin interactions, respectively.
人类大脑包含多种细胞类型,这些细胞在空间上组织成功能不同的区域。大脑的正常发育需要神经元和支持神经元功能的非神经元细胞类型中复杂的基因调控机制。过去十年的研究发现,基因组的三维核组织有助于调节大脑中各种细胞类型的基因表达。在这篇综述中,我们描述了调节三维基因组的基本生化机制,并全面描述了关于小鼠和人类大脑发育的体外和体内研究,这些研究已经阐明了三维基因组在基因调控中的作用。我们强调三维基因组在将远端增强子与其靶启动子连接方面的重要性,这为精神疾病和神经疾病的病因学提供了见解,因为与这些疾病相关的遗传变异主要位于非编码调控区域。我们还描述了调节神经元中染色质折叠和基因表达的分子机制。此外,我们从进化的角度描述了相关研究,这些研究调查了从小鼠到人类保守的特征以及人类获得的三维染色质特征。尽管关于疾病和分子机制的大多数见解是通过基于批量3C的实验获得的,但我们也强调了最近开发的其他方法,如单细胞3C方法以及非基于3C的方法。在我们对未来的展望中,我们强调了当前知识中的差距,并强调了分别需要三维基因组工程和活细胞成像方法来阐明染色质相互作用的机制和时间动态。