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皮质神经发生过程中依赖ATP的染色质重塑

ATP-Dependent Chromatin Remodeling During Cortical Neurogenesis.

作者信息

Sokpor Godwin, Castro-Hernandez Ricardo, Rosenbusch Joachim, Staiger Jochen F, Tuoc Tran

机构信息

Institute for Neuroanatomy, University Medical Center, Georg-August-University Goettingen, Goettingen, Germany.

DFG Center for Nanoscale Microscopy and Molecular Physiology of the Brain, Goettingen, Germany.

出版信息

Front Neurosci. 2018 Apr 9;12:226. doi: 10.3389/fnins.2018.00226. eCollection 2018.

DOI:10.3389/fnins.2018.00226
PMID:29686607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5900035/
Abstract

The generation of individual neurons (neurogenesis) during cortical development occurs in discrete steps that are subtly regulated and orchestrated to ensure normal histogenesis and function of the cortex. Notably, various gene expression programs are known to critically drive many facets of neurogenesis with a high level of specificity during brain development. Typically, precise regulation of gene expression patterns ensures that key events like proliferation and differentiation of neural progenitors, specification of neuronal subtypes, as well as migration and maturation of neurons in the developing cortex occur properly. ATP-dependent chromatin remodeling complexes regulate gene expression through utilization of energy from ATP hydrolysis to reorganize chromatin structure. These chromatin remodeling complexes are characteristically multimeric, with some capable of adopting functionally distinct conformations via subunit reconstitution to perform specific roles in major aspects of cortical neurogenesis. In this review, we highlight the functions of such chromatin remodelers during cortical development. We also bring together various proposed mechanisms by which ATP-dependent chromatin remodelers function individually or in concert, to specifically modulate vital steps in cortical neurogenesis.

摘要

在皮质发育过程中,单个神经元的产生(神经发生)以离散的步骤进行,这些步骤受到精细调节和协调,以确保皮质正常的组织发生和功能。值得注意的是,已知各种基因表达程序在脑发育过程中以高度特异性严格驱动神经发生的许多方面。通常,基因表达模式的精确调节可确保神经祖细胞的增殖和分化、神经元亚型的特化以及发育中的皮质中神经元的迁移和成熟等关键事件正常发生。ATP依赖的染色质重塑复合物通过利用ATP水解产生的能量来重组染色质结构,从而调节基因表达。这些染色质重塑复合物通常是多聚体,有些能够通过亚基重组形成功能不同的构象,以在皮质神经发生的主要方面发挥特定作用。在本综述中,我们重点介绍了此类染色质重塑因子在皮质发育过程中的功能。我们还汇总了各种提出的机制,通过这些机制,ATP依赖的染色质重塑因子单独或协同作用,以特异性调节皮质神经发生中的关键步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/280e/5900035/45caab34d2e7/fnins-12-00226-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/280e/5900035/dee96cda5c85/fnins-12-00226-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/280e/5900035/3c7f0db3fb87/fnins-12-00226-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/280e/5900035/45caab34d2e7/fnins-12-00226-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/280e/5900035/dee96cda5c85/fnins-12-00226-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/280e/5900035/3c7f0db3fb87/fnins-12-00226-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/280e/5900035/45caab34d2e7/fnins-12-00226-g0003.jpg

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