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表观遗传调控的纤毛发生和细胞周期调控及其转化潜力。

Epigenetically Mediated Ciliogenesis and Cell Cycle Regulation, and Their Translational Potential.

机构信息

Department of Internal Medicine, Mayo Clinic, Rochester, MN 55905, USA.

Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Cells. 2021 Jul 2;10(7):1662. doi: 10.3390/cells10071662.

DOI:10.3390/cells10071662
PMID:34359832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8307023/
Abstract

Primary cilia biogenesis has been closely associated with cell cycle progression. Cilia assemble when cells exit the cell cycle and enter a quiescent stage at the post-mitosis phase, and disassemble before cells re-enter a new cell cycle. Studies have focused on how the cell cycle coordinates with the cilia assembly/disassembly process, and whether and how cilia biogenesis affects the cell cycle. Appropriate regulation of the functions and/or expressions of ciliary and cell-cycle-associated proteins is pivotal to maintaining bodily homeostasis. Epigenetic mechanisms, including DNA methylation and histone/chromatin modifications, are involved in the regulation of cell cycle progression and cilia biogenesis. In this review, first, we discuss how epigenetic mechanisms regulate cell cycle progression and cilia biogenesis through the regulation of DNA methylation and chromatin structures, to either promote or repress the transcription of genes associated with those processes and the modification of cytoskeleton network, including microtubule and actin. Next, we discuss the crosstalk between the cell cycle and ciliogenesis, and the involvement of epigenetic regulators in this process. In addition, we discuss cilia-dependent signaling pathways in cell cycle regulation. Understanding the mechanisms of how epigenetic regulators contribute to abnormal cell cycle regulation and ciliogenesis defects would lead to developing therapeutic strategies for the treatment of a wide variety of diseases, such as cancers, polycystic kidney disease (PKD), and other ciliopathy-associated disorders.

摘要

原发性纤毛生物发生与细胞周期进程密切相关。当细胞退出细胞周期并在有丝分裂后期进入静止阶段时,纤毛组装,并且在细胞重新进入新的细胞周期之前,纤毛会解体。研究集中在细胞周期如何与纤毛组装/拆卸过程协调,以及纤毛生物发生是否以及如何影响细胞周期。适当调节纤毛和细胞周期相关蛋白的功能和/或表达对于维持身体内稳态至关重要。表观遗传机制,包括 DNA 甲基化和组蛋白/染色质修饰,参与细胞周期进程和纤毛生物发生的调节。在这篇综述中,首先,我们讨论了表观遗传机制如何通过调节 DNA 甲基化和染色质结构来调节细胞周期进程和纤毛生物发生,从而促进或抑制与这些过程相关的基因的转录以及细胞骨架网络(包括微管和肌动蛋白)的修饰。接下来,我们讨论了细胞周期和纤毛发生之间的串扰,以及表观遗传调节剂在这个过程中的参与。此外,我们还讨论了纤毛依赖性信号通路在细胞周期调控中的作用。了解表观遗传调节剂如何有助于异常细胞周期调控和纤毛发生缺陷的机制,将为治疗各种疾病(如癌症、多囊肾病 (PKD) 和其他纤毛病相关疾病)的治疗方法的发展提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa57/8307023/618535e15620/cells-10-01662-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa57/8307023/019279fafd77/cells-10-01662-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa57/8307023/7256885425b7/cells-10-01662-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa57/8307023/618535e15620/cells-10-01662-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa57/8307023/019279fafd77/cells-10-01662-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa57/8307023/7256885425b7/cells-10-01662-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa57/8307023/618535e15620/cells-10-01662-g003.jpg

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