Suppr超能文献

多聚谷氨酰胺(polyQ)疾病:染色质的联系。

Polyglutamine (polyQ) disorders: the chromatin connection.

机构信息

Department of Genetics, The Institute of Life Sciences, The Hebrew University of Jerusalem-Edmond J. Safra Campus, Jerusalem, Israel.

出版信息

Nucleus. 2012 Sep-Oct;3(5):433-41. doi: 10.4161/nucl.21481. Epub 2012 Aug 15.

Abstract

Polyglutamine (PolyQ)-related diseases are dominant late-onset genetic disorders that are manifested by progressive neurodegeneration, leading to behavioral and physical impairments. An increased body of evidence suggests that chromatin structure and epigenetic regulation are involved in disease pathology. PolyQ diseases often display an aberrant transcriptional regulation due to the disrupted function of histone-modifying complexes and altered interactions of the polyQ-extended proteins with chromatin-related factors. In this review we describe recent findings relating to the role of chromatin in polyQ diseases. We discuss the involvement of epigenetic-related factors and chromatin structure in genomic instability of CAG repeats; we describe changes in the expression and regulation of chromatin-related enzymes and in the levels and patterns of histone modifications in disease state; we illustrate the potential beneficial effects of different histone deacetylase (HDAC) inhibitors for the treatment of polyQ diseases, and we end by describing the potential use of human pluripotent stem cells and their differentiated derivatives for modeling polyQ diseases in vitro. Taken together, these accumulating studies strongly suggest that disrupted chromatin regulation may be directly involved with the pathophysiology of polyQ-related diseases.

摘要

多聚谷氨酰胺(PolyQ)相关性疾病是显性迟发性遗传疾病,表现为进行性神经退行性变,导致行为和身体功能障碍。越来越多的证据表明,染色质结构和表观遗传调控参与了疾病的发病机制。由于组蛋白修饰复合物功能紊乱以及多聚谷氨酰胺延伸蛋白与染色质相关因子的相互作用改变,PolyQ 疾病通常表现出异常的转录调控。在这篇综述中,我们描述了与染色质在 PolyQ 疾病中的作用相关的最新发现。我们讨论了与表观遗传相关的因素和染色质结构在 CAG 重复不稳定中的作用;我们描述了染色质相关酶的表达和调节以及疾病状态下组蛋白修饰水平和模式的变化;我们说明了不同组蛋白去乙酰化酶(HDAC)抑制剂在治疗 PolyQ 疾病方面的潜在有益作用,并最后描述了人类多能干细胞及其分化衍生物在体外模拟 PolyQ 疾病的潜在用途。综上所述,这些不断积累的研究强烈表明,染色质调控的破坏可能直接参与 PolyQ 相关疾病的病理生理学。

相似文献

1
Polyglutamine (polyQ) disorders: the chromatin connection.
Nucleus. 2012 Sep-Oct;3(5):433-41. doi: 10.4161/nucl.21481. Epub 2012 Aug 15.
2
[Histone deacetylase inhibitors as therapeutic agents for polyglutamine disorders].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Feb;27(1):52-5. doi: 10.3760/cma.j.issn.1003-9406.2010.01.011.
3
Gene Alterations Induced by Glutamine (Q) Encoding CAG Repeats Associated with Neurodegeneration.
Methods Mol Biol. 2023;2575:3-23. doi: 10.1007/978-1-0716-2716-7_1.
5
Deregulation of histone-modifying enzymes and chromatin structure modifiers contributes to glioma development.
Future Oncol. 2015 Sep;11(18):2587-601. doi: 10.2217/fon.15.171. Epub 2015 Aug 20.
7
Epigenetic profiles in polyglutamine disorders.
Epigenomics. 2018 Jan;10(1):9-25. doi: 10.2217/epi-2017-0089. Epub 2017 Nov 27.
9
Histone deacetylase inhibitors as therapeutics for polyglutamine disorders.
Nat Rev Neurosci. 2006 Oct;7(10):784-96. doi: 10.1038/nrn1989.

引用本文的文献

1
Developmental and physiological impacts of pathogenic human huntingtin protein in the nervous system.
Neurobiol Dis. 2024 Dec;203:106732. doi: 10.1016/j.nbd.2024.106732. Epub 2024 Nov 12.
2
Polyglutamine (PolyQ) Diseases: Navigating the Landscape of Neurodegeneration.
ACS Chem Neurosci. 2024 Aug 7;15(15):2665-2694. doi: 10.1021/acschemneuro.4c00184. Epub 2024 Jul 12.
3
Neuroprotective effects of flavonoids: endoplasmic reticulum as the target.
Front Neurosci. 2024 Jun 18;18:1348151. doi: 10.3389/fnins.2024.1348151. eCollection 2024.
5
What the Gut Tells the Brain-Is There a Link between Microbiota and Huntington's Disease?
Int J Mol Sci. 2023 Feb 24;24(5):4477. doi: 10.3390/ijms24054477.
6
as a model system for studying aging-associated neurodegenerative diseases.
Transl Med Aging. 2020;4:60-72. doi: 10.1016/j.tma.2020.05.001. Epub 2020 Jun 10.
7
Fic and non-Fic AMPylases: protein AMPylation in metazoans.
Open Biol. 2021 May;11(5):210009. doi: 10.1098/rsob.210009. Epub 2021 May 5.
8
Open chromatin structure in PolyQ disease-related genes: a potential mechanism for CAG repeat expansion in the normal human population.
NAR Genom Bioinform. 2019 Jul 30;1(1):e3. doi: 10.1093/nargab/lqz003. eCollection 2019 Apr.
9
Epigenetic mechanisms of neurodegenerative diseases and acute brain injury.
Neurochem Int. 2020 Feb;133:104642. doi: 10.1016/j.neuint.2019.104642. Epub 2019 Dec 12.
10
Hat1 acetylates histone H4 and modulates the transcriptional program in Drosophila embryogenesis.
Sci Rep. 2019 Nov 29;9(1):17973. doi: 10.1038/s41598-019-54497-0.

本文引用的文献

6
Standardized generation and differentiation of neural precursor cells from human pluripotent stem cells.
Stem Cell Rev Rep. 2013 Aug;9(4):531-6. doi: 10.1007/s12015-012-9357-8.
7
Histone deacetylase complexes promote trinucleotide repeat expansions.
PLoS Biol. 2012 Feb;10(2):e1001257. doi: 10.1371/journal.pbio.1001257. Epub 2012 Feb 21.
8
Genetic knock-down of HDAC3 does not modify disease-related phenotypes in a mouse model of Huntington's disease.
PLoS One. 2012;7(2):e31080. doi: 10.1371/journal.pone.0031080. Epub 2012 Feb 8.
9
Intracerebral transplantation for neurological disorders. Lessons from developmental, experimental, and clinical studies.
Front Cell Neurosci. 2012 Jan 27;6:2. doi: 10.3389/fncel.2012.00002. eCollection 2011 Jan.
10
DNA base excision repair: a mechanism of trinucleotide repeat expansion.
Trends Biochem Sci. 2012 Apr;37(4):162-72. doi: 10.1016/j.tibs.2011.12.002. Epub 2012 Jan 27.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验