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本文引用的文献

1
Rhes, a striatal-enriched protein, promotes mitophagy via Nix.Rhes,一种纹状体丰富的蛋白,通过 Nix 促进线粒体自噬。
Proc Natl Acad Sci U S A. 2019 Nov 19;116(47):23760-23771. doi: 10.1073/pnas.1912868116. Epub 2019 Nov 1.
2
Conformation Polymorphism of Polyglutamine Proteins.多聚谷氨酰胺蛋白的构象多态性。
Trends Biochem Sci. 2018 Jun;43(6):424-435. doi: 10.1016/j.tibs.2018.03.002. Epub 2018 Apr 7.
3
Sphingomyelin and GM1 Influence Huntingtin Binding to, Disruption of, and Aggregation on Lipid Membranes.鞘磷脂和GM1影响亨廷顿蛋白与脂质膜的结合、对脂质膜的破坏以及在脂质膜上的聚集。
ACS Omega. 2018 Jan 31;3(1):273-285. doi: 10.1021/acsomega.7b01472. Epub 2018 Jan 10.
4
CRISPR/Cas9-mediated gene editing ameliorates neurotoxicity in mouse model of Huntington's disease.CRISPR/Cas9介导的基因编辑改善了亨廷顿舞蹈病小鼠模型中的神经毒性。
J Clin Invest. 2017 Jun 30;127(7):2719-2724. doi: 10.1172/JCI92087. Epub 2017 Jun 19.
5
Huntingtin-associated protein-1 (HAP1) regulates endocytosis and interacts with multiple trafficking-related proteins.亨廷顿蛋白相关蛋白1(HAP1)调节内吞作用,并与多种运输相关蛋白相互作用。
Cell Signal. 2017 Jul;35:176-187. doi: 10.1016/j.cellsig.2017.02.023. Epub 2017 Mar 1.
6
Immunohistochemical analysis of huntingtin-associated protein 1 in adult rat spinal cord and its regional relationship with androgen receptor.成年大鼠脊髓中亨廷顿相关蛋白1的免疫组织化学分析及其与雄激素受体的区域关系。
Neuroscience. 2017 Jan 6;340:201-217. doi: 10.1016/j.neuroscience.2016.10.053. Epub 2016 Oct 29.
7
Acetylation within the First 17 Residues of Huntingtin Exon 1 Alters Aggregation and Lipid Binding.亨廷顿蛋白外显子1前17个残基内的乙酰化改变聚集和脂质结合。
Biophys J. 2016 Jul 26;111(2):349-362. doi: 10.1016/j.bpj.2016.06.018.
8
Huntington disease.亨廷顿舞蹈病。
Nat Rev Dis Primers. 2015 Apr 23;1:15005. doi: 10.1038/nrdp.2015.5.
9
The Biology of Huntingtin.亨廷顿蛋白的生物学。
Neuron. 2016 Mar 2;89(5):910-26. doi: 10.1016/j.neuron.2016.02.003.
10
Downregulation of GABA Receptor Recycling Mediated by HAP1 Contributes to Neuronal Death in In Vitro Brain Ischemia.由HAP1介导的GABA受体再循环的下调促成体外脑缺血中的神经元死亡。
Mol Neurobiol. 2017 Jan;54(1):45-57. doi: 10.1007/s12035-015-9661-9. Epub 2016 Jan 5.

Hap1 缺失选择性促进亨廷顿病小鼠纹状体变性。

Loss of Hap1 selectively promotes striatal degeneration in Huntington disease mice.

机构信息

Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322.

出版信息

Proc Natl Acad Sci U S A. 2020 Aug 18;117(33):20265-20273. doi: 10.1073/pnas.2002283117. Epub 2020 Aug 3.

DOI:10.1073/pnas.2002283117
PMID:32747555
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7443904/
Abstract

Huntington disease (HD) is an ideal model for investigating selective neurodegeneration, as expanded polyQ repeats in the ubiquitously expressed huntingtin (HTT) cause the preferential neurodegeneration in the striatum of the HD patient brains. Here we report that adeno-associated virus (AAV) transduction-mediated depletion of Hap1, the first identified huntingtin-associated protein, in adult HD knock-in (KI) mouse brains leads to selective neuronal loss in the striatum. Further, Hap1 depletion-mediated neuronal loss via AAV transduction requires the presence of mutant HTT. Rhes, a GTPase that is enriched in the striatum and sumoylates mutant HTT to mediate neurotoxicity, binds more N-terminal HTT when Hap1 is deficient. Consistently, more soluble and sumoylated N-terminal HTT is presented in HD KI mouse striatum when HAP1 is absent. Our findings suggest that both Rhes and Hap1 as well as cellular stress contribute to the preferential neurodegeneration in HD, highlighting the involvement of multiple factors in selective neurodegeneration.

摘要

亨廷顿病(HD)是研究选择性神经退行性变的理想模型,因为在广泛表达的亨廷顿蛋白(HTT)中扩展的 polyQ 重复导致 HD 患者大脑纹状体中的选择性神经退行性变。在这里,我们报告说,腺相关病毒(AAV)转导介导的成年 HD 基因敲入(KI)小鼠大脑中第一个被鉴定的亨廷顿蛋白相关蛋白 Hap1 的耗竭导致纹状体中选择性神经元丢失。此外,通过 AAV 转导的 Hap1 耗竭介导的神经元丢失需要存在突变型 HTT。Rhes 是一种富含纹状体并通过 SUMOylation 介导神经毒性的 GTPase,当 Hap1 缺乏时,它与更多的 N 端 HTT 结合。一致地,当 HAP1 不存在时,HD KI 小鼠纹状体中存在更多的可溶性和 SUMOylated N 端 HTT。我们的发现表明,Rhes 和 Hap1 以及细胞应激都有助于 HD 中的选择性神经退行性变,突出了多种因素在选择性神经退行性变中的参与。