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本文引用的文献

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Targeted degradation of aberrant tau in frontotemporal dementia patient-derived neuronal cell models.靶向降解额颞叶痴呆患者来源神经元细胞模型中的异常 tau。
Elife. 2019 Mar 25;8:e45457. doi: 10.7554/eLife.45457.
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Antisense oligonucleotide-mediated ataxin-1 reduction prolongs survival in SCA1 mice and reveals disease-associated transcriptome profiles.反义寡核苷酸介导的 ataxin-1 减少可延长 SCA1 小鼠的存活时间,并揭示与疾病相关的转录组特征。
JCI Insight. 2018 Nov 2;3(21):123193. doi: 10.1172/jci.insight.123193.
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TPMCalculator: one-step software to quantify mRNA abundance of genomic features.TPMCalculator:一步式软件,可定量基因组特征的 mRNA 丰度。
Bioinformatics. 2019 Jun 1;35(11):1960-1962. doi: 10.1093/bioinformatics/bty896.
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Selective vulnerability in neurodegenerative diseases.神经退行性疾病中的选择性脆弱性。
Nat Neurosci. 2018 Oct;21(10):1350-1358. doi: 10.1038/s41593-018-0221-2. Epub 2018 Sep 24.
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A Druggable Genome Screen Identifies Modifiers of α-Synuclein Levels via a Tiered Cross-Species Validation Approach.药物基因组筛选通过分层跨物种验证方法鉴定α-突触核蛋白水平的调节剂。
J Neurosci. 2018 Oct 24;38(43):9286-9301. doi: 10.1523/JNEUROSCI.0254-18.2018. Epub 2018 Sep 24.
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Loss of from neurons regulating hypoxic and hypercapnic chemoresponses causes neonatal respiratory failure in mice.神经元中调节低氧和高碳酸血症化学感受反应的缺失导致小鼠新生儿呼吸衰竭。
Elife. 2018 Jul 4;7:e38455. doi: 10.7554/eLife.38455.
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SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium.SPATA7 在远端连接纤毛中维持一个新型的光感受器特异性区域。
J Cell Biol. 2018 Aug 6;217(8):2851-2865. doi: 10.1083/jcb.201712117. Epub 2018 Jun 13.
8
PAK1 regulates ATXN1 levels providing an opportunity to modify its toxicity in spinocerebellar ataxia type 1.PAK1 调节 ATXN1 水平,为修饰 1 型脊髓小脑共济失调的毒性提供了机会。
Hum Mol Genet. 2018 Aug 15;27(16):2863-2873. doi: 10.1093/hmg/ddy200.
9
ATXN1-CIC Complex Is the Primary Driver of Cerebellar Pathology in Spinocerebellar Ataxia Type 1 through a Gain-of-Function Mechanism.ATXN1-CIC 复合物通过获得性功能机制成为脊髓小脑共济失调 1 型小脑病理学的主要驱动因素。
Neuron. 2018 Mar 21;97(6):1235-1243.e5. doi: 10.1016/j.neuron.2018.02.013. Epub 2018 Mar 8.
10
Motor neuron degeneration correlates with respiratory dysfunction in SCA1.运动神经元退化与 SCA1 的呼吸功能障碍相关。
Dis Model Mech. 2018 Feb 26;11(2):dmm032623. doi: 10.1242/dmm.032623.

双重靶向脑区特异性激酶增强脊髓小脑共济失调 1 型的神经保护作用。

Dual targeting of brain region-specific kinases potentiates neurological rescue in Spinocerebellar ataxia type 1.

机构信息

Integrative Molecular and Biomedical Science Program, Baylor College of Medicine, Houston, TX, USA.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

出版信息

EMBO J. 2021 Apr 1;40(7):e106106. doi: 10.15252/embj.2020106106. Epub 2021 Mar 11.

DOI:10.15252/embj.2020106106
PMID:33709453
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8013850/
Abstract

A critical question in neurodegeneration is why the accumulation of disease-driving proteins causes selective neuronal loss despite their brain-wide expression. In Spinocerebellar ataxia type 1 (SCA1), accumulation of polyglutamine-expanded Ataxin-1 (ATXN1) causes selective degeneration of cerebellar and brainstem neurons. Previous studies revealed that inhibiting Msk1 reduces phosphorylation of ATXN1 at S776 as well as its levels leading to improved cerebellar function. However, there are no regulators that modulate ATXN1 in the brainstem-the brain region whose pathology is most closely linked to premature death. To identify new regulators of ATXN1, we performed genetic screens and identified a transcription factor-kinase axis (ZBTB7B-RSK3) that regulates ATXN1 levels. Unlike MSK1, RSK3 is highly expressed in the human and mouse brainstems where it regulates Atxn1 by phosphorylating S776. Reducing Rsk3 rescues brainstem-associated pathologies and deficits, and lowering Rsk3 and Msk1 together improves cerebellar and brainstem function in an SCA1 mouse model. Our results demonstrate that selective vulnerability of brain regions in SCA1 is governed by region-specific regulators of ATXN1, and targeting multiple regulators could rescue multiple degenerating brain areas.

摘要

神经退行性疾病的一个关键问题是,为什么尽管疾病驱动蛋白在大脑中广泛表达,但它们的积累会导致选择性神经元丧失。在脊髓小脑共济失调 1 型(SCA1)中,聚谷氨酰胺扩展的 Ataxin-1(ATXN1)的积累导致小脑和脑干神经元的选择性退化。先前的研究表明,抑制 Msk1 可减少 ATXN1 在 S776 处的磷酸化及其水平,从而改善小脑功能。然而,在与过早死亡最密切相关的脑区——脑干中,没有调节 ATXN1 的调节剂。为了鉴定 ATXN1 的新调节剂,我们进行了遗传筛选,并鉴定出一个转录因子-激酶轴(ZBTB7B-RSK3),它调节 ATXN1 的水平。与 MSK1 不同,RSK3 在人和小鼠脑干中高度表达,通过磷酸化 S776 来调节 Atxn1。降低 Rsk3 可挽救与脑干相关的病理和缺陷,并且降低 Rsk3 和 Msk1 可共同改善 SCA1 小鼠模型中的小脑和脑干功能。我们的结果表明,SCA1 中脑区的选择性脆弱性受 ATXN1 的区域特异性调节剂控制,靶向多个调节剂可以挽救多个退化的脑区。