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FANCC在神经突生长过程中与UNC5A共定位,并促进神经突形成。

FANCC localizes with UNC5A at neurite outgrowth and promotes neuritogenesis.

作者信息

Huang FengFei, Ben Aissa Manel, Lévesque Georges, Carreau Madeleine

机构信息

Centre Hospitalier Universitaire de Québec-Université Laval, CHUL, 2705 Boul. Laurier, RC-9800, Quebec, QC, G1V 4G2, Canada.

Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Chicago, IL, USA.

出版信息

BMC Res Notes. 2018 Sep 12;11(1):662. doi: 10.1186/s13104-018-3763-1.

DOI:10.1186/s13104-018-3763-1
PMID:30213274
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6136181/
Abstract

OBJECTIVE

The Uncoordinated 5A (UNC5A) protein is part of a family of receptors that play roles in axonal pathfinding and cell migration. We previously showed that the Fanconi anemia C protein (FANCC) interacts with UNC5A and delays UNC5A-mediated apoptosis. FANCC is a predominantly cytoplasmic protein that has multiple functions including DNA damage signaling, oxygen radical metabolism, signal transduction, transcriptional regulation and apoptosis. Given the direct interaction between FANCC and UNC5A and that FANCC interferes with UNC5A-mediated apoptosis, we explored the possibility that FANCC might play a role in axonal-like growth processes.

RESULTS

Here we show that FANCC and UNC5A are localized to regions of neurite outgrowth during neuronal cell differentiation. We also show that absence of FANCC is required for neurite outgrowth. In addition, FANCC seems required for UNC5A expression. Results from this study combined with our previous report suggest that FANCC plays a role in tissue development through the regulation of UNC5A-mediated functions.

摘要

目的

不协调5A(UNC5A)蛋白是受体家族的一部分,在轴突导向和细胞迁移中发挥作用。我们之前表明,范可尼贫血C蛋白(FANCC)与UNC5A相互作用,并延迟UNC5A介导的细胞凋亡。FANCC是一种主要位于细胞质的蛋白,具有多种功能,包括DNA损伤信号传导、氧自由基代谢、信号转导、转录调控和细胞凋亡。鉴于FANCC与UNC5A之间的直接相互作用以及FANCC干扰UNC5A介导的细胞凋亡,我们探讨了FANCC可能在轴突样生长过程中发挥作用的可能性。

结果

在此我们表明,在神经元细胞分化过程中,FANCC和UNC5A定位于神经突生长区域。我们还表明,神经突生长需要缺失FANCC。此外,FANCC似乎是UNC5A表达所必需的。本研究结果与我们之前的报告相结合表明,FANCC通过调节UNC5A介导的功能在组织发育中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eab/6136181/323e834ecfcd/13104_2018_3763_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eab/6136181/4834fa87f19a/13104_2018_3763_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eab/6136181/2cf6dfe2870f/13104_2018_3763_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eab/6136181/323e834ecfcd/13104_2018_3763_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eab/6136181/4834fa87f19a/13104_2018_3763_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eab/6136181/2cf6dfe2870f/13104_2018_3763_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eab/6136181/323e834ecfcd/13104_2018_3763_Fig3_HTML.jpg

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2
Classical inherited bone marrow failure syndromes with high risk for myelodysplastic syndrome and acute myelogenous leukemia.具有骨髓增生异常综合征和急性髓系白血病高风险的经典遗传性骨髓衰竭综合征。
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Knowledge-driven binning approach for rare variant association analysis: application to neuroimaging biomarkers in Alzheimer's disease.
用于罕见变异关联分析的知识驱动分箱方法:在阿尔茨海默病神经影像生物标志物中的应用
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Fanconi anemia: correlating central nervous system malformations and genetic complementation groups.范可尼贫血:中枢神经系统畸形与基因互补组的关联
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An Alzheimer Disease-linked Rare Mutation Potentiates Netrin Receptor Uncoordinated-5C-induced Signaling That Merges with Amyloid β Precursor Protein Signaling.一种与阿尔茨海默病相关的罕见突变增强了与淀粉样前体蛋白信号传导合并的网蛋白受体Uncoordinated-5C诱导的信号传导。
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Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imaging.范可尼贫血患者的中枢神经系统异常:磁共振成像的表现形式及发生率
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