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17β-estradiol regulates the RNA-binding protein Nova1, which then regulates the alternative splicing of estrogen receptor β in the aging female rat brain.17β-雌二醇调节 RNA 结合蛋白 Nova1,进而调节衰老雌性大鼠大脑中雌激素受体β的可变剪接。
Neurobiol Aging. 2018 Jan;61:13-22. doi: 10.1016/j.neurobiolaging.2017.09.005. Epub 2017 Sep 14.
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本文引用的文献

1
Integrative modeling defines the Nova splicing-regulatory network and its combinatorial controls.综合建模定义了 Nova 剪接调控网络及其组合控制。
Science. 2010 Jul 23;329(5990):439-43. doi: 10.1126/science.1191150. Epub 2010 Jun 17.
2
Histochemical mapping of hnRNP A2/B1 in rat brain after ischemia-reperfusion insults.缺血再灌注损伤后大鼠脑内 hnRNP A2/B1 的组织化学定位。
J Histochem Cytochem. 2010 Aug;58(8):695-705. doi: 10.1369/jhc.2010.955021. Epub 2010 Apr 26.
3
The Neuronal Splicing Factor Nova Co-Localizes with Target RNAs in the Dendrite.神经元剪接因子 Nova 与树突中的靶 RNA 共定位。
Front Neural Circuits. 2010 Mar 3;4:5. doi: 10.3389/neuro.04.005.2010. eCollection 2010.
4
Antidepressive behaviors induced byenriched environment might be modulated by glucocorticoid levels.丰富环境诱导的抗抑郁行为可能受糖皮质激素水平的调节。
Eur Neuropsychopharmacol. 2009 Dec;19(12):868-75. doi: 10.1016/j.euroneuro.2009.07.004. Epub 2009 Aug 6.
5
Transcription and splicing regulation in human umbilical vein endothelial cells under hypoxic stress conditions by exon array.外显子芯片研究缺氧应激条件下人脐静脉内皮细胞的转录和剪接调控
BMC Genomics. 2009 Mar 25;10:126. doi: 10.1186/1471-2164-10-126.
6
HITS-CLIP yields genome-wide insights into brain alternative RNA processing.HITS-CLIP技术使人们能够在全基因组范围内深入了解大脑中的可变RNA加工过程。
Nature. 2008 Nov 27;456(7221):464-9. doi: 10.1038/nature07488. Epub 2008 Nov 2.
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Alternative splicing in cancer: noise, functional, or systematic?癌症中的可变剪接:是噪音、功能性的还是系统性的?
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8
Alternative splicing: an emerging topic in molecular and clinical oncology.可变剪接:分子与临床肿瘤学中的一个新兴话题。
Lancet Oncol. 2007 Apr;8(4):349-57. doi: 10.1016/S1470-2045(07)70104-3.
9
An RNA map predicting Nova-dependent splicing regulation.一张预测Nova依赖的剪接调控的RNA图谱。
Nature. 2006 Nov 30;444(7119):580-6. doi: 10.1038/nature05304. Epub 2006 Oct 25.
10
Alternative splicing: new insights from global analyses.可变剪接:全局分析带来的新见解
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局灶性脑缺血/再灌注损伤后大鼠脑内神经肿瘤学腹侧抗原 1(Nova1)的动态表达模式。

Dynamic expression pattern of neuro-oncological ventral antigen 1 (Nova1) in the rat brain after focal cerebral ischemia/reperfusion insults.

机构信息

Beijing Institute of Radiation Medicine, State Key Laboratory of Proteomics, State Key Laboratory of Medical Neurobiology, Cognitive and Mental Health Research Center, Beijing, China.

出版信息

J Histochem Cytochem. 2013 Jan;61(1):45-54. doi: 10.1369/0022155412461255. Epub 2012 Oct 5.

DOI:10.1369/0022155412461255
PMID:23042482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3534313/
Abstract

The present study aimed to evaluate the expression of neuro-oncological ventral antigen 1 (Nova1) in cerebral ischemia/reperfusion (I/R) insults by immunohistochemistry. The focal cerebral I/R model was induced by right middle cerebral artery occlusion (MCAO) for 120 min followed by 1 day, 7 days, and 14 days of reperfusion in Sprague-Dawley (SD) rats. The results showed that Nova1 was expressed in nearly the whole brain, although with higher density in hippocampus, hypothalamus, cingulate cortex, and medial habenular nucleus. The immunoreactivity of Nova1 neurons was increased dramatically, especially on both sides of the hippocampal CA(1) region, after 1 day of reperfusion. A strong response occurred at the ipsilateral CA(1) region between 1 day and 7 days of reperfusion. Likewise, strong compensatory responses of Nova1 expression were observed on the contralateral side of the striate cortex, dentate gyrus, and hypothalamus. Interestingly, more Nova1 neurons were observed to translocate to the dendrites and growth cones of the axons in the hypothalamus on the ischemic side after 7 days of reperfusion. In conclusion, our data suggest that Nova1 might mediate neuronal responsiveness, and its expression might positively correlate with neural repair after I/R insults in the rat brain.

摘要

本研究旨在通过免疫组织化学方法评估神经肿瘤学腹侧抗原 1(Nova1)在脑缺血/再灌注(I/R)损伤中的表达。采用右侧大脑中动脉闭塞(MCAO)法诱导 Sprague-Dawley(SD)大鼠局灶性脑 I/R 模型,再灌注 1 天、7 天和 14 天。结果表明,Nova1 在全脑中均有表达,但在海马、下丘脑、扣带回和内侧缰核中表达密度更高。Nova1 神经元的免疫反应性在再灌注 1 天后显著增强,尤其是在海马 CA(1)区的两侧。在再灌注 1 天至 7 天期间,同侧 CA(1)区出现强烈反应。同样,纹状体皮层、齿状回和下丘脑对侧也观察到 Nova1 表达的强烈代偿反应。有趣的是,再灌注 7 天后,缺血侧下丘脑的 Nova1 神经元更多地迁移到轴突的树突和生长锥中。总之,我们的数据表明,Nova1 可能介导神经元反应性,其表达可能与大鼠脑 I/R 损伤后的神经修复呈正相关。