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可卡因改变伏隔核中的 Homer1 自然反义转录本。

Cocaine alters Homer1 natural antisense transcript in the nucleus accumbens.

机构信息

Center for Therapeutic Innovation and Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of Medicine, Miami, FL 33136, United States.

Center for Therapeutic Innovation and Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of Medicine, Miami, FL 33136, United States.

出版信息

Mol Cell Neurosci. 2017 Dec;85:183-189. doi: 10.1016/j.mcn.2017.10.003. Epub 2017 Oct 18.

DOI:10.1016/j.mcn.2017.10.003
PMID:29055697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5698162/
Abstract

Natural antisense transcripts (NATs) are an abundant class of long noncoding RNAs that have recently been shown to be key regulators of chromatin dynamics and gene expression in nervous system development and neurological disorders. However, it is currently unclear if NAT-based mechanisms also play a role in drug-induced neuroadaptations. Aberrant regulation of gene expression is one critical factor underlying the long-lasting behavioral abnormalities that characterize substance use disorder, and it is possible that some drug-induced transcriptional responses are mediated, in part, by perturbations in NAT activity. To test this hypothesis, we used an automated algorithm that mines the NCBI AceView transcriptomics database to identify NAT overlapping genes linked to addiction. We found that 22% of the genes examined contain NATs and that expression of Homer1 natural antisense transcript (Homer1-AS) was altered in the nucleus accumbens (NAc) of mice 2h and 10days following repeated cocaine administration. In in vitro studies, depletion of Homer1-AS lead to an increase in the corresponding sense gene expression, indicating a potential regulatory mechanisms of Homer1 expression by its corresponding antisense transcript. Future in vivo studies are needed to definitely determine a role for Homer1-AS in cocaine-induced behavioral and molecular adaptations.

摘要

天然反义转录本 (NATs) 是一类丰富的长非编码 RNA,最近研究表明它们是神经系统发育和神经紊乱中染色质动态和基因表达的关键调节剂。然而,目前尚不清楚基于 NAT 的机制是否也在药物引起的神经适应中发挥作用。基因表达的异常调节是导致物质使用障碍特征性持久行为异常的一个关键因素,并且一些药物引起的转录反应可能部分受到 NAT 活性的干扰。为了验证这一假设,我们使用了一种自动算法,该算法挖掘 NCBI AceView 转录组学数据库,以鉴定与成瘾相关的 NAT 重叠基因。我们发现,在接受重复可卡因处理后的 2 小时和 10 天后,检测到的 22%的基因含有 NAT,并且 Homer1 天然反义转录本 (Homer1-AS) 在伏隔核 (NAc) 中的表达发生改变。在体外研究中,Homer1-AS 的耗竭导致相应有义基因表达增加,表明 Homer1 表达可能受到其相应反义转录本的调控。需要进行未来的体内研究,以确定 Homer1-AS 在可卡因引起的行为和分子适应中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/77fc47d392dc/nihms917213f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/0305942fc191/nihms917213f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/67ffe3c2b708/nihms917213f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/2ed821dac471/nihms917213f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/da5678c8efca/nihms917213f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/77fc47d392dc/nihms917213f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/0305942fc191/nihms917213f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/67ffe3c2b708/nihms917213f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/2ed821dac471/nihms917213f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/da5678c8efca/nihms917213f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/5698162/77fc47d392dc/nihms917213f5.jpg

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