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Dclk1基因可变剪接变体的表达受精神药物调控。

Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs.

作者信息

Zygmunt Magdalena, Hoinkis Dżesika, Hajto Jacek, Piechota Marcin, Skupień-Rabian Bożena, Jankowska Urszula, Kędracka-Krok Sylwia, Rodriguez Parkitna Jan, Korostyński Michał

机构信息

Department of Molecular Neuropharmacology, Institute of Pharmacology of the Polish Academy of Sciences, Smetna 12, 31-343, Krakow, Poland.

Laboratory of Proteomics and Mass Spectrometry, Malopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland.

出版信息

BMC Neurosci. 2018 Sep 12;19(1):55. doi: 10.1186/s12868-018-0458-4.

Abstract

BACKGROUND

The long-term effects of psychotropic drugs are associated with the reversal of disease-related alterations through the reorganization and normalization of neuronal connections. Molecular factors that trigger drug-induced brain plasticity remain only partly understood. Doublecortin-like kinase 1 (Dclk1) possesses microtubule-polymerizing activity during synaptic plasticity and neurogenesis. However, the Dclk1 gene shows a complex profile of transcriptional regulation, with two alternative promoters and exon splicing patterns that suggest the expression of multiple isoforms with different kinase activities.

RESULTS

Here, we applied next-generation sequencing to analyze changes in the expression of Dclk1 gene isoforms in the brain in response to several psychoactive drugs with diverse pharmacological mechanisms of action. We used bioinformatics tools to define the range and levels of Dclk1 transcriptional regulation in the mouse nucleus accumbens and prefrontal cortex. We also sought to investigate the presence of DCLK1-derived peptides using mass spectrometry. We detected 15 transcripts expressed from the Dclk1 locus (FPKM > 1), including 2 drug-regulated variants (fold change > 2). Drugs that act on serotonin receptors (5-HT2A/C) regulate a subset of Dclk1 isoforms in a brain-region-specific manner. The strongest influence was observed for the mianserin-induced expression of an isoform with intron retention. The drug-activated expression of novel alternative Dclk1 isoforms was validated using qPCR. The drug-regulated isoform contains genetic variants of DCLK1 that have been previously associated with schizophrenia and hyperactivity disorder in humans. We identified a short peptide that might originate from the novel DCLK1 protein product. Moreover, protein domains encoded by the regulated variant indicate their potential involvement in the negative regulation of the canonical DCLK1 protein.

CONCLUSIONS

In summary, we identified novel isoforms of the neuroplasticity-related gene Dclk1 that are expressed in the brain in response to psychotropic drug treatments.

摘要

背景

精神药物的长期作用与通过神经元连接的重组和正常化来逆转疾病相关改变有关。触发药物诱导的脑可塑性的分子因素仍仅部分为人所知。双皮质素样激酶1(Dclk1)在突触可塑性和神经发生过程中具有微管聚合活性。然而,Dclk1基因显示出复杂的转录调控图谱,有两个可变启动子和外显子剪接模式,这表明存在具有不同激酶活性的多种异构体表达。

结果

在此,我们应用下一代测序技术来分析大脑中Dclk1基因异构体的表达变化,以响应几种具有不同药理作用机制的精神活性药物。我们使用生物信息学工具来确定小鼠伏隔核和前额叶皮质中Dclk1转录调控的范围和水平。我们还试图使用质谱法研究DCLK1衍生肽的存在。我们检测到从Dclk1位点表达的15种转录本(FPKM>1),包括2种药物调节变体(倍数变化>2)。作用于5-羟色胺受体(5-HT2A/C)的药物以脑区特异性方式调节Dclk1异构体的一个子集。观察到米安色林诱导的内含子保留异构体表达的影响最强。使用qPCR验证了新型可变Dclk1异构体的药物激活表达。药物调节的异构体包含先前与人类精神分裂症和多动障碍相关的DCLK1基因变体。我们鉴定出一种可能源自新型DCLK1蛋白产物的短肽。此外,受调节变体编码的蛋白结构域表明它们可能参与了经典DCLK1蛋白的负调控。

结论

总之,我们鉴定出了与神经可塑性相关的基因Dclk1的新型异构体,它们在大脑中因精神药物治疗而表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7869/6134793/17831f578757/12868_2018_458_Fig1_HTML.jpg

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