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PCBP-1调节PC12细胞中炎症和泛素化相关基因的转录及可变剪接。

PCBP-1 Regulates the Transcription and Alternative Splicing of Inflammation and Ubiquitination-Related Genes in PC12 Cell.

作者信息

Yusufujiang Aishanjiang, Zeng Shan, Yang Chen, Jing Sha, Yang Lijuan, Li Hongyan

机构信息

Department of Neurology, People's Hospital of Xinjiang Uygur Autonomous Region, Ürümqi, China.

Xinjiang Clinical Research Center for Stroke and Neurological Rare Disease, Ürümqi, China.

出版信息

Front Aging Neurosci. 2022 Jun 20;14:884837. doi: 10.3389/fnagi.2022.884837. eCollection 2022.

Abstract

PCBP-1, a multifunctional RNA binding protein, is expressed in various human cell/tissue types and involved in post-transcriptional gene regulation. PCBP-1 has important roles in cellular Iron homeostasis, mitochondrial stability, and other cellular activities involved in the pathophysiological process of neurodegenerative diseases, such as amyotrophic lateral sclerosis (ALS) and Huntington's disease (HD). However, it remains enigmatic whether PCPB-1 is associated with the pathogenesis of PD. In this study, we cloned and constitutively overexpressed PCBP-1 in rat PC12 cells (PC12 cell is the common cell line studying neurodegenerative disease include PD). RNA-seq was performed to analyze PCBP-1-regulated differentially expressed genes (DEGs) and alternative splicing events (ASEs) between control and PCBP1-overexpressed cells. GO and KEGG pathway analyses were performed to identify functional DEGs and alternatively spliced genes. Consequently, we validated PCBP-1-regulated genes using RT-qPCR. Finally, we downloaded CLIP-seq data from GEO (GSE84700) to analyze the mechanisms of PCBP-1's regulation of gene expression and ASEs by revealing the binding profile of PCBP-1 on its target pre-mRNAs. Overexpression of PCBP-1 partially regulated the ASE and expression of genes enriched in neuroinflammation and protein ubiquitination, which were also associated with PD pathogenesis. Moreover, RT-qPCR assay verified the PCBP-1-modulated expression of neuroinflammatory genes, like , and alternative splicing (AS) of ubiquitination-related gene . Finally, CLIP-seq data analysis indicated that the first UC motif was the critical site for PCBP-1 binding to its targets. In this study, we provided evidence that PCBP-1 could regulate the expression of gene expression associated with neuroinflammation and AS of WWP-2 in relation to protein ubiquitination. These findings thus provided novel insights into the potential application of PCBP-1 as the disease pathophysiological or therapeutic target for neurodegenerative disease.

摘要

PCBP-1是一种多功能RNA结合蛋白,在多种人类细胞/组织类型中表达,并参与转录后基因调控。PCBP-1在细胞铁稳态、线粒体稳定性以及神经退行性疾病(如肌萎缩侧索硬化症(ALS)和亨廷顿舞蹈病(HD))病理生理过程中涉及的其他细胞活动中发挥重要作用。然而,PCPB-1是否与帕金森病(PD)的发病机制相关仍不清楚。在本研究中,我们在大鼠PC12细胞(PC12细胞是研究包括PD在内的神经退行性疾病的常用细胞系)中克隆并组成性过表达PCBP-1。进行RNA测序以分析对照细胞和PCBP1过表达细胞之间PCBP-1调节的差异表达基因(DEG)和可变剪接事件(ASE)。进行基因本体(GO)和京都基因与基因组百科全书(KEGG)通路分析以鉴定功能性DEG和可变剪接基因。因此,我们使用逆转录定量聚合酶链反应(RT-qPCR)验证了PCBP-1调节的基因。最后,我们从基因表达综合数据库(GEO,GSE84700)下载交联免疫沉淀测序(CLIP-seq)数据,通过揭示PCBP-1在其靶前体mRNA上的结合图谱来分析PCBP-1对基因表达和ASE的调控机制。PCBP-1的过表达部分调节了ASE以及在神经炎症和蛋白质泛素化中富集的基因的表达,这些也与PD发病机制相关。此外,RT-qPCR分析验证了PCBP-1对神经炎症基因(如 )的表达调节以及泛素化相关基因的可变剪接(AS)。最后,CLIP-seq数据分析表明第一个UC基序是PCBP-1与其靶标结合的关键位点。在本研究中,我们提供了证据表明PCBP-1可以调节与神经炎症相关的基因表达以及与蛋白质泛素化相关的WWP-2的AS。因此,这些发现为PCBP-1作为神经退行性疾病的疾病病理生理或治疗靶点的潜在应用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d3/9251440/f8b5fca30185/fnagi-14-884837-g001.jpg

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