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

LCN-2 PCBP1 Parkinson’s disease WWP-2 alternative splicing

Journal

Frontiers in aging neuroscience
ISSN: 1663-4365
Titre abrégé: Front Aging Neurosci
Pays: Switzerland
ID NLM: 101525824

Informations de publication

Date de publication:
2022
Historique:
received: 27 02 2022
accepted: 25 05 2022
entrez: 7 7 2022
pubmed: 8 7 2022
medline: 8 7 2022
Statut: epublish

Résumé

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

Identifiants

pubmed: 35795237
doi: 10.3389/fnagi.2022.884837
pmc: PMC9251440
doi:

Types de publication

Journal Article

Langues

eng

Pagination

884837

Informations de copyright

Copyright © 2022 Yusufujiang, Zeng, Yang, Jing, Yang and Li.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Aishanjiang Yusufujiang (A)

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.

Shan Zeng (S)

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.

Chen Yang (C)

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.

Sha Jing (S)

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.

Lijuan Yang (L)

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.

Hongyan Li (H)

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.

Classifications MeSH