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Exonic circular RNAs (ecircRNAs) in animal cells are generated by backsplicing, and the biogenesis of ecircRNAs is regulated by an array of RNA binding proteins (RBPs). HNRNPD is a heterogeneous nuclear ribonucleoprotein family member with both cytoplasmic and nuclear roles, and whether HNRNPD regulates the biogenesis of circRNAs remains unknown. In this study, we examine the role of HNRNPD in the biogenesis of ecircRNAs. The levels of ecircRNAs are primarily increased upon depletion of HNRNPD. HNRNPD preferentially binds to motifs enriched with A and U nucleotides, and the flanking introns of ecircRNAs tend to have more numbers and higher intensity of HNRNPD binding sites. The levels of mRNAs are generally not significantly altered in HNRNPD knockout cells. For a small set of genes, the circRNA:mRNA ratio is substantially affected, and the mRNA levels of some of these genes demonstrate a significant decrease in HNRNPD knockout cells. CDK1 is identified as a key gene modulated by HNRNPD in the context of circRNA biogenesis. HNRNPD suppresses the biogenesis of circCDK1 and favours the generation of CDK1 mRNA, and the CDK1 protein is a critical regulator of the cell cycle and apoptosis. HNRNPD can participate in cellular physiology, including the cell cycle and apoptosis, and plays roles in clear cell renal cell carcinoma (ccRCC) by modulating circRNA biogenesis and the mRNA levels of key genes, such as CDK1.
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http://dx.doi.org/10.1080/15476286.2024.2386500 | DOI Listing |
Genes (Basel)
August 2025
Department of Geriatrics, Donald W. Reynolds Institute on Aging, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Alternative splicing is an important mechanism of transcriptomic and proteomic diversity and is progressively involved in cardiovascular disease (CVD) pathogenesis. Serum response factor (SRF), a critical transcription factor in cardiac development and function, may itself undergo splicing regulation, potentially altering its function in disease states. The objective of this study is to identify SRF-associated alternative splicing events in cardiac pathological conditions and examine regulatory interactions with splicing factors using RNA-seq data.
View Article and Find Full Text PDFBiochim Biophys Acta Mol Basis Dis
August 2025
Department of Emergency Medicine, Tri-Service General Hospital, National Defense Medical University, Taipei City 114202, Taiwan, ROC. Electronic address:
Low-density lipoprotein receptors (LDLRs) play a critical role in maintaining cholesterol homeostasis. Dysregulation of lipid metabolism contributes to atherosclerosis and steatohepatitis. This study investigated the effects of nitroxoline on LDLR expression and its protective role in lipid dysregulation, hepatic steatosis, and atherosclerosis.
View Article and Find Full Text PDFPak J Pharm Sci
August 2025
Department of Ophthalmology, The Affiliated People's Hospital of Ningbo University, Ningbo 315040, School of Basic Medical Science, School of Medicine, Ningbo University, Ningbo, Zhejiang, China.
The objective of this study is to investigate the shared genes that are differentially expressed (DEGs) between CES and T2DM, as well as uncover the hidden molecular mechanisms involved. We retrieved the gene expression profiles for CES (GSE58294) and T2DM (GSE25724) from Gene Expression Omnibus (GEO) database. We then per formed 5 analyses: Identify the overlapping DEGs between CES and T2DM, correlation analysis of hub genes; transcriptional regulation analysis of hub genes; single-cell sequencing analysis and potential therapeutic drug prediction.
View Article and Find Full Text PDFJ Med Virol
August 2025
Department of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, China.
Elucidating the molecular mechanisms underlying hepatitis B virus (HBV)-host interactions will hold promise for identifying novel therapeutic targets for HBV. This study aims to investigate the functional interplay and regulatory mechanisms between HBV and the AU-rich element RNA-binding protein 1 (AUF1). We demonstrate that AUF1 inhibits HBV replication and expression in HBV-infected HepG2-NTCP cells, HepG2 cells cotransfected with prcccDNA and pCMV-Cre plasmids, and HepAD38 cells.
View Article and Find Full Text PDFInt Heart J
July 2025
Department of Cardiology, The Second Hospital of Hebei Medical University.
The aim of this study was to investigate the mechanism of m6A methylation in pathological myocardial hypertrophy (PMH), focusing on whether the methyltransferase METTL3 regulates the expression and nuclear translocation of the transcription factor EB (TFEB), thereby affecting autophagic activity and exacerbating the development of myocardial hypertrophy.An in vivo PMH model was established in mice via transverse aortic constriction (TAC), and an in vitro hypertrophy model was established using H9C2 cells stimulated with angiotensin II (AngII). HE staining, Western blotting, qRT-PCR, immunofluorescence, and dual-color autophagy flux analyses were employed to detect the expression of autophagy-related proteins (LC3, Beclin-1, P62, ATG5) and apoptosis levels.
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