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Apolipoprotein B-editing enzyme, catalytic polypeptide-1 (APOBEC1) is a cytidine deaminase initially identified by its activity in converting a specific cytidine (C) to uridine (U) in apolipoprotein B (apoB) mRNA transcripts in the small intestine. Editing results in the translation of a truncated apoB isoform with distinct functions in lipid transport. To address the possibility that APOBEC1 edits additional mRNAs, we developed a transcriptome-wide comparative RNA sequencing (RNA-Seq) screen. We identified and validated 32 previously undescribed mRNA targets of APOBEC1 editing, all of which are located in AU-rich segments of transcript 3' untranslated regions (3' UTRs). Further analysis established several characteristic sequence features of editing targets, which were predictive for the identification of additional APOBEC1 substrates. The transcriptomics approach to RNA editing presented here dramatically expands the list of APOBEC1 mRNA editing targets and reveals a novel cellular mechanism for the modification of transcript 3' UTRs.
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http://dx.doi.org/10.1038/nsmb.1975 | DOI Listing |
Mol Plant
September 2025
College of Life Sciences, Capital Normal University, Beijing, 100048, China; Beijing Key Laboratory of Plant Gene Resources and Biotechnology for Carbon Reduction and Environmental Improvement, Beijing, 100048, China. Electronic address:
In the intricate molecular warfare between plants and pathogens, bacteria deploy sophisticated strategies to subvert host defenses. Xanthomonas oryzae pathogens, which cause devastating bacterial blight (BB) and bacterial leaf streak (BLS) in rice, utilize transcription activator-like effectors (TALEs) to manipulate host gene expression. Secreted by the type III secretion system and translocated by the type III translocon into host cells, TALEs directly bind specific DNA sequences (effector-binding elements, EBEs) in the 5'-terminal untranslated regions (UTRs) or within the promoter regions of host genes to activate transcription of these genes, including SWEETs sugar transporters and negative regulators of plant immunity (Xue et al.
View Article and Find Full Text PDFFront Immunol
September 2025
Department of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, CT, United States.
Introduction: CCR2, a chemokine receptor critical for immune cell migration, inflammation, and HIV infection, is regulated by poorly understood mechanisms.
Methods: This study investigated the unusually long CCR2 3'-UTR's role in post-transcriptional regulation.
Results: The full-length 3'-UTR significantly inhibited reporter gene expression in primary CD4+ T cells and macrophages, likely mediated by RNA binding proteins (RBPs).
Nucleic Acids Res
August 2025
Department of Chemistry and State Key Laboratory of Marine Environmental Health, City University of Hong Kong, Hong Kong SAR, 000000, China.
TDP-43 is a hallmark protein associated with neurodegenerative diseases. Recent studies revealed TDP-43 as an RNA G-quadruplex (rG4)-binding protein, impacting mRNA transport and function. However, our knowledge of the TDP-43-RNA secondary structure interaction and information on its specific rG4 targets are limited.
View Article and Find Full Text PDFMob DNA
September 2025
Laboratory of Cancer Epigenetics and Plasticity, Brown University, Providence, RI, USA.
Background: Glioblastoma, the most common primary malignant brain tumor, has a median survival of less than two years. This is due in part to a subpopulation of cells called glioblastoma stem cells (GSCs), which drive tumor recurrence. Transposable elements (TEs) are expressed at higher levels in cancer stem cells, enhancing the oncogenic potential and plasticity of cells through changes in gene expression, fusion transcript generation, and genomic rearrangement.
View Article and Find Full Text PDFFront Cell Infect Microbiol
September 2025
Department of Pathogen Biology, School of Medicine, Nantong University, Nantong, Jiangsu, China.
Introduction: , a zoonotic parasitic disease, induces complex immune regulation during infection. The inflammatory responses and immunosuppressive mechanisms co-exist to maintain immune homeostasis in schistosomiasis. B7-H4 is a critical immune checkpoint molecule that modulates T cell activation and exerts immunosuppressive effects.
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