Transcription factors (TFs) are key regulators of gene expression, yet many of their targets and modes of action remain unknown. In Schizosaccharomyces pombe, one-third of TFs are solely homology predicted, with few experimentally validated. We created a comprehensive library of 89 endogenously tagged S. pombe TFs, mapping their protein and chromatin interactions using immunoprecipitation-mass spectrometry and chromatin immunoprecipitation sequencing. Our study identified protein interactors for half the TFs, with over a quarter potentially forming stable complexes. We discovered DNA-binding sites for most TFs across 2,027 unique genomic regions, revealing motifs for 38 TFs and uncovering a complex network of extensive TF cross- and autoregulation. Characterization of the largest TF family revealed conserved DNA sequence preferences but diverse binding patterns and identified a repressive heterodimer, Ntu1/Ntu2, linked to perinuclear gene localization. Our TFexplorer webtool makes all data interactively accessible, offering insights into TF interactions and regulatory mechanisms with broad biological relevance.
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http://dx.doi.org/10.1016/j.molcel.2025.01.032 | DOI Listing |
Commun Biol
March 2025
Institute of Molecular Biology, Biocenter, Medical University Innsbruck, Innsbruck, Austria.
Iron homeostasis is key to both the survival of virtually all organisms and the virulence of fungi including Aspergillus fumigatus, a human fungal pathogen causing life-threatening invasive infections. Unlike the extensively studied fungal species Saccharomyces cerevisiae and Schizosaccharomyces pombe, A. fumigatus encodes an uncharacterized homolog of vertebrate ferroportin (Fpn1), termed FpnA.
View Article and Find Full Text PDFJ Mol Biol
March 2025
School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore 637551 Singapore; Mechanobiology Institute, National University of Singapore, Singapore 117411 Singapore.
Biomedical literature contains an extensive wealth of information on gene and protein function across various biological processes and diseases. However, navigating this vast and often restricted-access data can be challenging, making it difficult to extract specific insights efficiently. In this study, we introduce a high-throughput pipeline that leverages OpenAI's Generative Pre-Trained Transformer Model (GPT) to automate the extraction and analysis of gene function information.
View Article and Find Full Text PDFNucleic Acids Res
February 2025
Institute of Biochemical Sciences, National Taiwan University, Taipei 10617, Taiwan.
During meiosis, programmed DNA double-strand breaks (DSBs) are formed at hotspots to initiate homologous recombination, which is vital for reassorting genetic material. In fission yeast, the linear element (LinE) proteins Mug20, Rec25, and Rec27 interdependently bind chromosomal hotspots with high specificity and are necessary for high-level DSB formation. However, their mechanistic role in regulating the meiotic DSB machinery remains unknown.
View Article and Find Full Text PDFbioRxiv
February 2025
Department of Biological Sciences, Lehigh University, Bethlehem, Pennsylvania, USA.
The telomerase RNA-protein enzyme is critical for most eukaryotes to complete genome copying by extending chromosome ends, thus solving the end-replication problem and postponing senescence. Despite the importance of the fission yeast to biomedical research, very little is known about the structure of its 1212 nt telomerase RNA. We have determined the secondary structure of this large RNA, TER1, based on phylogenetics and bioinformatic modeling, as well as genetic and biochemical analyses.
View Article and Find Full Text PDFMicroPubl Biol
February 2025
Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN, US.
The septation initiation network (SIN) is required for cytokinesis and septation. The SIN includes a protein kinase cascade that is assembled at spindle pole bodies (SPBs) in a cell cycle specific manner on a scaffold consisting of Cdc11 , related to human centriolin, and the a-helical protein Sid4 . Here, we characterized temperature-sensitive and mutants isolated in the 1990s.
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