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RNA-binding proteins (RBPs) are key regulators of gene expression. Here, we introduce EuPRI (Eukaryotic Protein-RNA Interactions) - a freely available resource of RNA motifs for 34,736 RBPs from 690 eukaryotes. EuPRI includes binding data for 504 RBPs, including newly collected RNAcompete data for 174 RBPs, along with thousands of reconstructed motifs. We reconstruct these motifs with a new computational platform - Joint Protein-Ligand Embedding (JPLE) - which can detect distant homology relationships and map specificity-determining peptides. EuPRI quadruples the number of known RBP motifs, expanding the motif repertoire across all major eukaryotic clades, and assigning motifs to the majority of human RBPs. EuPRI drastically improves knowledge of RBP motifs in flowering plants. For example, it increases the number of RBP motifs 7-fold, from 14 to 105. EuPRI also has broad utility for inferring post-transcriptional function and evolutionary relationships. We demonstrate this by predicting a role for 12 Arabidopsis thaliana RBPs in RNA stability and identifying rapid and recent evolution of post-transcriptional regulatory networks in worms and plants. In contrast, the vertebrate RNA motif set has remained relatively stable after its drastic expansion between the metazoan and vertebrate ancestors. EuPRI represents a powerful resource for the study of gene regulation across eukaryotes.
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http://dx.doi.org/10.1101/2024.10.15.618476 | DOI Listing |
Nat Cell Biol
September 2025
Dioscuri Centre for Chromatin Biology and Epigenomics, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Topologically associating domains (TADs) and chromatin architectural loops impact promoter-enhancer interactions, with CCCTC-binding factor (CTCF) defining TAD borders and loop anchors. TAD boundaries and loops progressively strengthen upon embryonic stem (ES) cell differentiation, underscoring the importance of chromatin topology in ontogeny. However, the mechanisms driving this process remain unclear.
View Article and Find Full Text PDFNature
August 2025
Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Small-cell lung cancers (SCLCs) contain near-universal loss-of-function mutations in RB1 and TP53, compromising the G1-S checkpoint and leading to dysregulated E2F activity. Other cancers similarly disrupt the G1-S checkpoint through loss of CDKN2A or amplification of cyclin D or cyclin E, also resulting in excessive E2F activity. Although E2F activation is essential for cell cycle progression, hyperactivation promotes apoptosis, presenting a therapeutic vulnerability.
View Article and Find Full Text PDFExp Neurol
August 2025
The Third Central Clinical College of Tianjin Medical University, Tianjin 300170, China; Nankai University, Tianjin 300071, China; Department of Anesthesiology, Tianjin University Central Hospital, Tianjin 300170, China; Nankai University Affinity the Third Central Hospital, Tianjin 300170, China; T
Background: Patients with mild cognitive impairment (MCI) before surgery have a higher incidence of perioperative neurocognitive disorders (PND) and a higher rate of progression to dementia than those without MCI; however, the underlying mechanisms are unclear. Heterogeneous nuclear ribonucleoprotein A2/B1 (hnRNPA2/B1) is an RNA-binding protein (RBP) that forms fibrillary tangles via a steric zipper motif. Abnormal accumulation of HnRNPA2/B1 is strongly correlated with local neurodegeneration and cognitive impairment.
View Article and Find Full Text PDFACS Omega
August 2025
School of Computer Science and Technology, Harbin University of Science and Technology, Harbin 150080, China.
The interaction between circular RNAs (circRNAs) and RNA-binding proteins (RBPs) plays a crucial role in gene regulation; however, experimental identification is costly and inefficient. Current computational methods often overlook the structural features of circRNAs, thereby limiting prediction accuracy. To address these challenges, we propose GGCRB, a deep learning framework that integrates both sequence and structural features for predicting circRNA-RBP binding sites.
View Article and Find Full Text PDFPUF proteins (named for Pumilio and mRNA binding factor or FBF) are a family of RNA-binding proteins. FBF is a collective term for two PUF proteins, FBF-1 and FBF-2, that maintain germline stem cells. FBF binds the 3'UTR of target RNAs and together with partner proteins represses translation of mRNAs that promote differentiation.
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