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206 results for “protein”

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  1. Inhibition of YTHDF2 triggers proteotoxic cell death in MYC-driven breast cancer.

    Molecular cell · 2021 · 81(15): 3048-3064.e9

    RNA-binding proteins (RBPs) are critical regulators of post-transcriptional gene expression, and aberrant RBP-RNA interactions can promote cancer progression. Here, we interrogate the function of RBPs in cancer using pooled CRISPR-Cas9 screening and identify 57 RBP candidates with distinct roles in …

    PMID 34216543 DOI ↗

  2. Huntington's disease mice and human brain tissue exhibit increased G3BP1 granules and TDP43 mislocalization.

    The Journal of clinical investigation · 2021 · 131(12)

    Chronic cellular stress associated with neurodegenerative disease can result in the persistence of stress granule (SG) structures, membraneless organelles that form in response to cellular stress. In Huntington's disease (HD), chronic expression of mutant huntingtin generates various forms of cellular …

    PMID 33945510 DOI ↗

  3. Robust single-cell discovery of RNA targets of RNA-binding proteins and ribosomes.

    Nature methods · 2021 · 18(5): 507-519

    RNA-binding proteins (RBPs) are critical regulators of gene expression and RNA processing that are required for gene function. Yet the dynamics of RBP regulation in single cells is unknown. To address this gap in understanding, we developed STAMP (Surveying Targets …

    PMID 33963355 DOI ↗

  4. S-nitrosylated TDP-43 triggers aggregation, cell-to-cell spread, and neurotoxicity in hiPSCs and in vivo models of ALS/FTD.

    Proceedings of the National Academy of Sciences of the United States of America · 2021 · 118(11)

    Rare genetic mutations result in aggregation and spreading of cognate proteins in neurodegenerative disorders; however, in the absence of mutation (i.e., in the vast majority of "sporadic" cases), mechanisms for protein misfolding/aggregation remain largely unknown. Here, we show environmentally induced …

    PMID 33692125 DOI ↗

  5. A CRISPR RNA-binding protein screen reveals regulators of RUNX1 isoform generation.

    Blood advances · 2021 · 5(5): 1310-1323

    The proper balance of hematopoietic stem cell (HSC) self-renewal and differentiation is critical for normal hematopoiesis and is disrupted in hematologic malignancy. Among regulators of HSC fate, transcription factors have a well-defined central role, and mutations promote malignant transformation. More …

    PMID 33656539 DOI ↗

  6. The sustained expression of Cas9 targeting toxic RNAs reverses disease phenotypes in mouse models of myotonic dystrophy type 1.

    Nature biomedical engineering · 2021 · 5(2): 157-168

    Myotonic dystrophy type I (DM1) is a multisystemic autosomal-dominant inherited human disorder that is caused by CTG microsatellite repeat expansions (MREs) in the 3' untranslated region of DMPK. Toxic RNAs expressed from such repetitive sequences can be eliminated using CRISPR-mediated …

    PMID 32929188 DOI ↗

  7. Reintroduction of the archaic variant of <i>NOVA1</i> in cortical organoids alters neurodevelopment.

    Science (New York, N.Y.) · 2021 · 371(6530)

    The evolutionarily conserved splicing regulator neuro-oncological ventral antigen 1 (<i>NOVA1</i>) plays a key role in neural development and function. <i>NOVA1</i> also includes a protein-coding difference between the modern human genome and Neanderthal and Denisovan genomes. To investigate the functional importance …

    PMID 33574182 DOI ↗

  8. Author Correction: A large-scale binding and functional map of human RNA-binding proteins.

    Nature · 2021 · 589(7842): E5

    PMID 33402748 DOI ↗

  9. Transcriptome-wide profiles of circular RNA and RNA-binding protein interactions reveal effects on circular RNA biogenesis and cancer pathway expression.

    Genome medicine · 2020 · 12(1): 112

    Circular RNAs (circRNAs) are stable, often highly expressed RNA transcripts with potential to modulate other regulatory RNAs. A few circRNAs have been shown to bind RNA-binding proteins (RBPs); however, little is known about the prevalence and distribution of these interactions …

    PMID 33287884 DOI ↗

  10. Footprinting SHAPE-eCLIP Reveals Transcriptome-wide Hydrogen Bonds at RNA-Protein Interfaces.

    Molecular cell · 2020 · 80(5): 903-914.e8

    Discovering the interaction mechanism and location of RNA-binding proteins (RBPs) on RNA is critical for understanding gene expression regulation. Here, we apply selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) on in vivo transcripts compared to protein-absent transcripts in four …

    PMID 33242392 DOI ↗

  11. The <i>Thermus thermophilus</i> DEAD-box protein Hera is a general RNA binding protein and plays a key role in tRNA metabolism.

    RNA (New York, N.Y.) · 2020 · 26(11): 1557-1574

    RNA helicases catalyze the ATP-dependent destabilization of RNA duplexes. DEAD-box helicases share a helicase core that mediates ATP binding and hydrolysis, RNA binding and unwinding. Most members of this family contain domains flanking the core that can confer RNA substrate …

    PMID 32669294 DOI ↗

  12. Zmat3 Is a Key Splicing Regulator in the p53 Tumor Suppression Program.

    Molecular cell · 2020 · 80(3): 452-469.e9

    Although TP53 is the most commonly mutated gene in human cancers, the p53-dependent transcriptional programs mediating tumor suppression remain incompletely understood. Here, to uncover critical components downstream of p53 in tumor suppression, we perform unbiased RNAi and CRISPR-Cas9-based genetic screens …

    PMID 33157015 DOI ↗

  13. Evaluation of Engineered CRISPR-Cas-Mediated Systems for Site-Specific RNA Editing.

    Cell reports · 2020 · 33(5): 108350

    Site-directed RNA editing approaches offer great potential to correct genetic mutations in somatic cells while avoiding permanent off-target genomic edits. Nuclease-dead RNA-targeting CRISPR-Cas systems recruit functional effectors to RNA molecules in a programmable fashion. Here, we demonstrate a Streptococcus pyogenes …

    PMID 33147453 DOI ↗

  14. Large-scale tethered function assays identify factors that regulate mRNA stability and translation.

    Nature structural & molecular biology · 2020 · 27(10): 989-1000

    The molecular functions of the majority of RNA-binding proteins (RBPs) remain unclear, highlighting a major bottleneck to a full understanding of gene expression regulation. Here, we develop a plasmid resource of 690 human RBPs that we subject to luciferase-based 3'-untranslated-region …

    PMID 32807991 DOI ↗

  15. DDX5 promotes oncogene C3 and FABP1 expressions and drives intestinal inflammation and tumorigenesis.

    Life science alliance · 2020 · 3(10)

    Tumorigenesis in different segments of the intestinal tract involves tissue-specific oncogenic drivers. In the colon, complement component 3 (C3) activation is a major contributor to inflammation and malignancies. By contrast, tumorigenesis in the small intestine involves fatty acid-binding protein 1 …

    PMID 32817263 DOI ↗

  16. Context-dependent functional compensation between Ythdf m<sup>6</sup>A reader proteins.

    Genes & development · 2020 · 34(19-20): 1373-1391

    The N6-methyladenosine (m<sup>6</sup>A) modification is the most prevalent post-transcriptional mRNA modification, regulating mRNA decay and splicing. It plays a major role during normal development, differentiation, and disease progression. The modification is regulated by a set of writer, eraser, and reader …

    PMID 32943573 DOI ↗

  17. G<sub>4</sub>C<sub>2</sub> Repeat RNA Initiates a POM121-Mediated Reduction in Specific Nucleoporins in C9orf72 ALS/FTD.

    Neuron · 2020 · 107(6): 1124-1140.e11

    Through mechanisms that remain poorly defined, defects in nucleocytoplasmic transport and accumulations of specific nuclear-pore-complex-associated proteins have been reported in multiple neurodegenerative diseases, including C9orf72 Amyotrophic Lateral Sclerosis and Frontotemporal Dementia (ALS/FTD). Using super-resolution structured illumination microscopy, we have explored …

    PMID 32673563 DOI ↗

  18. Transcriptome-wide analysis of PGC-1α-binding RNAs identifies genes linked to glucagon metabolic action.

    Proceedings of the National Academy of Sciences of the United States of America · 2020 · 117(36): 22204-22213

    The peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) is a transcriptional coactivator that controls expression of metabolic/energetic genes, programming cellular responses to nutrient and environmental adaptations such as fasting, cold, or exercise. Unlike other coactivators, PGC-1α contains protein domains involved …

    PMID 32848060 DOI ↗

  19. Motoneuron expression profiling identifies an association between an axonal splice variant of HDGF-related protein 3 and peripheral myelination.

    The Journal of biological chemistry · 2020 · 295(34): 12233-12246

    Disorders that disrupt myelin formation during development or in adulthood, such as multiple sclerosis and peripheral neuropathies, lead to severe pathologies, illustrating myelin's crucial role in normal neural functioning. However, although our understanding of glial biology is increasing, the signals …

    PMID 32647008 DOI ↗

  20. A role for alternative splicing in circadian control of exocytosis and glucose homeostasis.

    Genes & development · 2020 · 34(15-16): 1089-1105

    The circadian clock is encoded by a negative transcriptional feedback loop that coordinates physiology and behavior through molecular programs that remain incompletely understood. Here, we reveal rhythmic genome-wide alternative splicing (AS) of pre-mRNAs encoding regulators of peptidergic secretion within pancreatic …

    PMID 32616519 DOI ↗

  21. A large-scale binding and functional map of human RNA-binding proteins.

    Nature · 2020 · 583(7818): 711-719

    Many proteins regulate the expression of genes by binding to specific regions encoded in the genome<sup>1</sup>. Here we introduce a new data set of RNA elements in the human genome that are recognized by RNA-binding proteins (RBPs), generated as part …

    PMID 32728246 DOI ↗

  22. Expanded encyclopaedias of DNA elements in the human and mouse genomes.

    Nature · 2020 · 583(7818): 699-710

    The human and mouse genomes contain instructions that specify RNAs and proteins and govern the timing, magnitude, and cellular context of their production. To better delineate these elements, phase III of the Encyclopedia of DNA Elements (ENCODE) Project has expanded …

    PMID 32728249 DOI ↗

  23. Pooled CRISPR screens with imaging on microraft arrays reveals stress granule-regulatory factors.

    Nature methods · 2020 · 17(6): 636-642

    Genetic screens using pooled CRISPR-based approaches are scalable and inexpensive, but restricted to standard readouts, including survival, proliferation and sortable markers. However, many biologically relevant cell states involve cellular and subcellular changes that are only accessible by microscopic visualization, and …

    PMID 32393832 DOI ↗

  24. An in vivo genome-wide CRISPR screen identifies the RNA-binding protein Staufen2 as a key regulator of myeloid leukemia.

    Nature cancer · 2020 · 1(4): 410-422

    Aggressive myeloid leukemias such as blast crisis chronic myeloid leukemia and acute myeloid leukemia remain highly lethal. Here we report a genome-wide in vivo CRISPR screen to identify new dependencies in this disease. Among these, RNA-binding proteins (RBPs) in general, …

    PMID 34109316 DOI ↗

  25. Principles of RNA processing from analysis of enhanced CLIP maps for 150 RNA binding proteins.

    Genome biology · 2020 · 21(1): 90

    A critical step in uncovering rules of RNA processing is to study the in vivo regulatory networks of RNA binding proteins (RBPs). Crosslinking and immunoprecipitation (CLIP) methods enable mapping RBP targets transcriptome-wide, but methodological differences present challenges to large-scale analysis …

    PMID 32252787 DOI ↗

Datasets 25+

GSE302600 GSE · GEO

Zfp697/ZNF697 is an RNA-binding protein that modulates TGF-β1 2 signaling and hepatic inflammation in liver disease

Mus musculus · GPL30172

GSE254209 GSE · GEO

Inhibition of RNA splicing triggers CHMP7 nuclear entry impacting TDP-43 function and leading to onset of ALS (eCLIP).

Homo sapiens · GPL24676

GSE254208 GSE · GEO

Inhibition of RNA splicing triggers CHMP7 nuclear entry impacting TDP-43 function and leading to onset of ALS (RNA-Seq).

Homo sapiens · Illumina

GSE328331 GSE · GEO

Modulation of the DNA/RNA Binding Protein ARID5A Regulates Microglial Activation and Response [RIP-Seq]

Homo sapiens · Illumina

GSE290625 GSE · GEO

Modulation of the DNA/RNA Binding Protein ARID5A Regulates Microglial Activation and Response [eclip]

Homo sapiens · Illumina

GSE290765 GSE · GEO

Modulation of the DNA/RNA Binding Protein ARID5A Regulates Microglial Activation and Response [cutnrun]

Homo sapiens · Illumina

GSE290755 GSE · GEO

Modulation of the DNA/RNA Binding Protein ARID5A Regulates Microglial Activation and Response [rna-seq]

Homo sapiens · Illumina

GSE227455 GSE · GEO

RBP Footprint Grand Challenge: An evaluation of novel computational approaches to RNA-binding protein target prediction from structural data

Homo sapiens · GPL20301

GSE145805 GSE · GEO

RNA secondary structome of different cell lines

Homo sapiens, Mus musculus · GPL20795, GPL21273

GSE302649 GSE · GEO

Mapping CCR4-NOT recruitment elements at high resolution reveals transcriptome-wide determinants of mRNA decay [miRNA-Seq]

GPL18573

GSE302648 GSE · GEO

Mapping CCR4-NOT recruitment elements at high resolution reveals transcriptome-wide determinants of mRNA decay [RIP-Seq]

GPL18573

GSE290248 GSE · GEO

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection [PAS-seq]

Homo sapiens · Illumina

GSE290282 GSE · GEO

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection [RNA-Seq]

Homo sapiens · Illumina

GSE290281 GSE · GEO

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection [eCLIP]

Homo sapiens · Illumina

GSE244832 GSE · GEO

Multi-Modal Comparison of human Hepatic Stellate Cells identifies novel therapeutic targets for Metabolic Dysfunction-Associated Steatotic Liver Disease

Homo sapiens · GPL24676, GPL37309

GSE151788 GSE · GEO

Ythdf m6A readers compensate each other in a context dependent manner [eCLIP]

GPL17021

GSE148536 GSE · GEO

Ythdf m6A readers compensate each other in a context dependent manner [Ribo-seq]

GPL21626

GSE148038 GSE · GEO

Ythdf m6A readers compensate each other in a context dependent manner [3'UTR RNA-seq]

GPL13112

GSE147849 GSE · GEO

Ythdf m6A readers compensate each other in a context dependent manner [RNA-seq]

GPL21626

GSE315443 GSE · GEO

MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy [scRNA-Seq]

GPL24676

GSE315407 GSE · GEO

Comprehensive RNA-binding protein analyses using enhanced CLIP (ENCORE)

GPL20301, GPL24676, GPL34284

GSE315406 GSE · GEO

Comprehensive RNA-binding protein analyses using enhanced CLIP (ENCORE) [dataset2]

GPL20301, GPL24676, GPL34284

GSE315347 GSE · GEO

Comprehensive RNA-binding protein analyses using enhanced CLIP (ENCORE) [dataset1]

GPL20301, GPL24676

GSE315026 GSE · GEO

MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy [eCLIP]

GPL24676

GSE314059 GSE · GEO

Single-cell and isoform-specific translational profiling of the mouse brain with long-read sequencing [scRNA-Seq, longread]

GPL34585

Showing first 25 dataset results.

Analyses 25+

GSE244832 scRNA-seq Data Processing

GSE244832 · 9 steps · scRNA-seq · geo_data_processing

RNA-binding protein LARP6 coordinates hepatic stellate cell activation and liver fibrosis. (2026)

GSE290248 Data Processing

GSE290248 · 1 step · geo_data_processing

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection. (2026)

GSE290281 eCLIP Data Processing

GSE290281 · 1 step · eCLIP · geo_data_processing

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection. (2026)

GSE290282 RNA-seq Data Processing

GSE290282 · 3 steps · RNA-seq · geo_data_processing

Large-scale tethered screen of RNA-binding proteins reveals novel regulators of poly(A) site selection. (2026)

GSE299099 Processing Pipeline

GSE299099 · 3 steps · RNA-Seq · code_examples

Structural and mechanistic analysis of covalent ligands targeting the RNA-binding protein NONO. (2026)

GSE315347 eCLIP Data Processing

GSE315347 · 4 steps · eCLIP · geo_data_processing

Comprehensive RNA-binding protein analyses and deep learning uncover genetic constraints and disease associations in protein-RNA interfaces. (2026)

GSE315406 eCLIP Data Processing

GSE315406 · 4 steps · eCLIP · geo_data_processing

Comprehensive RNA-binding protein analyses and deep learning uncover genetic constraints and disease associations in protein-RNA interfaces. (2026)

GSE315407 eCLIP Data Processing

GSE315407 · 4 steps · eCLIP · geo_data_processing

Comprehensive RNA-binding protein analyses and deep learning uncover genetic constraints and disease associations in protein-RNA interfaces. (2026)

GSE145805 SHAPE-seq Data Processing

GSE145805 · 7 steps · SHAPE-seq · geo_data_processing

Evaluation of novel computational methods to identify RNA-binding protein footprints from structural data. (2025)

GSE227455 eCLIP Data Processing

GSE227455 · 7 steps · eCLIP · geo_data_processing

Evaluation of novel computational methods to identify RNA-binding protein footprints from structural data. (2025)

GSE262542 Processing Pipeline

GSE262542 · 4 steps · RNA-Seq · code_examples

Evaluation of novel computational methods to identify RNA-binding protein footprints from structural data. (2025)

GSE276985 Processing Pipeline

GSE276985 · 2 steps · RIP-Seq · code_examples

Neuronal aging causes mislocalization of splicing proteins and unchecked cellular stress. (2025)

GSE276986 Processing Pipeline

GSE276986 · 1 step · RNA-Seq · code_examples

Neuronal aging causes mislocalization of splicing proteins and unchecked cellular stress. (2025)

GSE277082 Processing Pipeline

GSE277082 · 2 steps · RNA-Seq · code_examples

Neuronal aging causes mislocalization of splicing proteins and unchecked cellular stress. (2025)

GSE106493 Processing Pipeline

GSE106493 · 4 steps · RIP-Seq · code_examples

Transcriptome regulation by PARP13 in basal and antiviral states in human cells. (2024)

GSE114820 Processing Pipeline

GSE114820 · 4 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE143437 Processing Pipeline

GSE143437 · 7 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE145480 Processing Pipeline

GSE145480 · 11 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE147127 Processing Pipeline

GSE147127 · 5 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE193134 Processing Pipeline

GSE193134 · 18 steps · RIP-Seq · code_examples

LARP4 is an RNA-binding protein that binds nuclear-encoded mitochondrial mRNAs to promote mitochondrial function. (2024)

GSE210263 Processing Pipeline

GSE210263 · 10 steps · RNA-Seq · code_examples

Zfp697 is an RNA-binding protein that regulates skeletal muscle inflammation and remodeling. (2024)

GSE230097 Processing Pipeline

GSE230097 · 6 steps · RNA-Seq · code_examples

ePRINT: exonuclease assisted mapping of protein-RNA interactions. (2024)

GSE230717 Processing Pipeline

GSE230717 · 9 steps · RIP-Seq · code_examples

Large-scale map of RNA-binding protein interactomes across the mRNA life cycle. (2024)

GSE232513 Processing Pipeline

GSE232513 · 3 steps · RNA-Seq · code_examples

High-sensitivity in situ capture of endogenous RNA-protein interactions in fixed cells and primary tissues. (2024)

GSE232514 Processing Pipeline

GSE232514 · 5 steps · RNA-Seq · code_examples

High-sensitivity in situ capture of endogenous RNA-protein interactions in fixed cells and primary tissues. (2024)

Showing first 25 analysis results.