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Synaptic accumulation of FUS triggers age-dependent misregulation of inhibitory synapses in ALS-FUS mice

https://doi.org/10.1101/2020.06.10.136010

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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GABA A ‐receptor heterogeneity in the adult rat brain: Differential regional and cellular distribution of seven major subunits

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FUS/TLS assembles into stress granules and is a prosurvival factor during hyperosmolar stress

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The function of RNA-binding proteins at the synapse: implications for neurodegeneration

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Contribution of GABAA receptors containing α3 subunits to the therapeutic-related and side effects of benzodiazepine-type drugs in monkeys

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Localization of fused in sarcoma (FUS) protein to the post-synaptic density in the brain

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Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosis

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Synaptic dysfunction and altered excitability in C9ORF72 ALS/FTD

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Driven to decay: Excitability and synaptic abnormalities in amyotrophic lateral sclerosis

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Rules for Nuclear Localization Sequence Recognition by Karyopherinβ2

inferredcites →https://doi.org/10.1016/j.cell.2015.07.047openalex-snapshot

A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation

inferredcites →https://doi.org/10.1016/j.cell.2018.03.002openalex-snapshot

Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains

inferredcites →https://doi.org/10.1016/j.cell.2018.03.003openalex-snapshot

Nuclear Import Receptor Inhibits Phase Separation of FUS through Binding to Multiple Sites

inferredcites →https://doi.org/10.1016/j.cell.2018.03.004openalex-snapshot

Phase Separation of FUS Is Suppressed by Its Nuclear Import Receptor and Arginine Methylation

inferredcites →https://doi.org/10.1016/j.cell.2018.03.056openalex-snapshot

FUS Phase Separation Is Modulated by a Molecular Chaperone and Methylation of Arginine Cation-π Interactions

inferredcites →https://doi.org/10.1016/j.celrep.2017.08.100openalex-snapshot

3′UTR Length-Dependent Control of SynGAP Isoform α2 mRNA by FUS and ELAV-like Proteins Promotes Dendritic Spine Maturation and Cognitive Function

inferredcites →https://doi.org/10.1016/j.celrep.2018.06.094openalex-snapshot

Hypertonic Stress Causes Cytoplasmic Translocation of Neuronal, but Not Astrocytic, FUS due to Impaired Transportin Function

inferredcites →https://doi.org/10.1016/j.celrep.2020.02.026openalex-snapshot

Neuronal BIN1 Regulates Presynaptic Neurotransmitter Release and Memory Consolidation

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Local translation in neuronal processes

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The RNA Binding Protein TLS Is Translocated to Dendritic Spines by mGluR5 Activation and Regulates Spine Morphology

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Interplay of Hippocampus and Prefrontal Cortex in Memory

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Simple Combinations of Lineage-Determining Transcription Factors Prime cis-Regulatory Elements Required for Macrophage and B Cell Identities

inferredcites →https://doi.org/10.1016/j.molcel.2018.11.012openalex-snapshot

The Solution Structure of FUS Bound to RNA Reveals a Bipartite Mode of RNA Recognition with Both Sequence and Shape Specificity

inferredcites →https://doi.org/10.1016/j.neuron.2006.04.016openalex-snapshot

A Shared Vesicular Carrier Allows Synaptic Corelease of GABA and Glycine

inferredcites →https://doi.org/10.1016/j.neuron.2012.02.036openalex-snapshot

The Local Transcriptome in the Synaptic Neuropil Revealed by Deep Sequencing and High-Resolution Imaging

inferredcites →https://doi.org/10.1016/j.neuron.2013.03.009openalex-snapshot

Nanoscale Scaffolding Domains within the Postsynaptic Density Concentrate Synaptic AMPA Receptors

inferredcites →https://doi.org/10.1016/j.neuron.2013.05.013openalex-snapshot

Quantitative Nanoscopy of Inhibitory Synapses: Counting Gephyrin Molecules and Receptor Binding Sites

inferredcites →https://doi.org/10.1016/j.neuron.2015.10.030openalex-snapshot

ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function

inferredcites →https://doi.org/10.1016/j.neuron.2016.11.002openalex-snapshot

Life at Low Copy Number: How Dendrites Manage with So Few mRNAs

inferredcites →https://doi.org/10.1016/j.neuron.2018.07.007openalex-snapshot

Architecture of the Mouse Brain Synaptome

inferredcites →https://doi.org/10.1016/j.neuron.2018.09.044openalex-snapshot

ALS/FTD-Linked Mutation in FUS Suppresses Intra-axonal Protein Synthesis and Drives Disease Without Nuclear Loss-of-Function of FUS

inferredcites →https://doi.org/10.1016/j.neuron.2018.10.018openalex-snapshot

The AMPA Receptor Code of Synaptic Plasticity

inferredcites →https://doi.org/10.1016/j.neuropharm.2012.03.001openalex-snapshot

Benzodiazepine-induced anxiolysis and reduction of conditioned fear are mediated by distinct GABAA receptor subtypes in mice

inferredcites →https://doi.org/10.1016/j.tins.2014.05.009openalex-snapshot

The multifunctional Staufen proteins: conserved roles from neurogenesis to synaptic plasticity

inferredcites →https://doi.org/10.1016/s0165-0173(97)00061-1openalex-snapshot

Salient features of synaptic organisation in the cerebral cortex1Published on the World Wide Web on 3 March 1998.1

inferredcites →https://doi.org/10.1016/s1474-4422(10)70195-2openalex-snapshot

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

inferredcites →https://doi.org/10.1038/72842openalex-snapshot

Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death

inferredcites →https://doi.org/10.1038/76615openalex-snapshot

Proteomic analysis of NMDA receptor–adhesion protein signaling complexes

inferredcites →https://doi.org/10.1038/emboj.2010.143openalex-snapshot

ALS‐associated fused in sarcoma (FUS) mutations disrupt Transportin‐mediated nuclear import

inferredcites →https://doi.org/10.1038/emm.2015.5openalex-snapshot

Gephyrin: a central GABAergic synapse organizer

inferredcites →https://doi.org/10.1038/ncomms8098openalex-snapshot

FUS regulates AMPA receptor function and FTLD/ALS-associated behaviour via GluA1 mRNA stabilization

inferredcites →https://doi.org/10.1038/nmeth.4197openalex-snapshot

Salmon provides fast and bias-aware quantification of transcript expression

inferredcites →https://doi.org/10.1038/nn.2779openalex-snapshot

Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43

inferredcites →https://doi.org/10.1038/nn.3230openalex-snapshot

Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs

inferredcites →https://doi.org/10.1038/nn.3514openalex-snapshot

Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons

inferredcites →https://doi.org/10.1038/nsmb.2163openalex-snapshot

RNA targets of wild-type and mutant FET family proteins

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Rbfox proteins regulate alternative mRNA splicing through evolutionarily conserved RNA bridges

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Local translation in neurons: visualization and function

inferredcites →https://doi.org/10.1038/s41598-017-01175-8openalex-snapshot

The tandem Agenet domain of fragile X mental retardation protein interacts with FUS

inferredcites →https://doi.org/10.1038/s41598-018-25007-5openalex-snapshot

Nuclear egress of TDP-43 and FUS occurs independently of Exportin-1/CRM1

inferredcites →https://doi.org/10.1038/s41598-019-42833-3openalex-snapshot

SNAP-25 isoforms differentially regulate synaptic transmission and long-term synaptic plasticity at central synapses

inferredcites →https://doi.org/10.1038/srep00529openalex-snapshot

Position-dependent FUS-RNA interactions regulate alternative splicing events and transcriptions

inferredcites →https://doi.org/10.1038/srep00603openalex-snapshot

Widespread binding of FUS along nascent RNA regulates alternative splicing in the brain

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Lithium storage mechanisms in purpurin based organic lithium ion battery electrodes

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Dual-color STED microscopy reveals a sandwich structure of Bassoon and Piccolo in active zones of adult and aged mice

inferredcites →https://doi.org/10.1042/bst0310865openalex-snapshot

Assembly of N-methyl-d-aspartate (NMDA) receptors

inferredcites →https://doi.org/10.1073/pnas.1715341114openalex-snapshot

Intersectin associates with synapsin and regulates its nanoscale localization and function

inferredcites →https://doi.org/10.1074/jbc.m111.291336openalex-snapshot

Molecular Basis of the γ-Aminobutyric Acid A Receptor α3 Subunit Interaction with the Clustering Protein Gephyrin

inferredcites →https://doi.org/10.1074/jbc.r112.386664openalex-snapshot

Structure, Function, and Modulation of GABAA Receptors

inferredcites →https://doi.org/10.1083/jcb.201302071openalex-snapshot

Local palmitoylation cycles define activity-regulated postsynaptic subdomains

inferredcites →https://doi.org/10.1093/bioinformatics/btq033openalex-snapshot

BEDTools: a flexible suite of utilities for comparing genomic features

inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-snapshot

STAR: ultrafast universal RNA-seq aligner

inferredcites →https://doi.org/10.1093/brain/awp214openalex-snapshot

A new subtype of frontotemporal lobar degeneration with FUS pathology

inferredcites →https://doi.org/10.1093/hmg/ddq137openalex-snapshot

TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration

inferredcites →https://doi.org/10.1093/hmg/ddx415openalex-snapshot

Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice

inferredcites →https://doi.org/10.1093/nar/gks042openalex-snapshot

Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation

inferredcites →https://doi.org/10.1093/nar/gkt835openalex-snapshot

PARP-1 dependent recruitment of the amyotrophic lateral sclerosis-associated protein FUS/TLS to sites of oxidative DNA damage

inferredcites →https://doi.org/10.1101/gad.204602.112openalex-snapshot

FUS binds the CTD of RNA polymerase II and regulates its phosphorylation at Ser2

inferredcites →https://doi.org/10.1101/gad.255737.114openalex-snapshot

Position-specific binding of FUS to nascent RNA regulates mRNA length

inferredcites →https://doi.org/10.1126/science.1074069openalex-snapshot

Alzheimer's Disease Is a Synaptic Failure

inferredcites →https://doi.org/10.1126/science.1165942openalex-snapshot

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

inferredcites →https://doi.org/10.1126/science.1166066openalex-snapshot

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

inferredcites →https://doi.org/10.1126/science.aar7366openalex-snapshot

RNA buffers the phase separation behavior of prion-like RNA binding proteins

inferredcites →https://doi.org/10.1126/science.aar7432openalex-snapshot

mRNA structure determines specificity of a polyQ-driven phase separation

inferredcites →https://doi.org/10.1126/science.aav2642openalex-snapshot

The forebrain synaptic transcriptome is organized by clocks but its proteome is driven by sleep

inferredcites →https://doi.org/10.1126/science.aav3617openalex-snapshot

Sleep-wake cycles drive daily dynamics of synaptic phosphorylation

inferredcites →https://doi.org/10.1128/mcb.00884-09openalex-snapshot

TLS Inhibits RNA Polymerase III Transcription

inferredcites →https://doi.org/10.1186/1471-2121-9-37openalex-snapshot

The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response

inferredcites →https://doi.org/10.1186/gb-2010-11-2-r14openalex-snapshot

Gene ontology analysis for RNA-seq: accounting for selection bias

inferredcites →https://doi.org/10.1186/gb-2010-11-3-r25openalex-snapshot

A scaling normalization method for differential expression analysis of RNA-seq data

inferredcites →https://doi.org/10.1186/gb-2014-15-1-r11openalex-snapshot

dCLIP: a computational approach for comparative CLIP-seq analyses

inferredcites →https://doi.org/10.1186/s12859-017-1934-zopenalex-snapshot

ImageJ2: ImageJ for the next generation of scientific image data

inferredcites →https://doi.org/10.1186/s13024-016-0124-1openalex-snapshot

Predominant expression of Alzheimer’s disease-associated BIN1 in mature oligodendrocytes and localization to white matter tracts

inferredcites →https://doi.org/10.1186/s40478-015-0202-6openalex-snapshot

FUS/TLS deficiency causes behavioral and pathological abnormalities distinct from amyotrophic lateral sclerosis

inferredcites →https://doi.org/10.1261/rna.037804.112openalex-snapshot

FUS regulates genes coding for RNA-binding proteins in neurons by binding to their highly conserved introns

inferredcites →https://doi.org/10.1371/journal.pcbi.1007664openalex-snapshot

Tximeta: Reference sequence checksums for provenance identification in RNA-seq

inferredcites →https://doi.org/10.1371/journal.pone.0004936openalex-snapshot

Transcriptome Analysis of Synaptoneurosomes Identifies Neuroplasticity Genes Overexpressed in Incipient Alzheimer's Disease

inferredcites →https://doi.org/10.1523/jneurosci.0937-07.2007openalex-snapshot

Dysregulated Metabotropic Glutamate Receptor-Dependent Translation of AMPA Receptor and Postsynaptic Density-95 mRNAs at Synapses in a Mouse Model of Fragile X Syndrome

inferredcites →https://doi.org/10.1523/jneurosci.1166-05.2005openalex-snapshot

Evidence for a Significant Role of α3-Containing GABAAReceptors in Mediating the Anxiolytic Effects of Benzodiazepines

inferredcites →https://doi.org/10.1523/jneurosci.18-23-09733.1998openalex-snapshot

The Vesicular GABA Transporter, VGAT, Localizes to Synaptic Vesicles in Sets of Glycinergic as Well as GABAergic Neurons

inferredcites →https://doi.org/10.1523/jneurosci.1866-06.2006openalex-snapshot

Expression and Function of SNAP-25 as a Universal SNARE Component in GABAergic Neurons

inferredcites →https://doi.org/10.1523/jneurosci.2001-11.2011openalex-snapshot

The Residence Time of GABAARs at Inhibitory Synapses Is Determined by Direct Binding of the Receptor α1 Subunit to Gephyrin

inferredcites →https://doi.org/10.1523/jneurosci.2381-12.2013openalex-snapshot

Super-Resolution Imaging Reveals That AMPA Receptors Inside Synapses Are Dynamically Organized in Nanodomains Regulated by PSD95

inferredcites →https://doi.org/10.15252/embj.201592559openalex-snapshot

Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss

inferredcites →https://doi.org/10.1534/g3.119.400185openalex-snapshot

ARMOR: An A utomated R eproducible MO dular Workflow for Preprocessing and Differential Analysis of R NA-seq Data

inferredcites →https://doi.org/10.3389/fncel.2015.00001openalex-snapshot

Disparate roles of zinc in chemical hypoxia-induced neuronal death

inferredcites →https://doi.org/10.3389/fncel.2015.00496openalex-snapshot

Super-Resolution Microscopy Reveals Presynaptic Localization of the ALS/FTD Related Protein FUS in Hippocampal Neurons

inferredcites →https://doi.org/10.3389/fncel.2019.00097openalex-snapshot

Proliferation and Differentiation in the Adult Subventricular Zone Are Not Affected by CSF1R Inhibition

inferredcites →https://doi.org/10.3389/fncel.2019.00256openalex-snapshot

Synaptic FUS Localization During Motoneuron Development and Its Accumulation in Human ALS Synapses

inferredcites →https://doi.org/10.3389/fnmol.2019.00152openalex-snapshot

Posttranscriptional Gene Regulation of the GABA Receptor to Control Neuronal Inhibition

inferredcites →https://doi.org/10.3389/fnmol.2019.00154openalex-snapshot

Molecular Specialization of GABAergic Synapses on the Soma and Axon in Cortical and Hippocampal Circuit Function and Dysfunction

inferredcites →https://doi.org/10.3390/cells9020313openalex-snapshot

Proteomic Analysis of Brain Region and Sex-Specific Synaptic Protein Expression in the Adult Mouse Brain

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/978-1-0716-1975-9_19openalex-snapshot

Identification of RNA–RBP Interactions in Subcellular Compartments by CLIP-Seq

inferred← citeshttps://doi.org/10.1016/j.devcel.2020.09.014openalex-snapshot

Phase Separation and Neurodegenerative Diseases: A Disturbance in the Force

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