ABSTRACT
Rett Syndrome is a neurological disorder caused by mutations in the gene encoding methyl CpG binding protein 2 (MeCP2) and characterized by severe intellectual disability. The cholinergic system is a critical modulator of cognitive ability and is affected in patients with Rett Syndrome. To better understand the importance of MeCP2 function in cholinergic neurons, we studied the effect of selective Mecp2 deletion from cholinergic neurons in mice. Mice with Mecp2 deletion from cholinergic neurons were selectively impaired in assays of recognition memory, a cognitive task largely mediated by the perirhinal cortex (PRH). Deletion of Mecp2 from cholinergic neurons resulted in profound alterations in baseline firing of L5/6 neurons and eliminated the responses of these neurons to optogenetic stimulation of cholinergic input to PRH. Both the behavioral and the electrophysiological deficits of cholinergic Mecp2 deletion were rescued by inhibiting ACh breakdown with donepezil treatment.
Subject(s)
Cholinergic Neurons/metabolism , Methyl-CpG-Binding Protein 2/metabolism , Perirhinal Cortex/metabolism , Recognition, Psychology/physiology , Action Potentials/drug effects , Action Potentials/physiology , Animals , Cholinergic Neurons/drug effects , Cholinesterase Inhibitors/pharmacology , Disease Models, Animal , Donepezil/pharmacology , Methyl-CpG-Binding Protein 2/genetics , Mice , Mice, Knockout , Optogenetics , Perirhinal Cortex/drug effects , Phenotype , Recognition, Psychology/drug effects , Rett Syndrome/genetics , Rett Syndrome/metabolismABSTRACT
RNA splicing entails the coordinated interaction of more than 150 proteins in the spliceosome, one of the most complex of the cell's molecular machines. We previously discovered that the RNA-binding motif protein 17 (RBM17), a component of the spliceosome, is essential for survival and cell maintenance. Here, we find that it interacts with the spliceosomal factors U2SURP and CHERP and that they reciprocally regulate each other's stability, both in mouse and in human cells. Individual knockdown of each of the three proteins induces overlapping changes in splicing and gene expression of transcripts enriched for RNA-processing factors. Our results elucidate the function of RBM17, U2SURP, and CHERP and link the activity of the spliceosome to the regulation of downstream RNA-binding proteins. These data support the hypothesis that, beyond driving constitutive splicing, spliceosomal factors can regulate alternative splicing of specific targets.
Subject(s)
DNA-Binding Proteins/metabolism , Gene Expression Regulation , Membrane Proteins/metabolism , Nerve Tissue Proteins/physiology , RNA Splicing Factors/metabolism , RNA Splicing , RNA-Binding Proteins/metabolism , Animals , CRISPR-Cas Systems , DNA-Binding Proteins/antagonists & inhibitors , DNA-Binding Proteins/genetics , Female , HEK293 Cells , Humans , Male , Membrane Proteins/antagonists & inhibitors , Membrane Proteins/genetics , Mice , Mice, Inbred C57BL , Mice, Knockout , RNA Splicing Factors/antagonists & inhibitors , RNA Splicing Factors/genetics , RNA Splicing Factors/physiology , RNA-Binding Proteins/antagonists & inhibitors , RNA-Binding Proteins/genetics , SpliceosomesABSTRACT
Splicing regulation is an important step of post-transcriptional gene regulation. It is a highly dynamic process orchestrated by RNA-binding proteins (RBPs). RBP dysfunction and global splicing dysregulation have been implicated in many human diseases, but the in vivo functions of most RBPs and the splicing outcome upon their loss remain largely unexplored. Here we report that constitutive deletion of Rbm17, which encodes an RBP with a putative role in splicing, causes early embryonic lethality in mice and that its loss in Purkinje neurons leads to rapid degeneration. Transcriptome profiling of Rbm17-deficient and control neurons and subsequent splicing analyses using CrypSplice, a new computational method that we developed, revealed that more than half of RBM17-dependent splicing changes are cryptic. Importantly, RBM17 represses cryptic splicing of genes that likely contribute to motor coordination and cell survival. This finding prompted us to re-analyze published datasets from a recent report on TDP-43, an RBP implicated in amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), as it was demonstrated that TDP-43 represses cryptic exon splicing to promote cell survival. We uncovered a large number of TDP-43-dependent splicing defects that were not previously discovered, revealing that TDP-43 extensively regulates cryptic splicing. Moreover, we found a significant overlap in genes that undergo both RBM17- and TDP-43-dependent cryptic splicing repression, many of which are associated with survival. We propose that repression of cryptic splicing by RBPs is critical for neuronal health and survival. CrypSplice is available at www.liuzlab.org/CrypSplice.
Subject(s)
Amyotrophic Lateral Sclerosis/genetics , DNA-Binding Proteins/genetics , Frontotemporal Dementia/genetics , Nerve Degeneration/genetics , Nerve Tissue Proteins/genetics , RNA Splicing Factors/genetics , Amyotrophic Lateral Sclerosis/physiopathology , Animals , Computational Biology/methods , Disease Models, Animal , Exons/genetics , Frontotemporal Dementia/physiopathology , Gene Expression Regulation, Developmental , Humans , Mice , Nerve Degeneration/pathology , Nerve Tissue Proteins/biosynthesis , Purkinje Cells/metabolism , Purkinje Cells/pathology , RNA Splicing/genetics , RNA Splicing Factors/biosynthesis , RNA-Binding Proteins/biosynthesis , RNA-Binding Proteins/geneticsABSTRACT
Many neurodegenerative proteinopathies share a common pathogenic mechanism: the abnormal accumulation of disease-related proteins. As growing evidence indicates that reducing the steady-state levels of disease-causing proteins mitigates neurodegeneration in animal models, we developed a strategy to screen for genes that decrease the levels of tau, whose accumulation contributes to the pathology of both Alzheimer disease (AD) and progressive supranuclear palsy (PSP). Integrating parallel cell-based and Drosophila genetic screens, we discovered that tau levels are regulated by Nuak1, an AMPK-related kinase. Nuak1 stabilizes tau by phosphorylation specifically at Ser356. Inhibition of Nuak1 in fruit flies suppressed neurodegeneration in tau-expressing Drosophila, and Nuak1 haploinsufficiency rescued the phenotypes of a tauopathy mouse model. These results demonstrate that decreasing total tau levels is a valid strategy for mitigating tau-related neurodegeneration and reveal Nuak1 to be a novel therapeutic entry point for tauopathies.
Subject(s)
Behavior, Animal , Protein Kinases/genetics , Repressor Proteins/genetics , Tauopathies/genetics , tau Proteins/metabolism , Alzheimer Disease/genetics , Animals , Cell Line, Tumor , Conditioning, Psychological , Disease Models, Animal , Drosophila , Fear , Fluorescent Antibody Technique , Humans , Immunoblotting , Mice , Phosphorylation/genetics , Supranuclear Palsy, Progressive/geneticsABSTRACT
Several neurodegenerative diseases are driven by the toxic gain-of-function of specific proteins within the brain. Elevated levels of alpha-synuclein (α-Syn) appear to drive neurotoxicity in Parkinson's disease (PD); neuronal accumulation of tau is a hallmark of Alzheimer's disease (AD); and their increased levels cause neurodegeneration in humans and model organisms. Despite the clinical differences between AD and PD, several lines of evidence suggest that α-Syn and tau overlap pathologically. The connections between α-Syn and tau led us to ask whether these proteins might be regulated through a shared pathway. We therefore screened for genes that affect post-translational levels of α-Syn and tau. We found that TRIM28 regulates α-Syn and tau levels and that its reduction rescues toxicity in animal models of tau- and α-Syn-mediated degeneration. TRIM28 stabilizes and promotes the nuclear accumulation and toxicity of both proteins. Intersecting screens across comorbid proteinopathies thus reveal shared mechanisms and therapeutic entry points.
Subject(s)
Cell Nucleus/metabolism , Tripartite Motif-Containing Protein 28/metabolism , alpha-Synuclein/metabolism , tau Proteins/metabolism , Alzheimer Disease/physiopathology , Animals , Cells, Cultured , Disease Models, Animal , Humans , Mice , Parkinson Disease/physiopathologyABSTRACT
Spinocerebellar ataxia type 1 (SCA1) is a paradigmatic neurodegenerative proteinopathy, in which a mutant protein (in this case, ATAXIN1) accumulates in neurons and exerts toxicity; in SCA1, this process causes progressive deterioration of motor coordination. Seeking to understand how post-translational modification of ATAXIN1 levels influences disease, we discovered that the RNA-binding protein PUMILIO1 (PUM1) not only directly regulates ATAXIN1 but also plays an unexpectedly important role in neuronal function. Loss of Pum1 caused progressive motor dysfunction and SCA1-like neurodegeneration with motor impairment, primarily by increasing Ataxin1 levels. Breeding Pum1(+/-) mice to SCA1 mice (Atxn1(154Q/+)) exacerbated disease progression, whereas breeding them to Atxn1(+/-) mice normalized Ataxin1 levels and largely rescued the Pum1(+/-) phenotype. Thus, both increased wild-type ATAXIN1 levels and PUM1 haploinsufficiency could contribute to human neurodegeneration. These results demonstrate the importance of studying post-transcriptional regulation of disease-driving proteins to reveal factors underlying neurodegenerative disease.
Subject(s)
Nerve Tissue Proteins/genetics , Neurodegenerative Diseases/genetics , Nuclear Proteins/genetics , RNA-Binding Proteins/genetics , 3' Untranslated Regions , Animals , Antigens, Ly/genetics , Ataxin-1 , Ataxins , Brain/metabolism , Gene Knock-In Techniques , Haploinsufficiency , Humans , Membrane Proteins/genetics , Mice , Mice, Knockout , MicroRNAs/metabolism , Mutation , Neurodegenerative Diseases/pathology , Nucleic Acid Conformation , RNA Processing, Post-Transcriptional , RNA Stability , RNA, Messenger/chemistryABSTRACT
During corticogenesis, late-born callosal projection neurons (CPNs) acquire their laminar position through glia-guided radial migration and then undergo final differentiation. However, the mechanisms controlling radial migration and final morphology of CPNs are poorly defined. Here, we show that in COUP-TFI mutant mice CPNs are correctly specified, but are delayed in reaching the cortical plate and have morphological defects during migration. Interestingly, we observed that the rate of neuronal migration to the cortical plate normally follows a low-rostral to high-caudal gradient, similar to that described for COUP-TFI. This gradient is strongly impaired in COUP-TFI(-/-) brains. Moreover, the expression of the Rho-GTPase Rnd2, a modulator of radial migration, is complementary to both these gradients and strongly increases in the absence of COUP-TFI function. We show that COUP-TFI directly represses Rnd2 expression at the post-mitotic level along the rostrocaudal axis of the neocortex. Restoring correct Rnd2 levels in COUP-TFI(-/-) brains cell-autonomously rescues neuron radial migration and morphological transitions. We also observed impairments in axonal elongation and dendritic arborization of COUP-TFI-deficient CPNs, which were rescued by lowering Rnd2 expression levels. Thus, our data demonstrate that COUP-TFI modulates late-born neuron migration and favours proper differentiation of CPNs by finely regulating Rnd2 expression levels.