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1.
Nucleic Acids Res ; 51(7): 3357-3374, 2023 04 24.
Article in English | MEDLINE | ID: mdl-36869663

ABSTRACT

The conserved H/ACA RNPs consist of one H/ACA RNA and 4 core proteins: dyskerin, NHP2, NOP10, and GAR1. Its assembly requires several assembly factors. A pre-particle containing the nascent RNAs, dyskerin, NOP10, NHP2 and NAF1 is assembled co-transcriptionally. NAF1 is later replaced by GAR1 to form mature RNPs. In this study, we explore the mechanism leading to the assembly of H/ACA RNPs. We performed the analysis of GAR1, NHP2, SHQ1 and NAF1 proteomes by quantitative SILAC proteomic, and analyzed purified complexes containing these proteins by sedimentation on glycerol gradient. We propose the formation of several distinct intermediate complexes during H/ACA RNP assembly, notably the formation of early protein-only complexes containing at least the core proteins dyskerin, NOP10, and NHP2, and the assembly factors SHQ1 and NAF1. We also identified new proteins associated with GAR1, NHP2, SHQ1 and NAF1, which can be important for box H/ACA assembly or function. Moreover, even though GAR1 is regulated by methylations, the nature, localization, and functions of these methylations are not well known. Our MS analysis of purified GAR1 revealed new sites of arginine methylations. Additionally, we showed that unmethylated GAR1 is correctly incorporated in H/ACA RNPs, even though with less efficiency than methylated ones.


Subject(s)
Proteomics , Ribonucleoproteins , Ribonucleoproteins/genetics , Ribonucleoproteins, Small Nucleolar/genetics , Ribonucleoproteins, Small Nucleolar/metabolism , RNA-Binding Proteins , RNA/genetics
2.
Nucleic Acids Res ; 45(9): 5399-5413, 2017 May 19.
Article in English | MEDLINE | ID: mdl-28115638

ABSTRACT

Selenoprotein synthesis requires the co-translational recoding of a UGASec codon. This process involves an RNA structural element, called Selenocysteine Insertion Sequence (SECIS) and the SECIS binding protein 2 (SBP2). Several selenoprotein mRNAs undergo unusual cap hypermethylation by the trimethylguanosine synthase 1 (Tgs1), which is recruited by the ubiquitous Survival of MotoNeurons (SMN) protein. SMN, the protein involved in spinal muscular atrophy, is part of a chaperone complex that collaborates with the methylosome for RNP assembly. Here, we analyze the role of individual SMN and methylosome components in selenoprotein mRNP assembly and translation. We show that SBP2 interacts directly with four proteins of the SMN complex and the methylosome core proteins. Nevertheless, SBP2 is not a methylation substrate of the methylosome. We found that both SMN and methylosome complexes are required for efficient translation of the selenoprotein GPx1 in vivo. We establish that the steady-state level of several selenoprotein mRNAs, major regulators of oxidative stress damage in neurons, is specifically reduced in the spinal cord of SMN-deficient mice and that cap hypermethylation of GPx1 mRNA is affected. Altogether we identified a new function of the SMN complex and the methylosome in selenoprotein mRNP assembly and expression.


Subject(s)
Protein Biosynthesis , RNA-Binding Proteins/metabolism , Ribonucleoproteins/metabolism , SMN Complex Proteins/metabolism , Selenoproteins/metabolism , Glutathione Peroxidase , HEK293 Cells , HeLa Cells , Humans , Methylation , Models, Biological , Muscular Atrophy, Spinal/metabolism , Muscular Atrophy, Spinal/pathology , Protein Binding , Spinal Cord/metabolism , Glutathione Peroxidase GPX1
3.
Nucleic Acids Res ; 43(18): 8973-89, 2015 Oct 15.
Article in English | MEDLINE | ID: mdl-26275778

ABSTRACT

The Sm proteins are loaded on snRNAs by the SMN complex, but how snRNP-specific proteins are assembled remains poorly characterized. U4 snRNP and box C/D snoRNPs have structural similarities. They both contain the 15.5K and proteins with NOP domains (PRP31 for U4, NOP56/58 for snoRNPs). Biogenesis of box C/D snoRNPs involves NUFIP and the HSP90/R2TP chaperone system and here, we explore the function of this machinery in U4 RNP assembly. We show that yeast Prp31 interacts with several components of the NUFIP/R2TP machinery, and that these interactions are separable from each other. In human cells, PRP31 mutants that fail to stably associate with U4 snRNA still interact with components of the NUFIP/R2TP system, indicating that these interactions precede binding of PRP31 to U4 snRNA. Knock-down of NUFIP leads to mislocalization of PRP31 and decreased association with U4. Moreover, NUFIP is associated with the SMN complex through direct interactions with Gemin3 and Gemin6. Altogether, our data suggest a model in which the NUFIP/R2TP system is connected with the SMN complex and facilitates assembly of U4 snRNP-specific proteins.


Subject(s)
Eye Proteins/metabolism , Molecular Chaperones/metabolism , Ribonucleoprotein, U4-U6 Small Nuclear/metabolism , Ribosomal Proteins/metabolism , SMN Complex Proteins/metabolism , Saccharomyces cerevisiae Proteins/metabolism , Spliceosomes/metabolism , Cell Line , Coiled Bodies/metabolism , Cytoplasm/metabolism , Eye Proteins/chemistry , Eye Proteins/genetics , HeLa Cells , Humans , Mutagenesis, Insertional , RNA, Small Nuclear/metabolism , Ribonucleoproteins, Small Nuclear/metabolism , Ribonucleoproteins, Small Nucleolar/metabolism , Saccharomyces cerevisiae Proteins/genetics , Spliceosomes/genetics
4.
PLoS Pathog ; 11(4): e1004859, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25923687

ABSTRACT

It is well established that persistent viral infection may impair cellular function of specialized cells without overt damage. This concept, when applied to neurotropic viruses, may help to understand certain neurologic and neuropsychiatric diseases. Borna disease virus (BDV) is an excellent example of a persistent virus that targets the brain, impairs neural functions without cell lysis, and ultimately results in neurobehavioral disturbances. Recently, we have shown that BDV infects human neural progenitor cells (hNPCs) and impairs neurogenesis, revealing a new mechanism by which BDV may interfere with brain function. Here, we sought to identify the viral proteins and molecular pathways that are involved. Using lentiviral vectors for expression of the bdv-p and bdv-x viral genes, we demonstrate that the phosphoprotein P, but not the X protein, diminishes human neurogenesis and, more particularly, GABAergic neurogenesis. We further reveal a decrease in pro-neuronal factors known to be involved in neuronal differentiation (ApoE, Noggin, TH and Scg10/Stathmin2), demonstrating that cellular dysfunction is associated with impairment of specific components of the molecular program that controls neurogenesis. Our findings thus provide the first evidence that a viral protein impairs GABAergic human neurogenesis, a process that is dysregulated in several neuropsychiatric disorders. They improve our understanding of the mechanisms by which a persistent virus may interfere with brain development and function in the adult.


Subject(s)
Borna disease virus/physiology , Down-Regulation , GABAergic Neurons/metabolism , Host-Pathogen Interactions , Neurogenesis , Phosphoproteins/metabolism , Viral Structural Proteins/metabolism , Active Transport, Cell Nucleus , Apolipoproteins E/antagonists & inhibitors , Apolipoproteins E/metabolism , Biomarkers/chemistry , Biomarkers/metabolism , Borna Disease/metabolism , Borna Disease/pathology , Borna Disease/virology , Carrier Proteins/antagonists & inhibitors , Carrier Proteins/metabolism , Cell Proliferation , Cells, Cultured , France , GABAergic Neurons/cytology , GABAergic Neurons/pathology , GABAergic Neurons/virology , Human Embryonic Stem Cells/cytology , Human Embryonic Stem Cells/metabolism , Human Embryonic Stem Cells/pathology , Human Embryonic Stem Cells/virology , Humans , Membrane Proteins/antagonists & inhibitors , Membrane Proteins/metabolism , Nerve Tissue Proteins/antagonists & inhibitors , Nerve Tissue Proteins/metabolism , Phosphoproteins/genetics , Recombinant Proteins/metabolism , Recombinant Proteins/toxicity , Stathmin , Tyrosine 3-Monooxygenase/antagonists & inhibitors , Tyrosine 3-Monooxygenase/metabolism , Viral Structural Proteins/genetics
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