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http://purl.uniprot.org/citations/26456651http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/26456651http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/26456651http://www.w3.org/2000/01/rdf-schema#comment"Nuclear VCP-like 2 (NVL2) is a chaperone-like nucleolar ATPase of the AAA (ATPase associated with diverse cellular activities) family, which exhibits a high level of amino acid sequence similarity with the cytosolic AAA-ATPase VCP/p97. These proteins generally act on macromolecular complexes to stimulate energy-dependent release of their constituents. We previously showed that NVL2 interacts with RNA processing/degradation machinery containing an RNA helicase MTR4/DOB1 and an exonuclease complex, nuclear exosome, and involved in the biogenesis of 60S ribosomal subunits. These observations implicate NVL2 as a remodeling factor for the MTR4-exosome complex during the maturation of pre-ribosomal particles. Here, we used a proteomic screen and identified a WD repeat-containing protein 74 (WDR74) as a factor that specifically dissociates from this complex depending on the ATPase activity of NVL2. WDR74 shows weak amino acid sequence similarity with the yeast ribosome biogenesis protein Nsa1 and is co-localized with NVL2 in the nucleolus. Knockdown of WDR74 decreases 60S ribosome levels. Taken together, our results suggest that WDR74 is a novel regulatory protein of the MTR4-exsosome complex whose interaction is regulated by NVL2 and is involved in ribosome biogenesis."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.org/dc/terms/identifier"doi:10.1016/j.bbrc.2015.09.160"xsd:string
http://purl.uniprot.org/citations/26456651http://purl.org/dc/terms/identifier"doi:10.1016/j.bbrc.2015.09.160"xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/author"Ishida Y."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/author"Ishida Y."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/author"Nagahama M."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/author"Nagahama M."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/author"Hiraishi N."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/author"Hiraishi N."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/name"Biochem. Biophys. Res. Commun."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/name"Biochem. Biophys. Res. Commun."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/pages"534-540"xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/pages"534-540"xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/title"AAA-ATPase NVL2 acts on MTR4-exosome complex to dissociate the nucleolar protein WDR74."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/title"AAA-ATPase NVL2 acts on MTR4-exosome complex to dissociate the nucleolar protein WDR74."xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/volume"467"xsd:string
http://purl.uniprot.org/citations/26456651http://purl.uniprot.org/core/volume"467"xsd:string
http://purl.uniprot.org/citations/26456651http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/26456651
http://purl.uniprot.org/citations/26456651http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/26456651
http://purl.uniprot.org/citations/26456651http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/26456651
http://purl.uniprot.org/citations/26456651http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/26456651