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dc.contributor.authorBelk, Jonathan Philip
dc.contributor.authorHe, Feng
dc.contributor.authorJacobson, Allan
dc.date2022-08-11T08:09:02.000
dc.date.accessioned2022-08-23T16:16:15Z
dc.date.available2022-08-23T16:16:15Z
dc.date.issued1999-08-13
dc.date.submitted2008-07-16
dc.identifier.citation<p>RNA. 1999 Aug;5(8):1055-70.</p>
dc.identifier.issn1355-8382 (Print)
dc.identifier.pmid10445880
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34287
dc.description.abstractThe yeast NMD3 gene was identified in a two-hybrid screen using the nonsense-mediated mRNA decay factor, Upf1p, as bait. NMD3 was shown to encode an essential, highly conserved protein that associated principally with free 60S ribosomal subunits. Overexpression of a truncated form of Nmd3p, lacking 100 C-terminal amino acids and most of its Upf1p-interacting domain, had dominant-negative effects on both cell growth and protein synthesis and promoted the formation of polyribosome half-mers. These effects were eliminated by truncation of an additional 100 amino acids from Nmd3p. Overexpression of the nmd3delta100 allele also led to increased synthesis and destabilization of some ribosomal protein mRNAs, and increased synthesis and altered processing of 35S pre-rRNA. Our data suggest that Nmd3p has a role in the formation, function, or maintenance of the 60S ribosomal subunit and may provide a link for Upf1p to 80S monosomes.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=10445880&dopt=Abstract ">Link to article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1369829/
dc.subjectAmino Acid Sequence; Blotting, Northern; Cell Division; Cloning, Molecular; Fungal Proteins; Galactose; Gene Expression Regulation, Fungal; Genes, Dominant; Models, Genetic; Molecular Sequence Data; Polyribosomes; Protein Biosynthesis; Protein Synthesis Inhibitors; RNA Helicases; RNA, Messenger; RNA, Ribosomal; *RNA-Binding Proteins; Saccharomyces cerevisiae; *Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Time Factors
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleOverexpression of truncated Nmd3p inhibits protein synthesis in yeast
dc.typeJournal Article
dc.source.journaltitleRNA (New York, N.Y.)
dc.source.volume5
dc.source.issue8
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/94
dc.identifier.contextkey549656
html.description.abstract<p>The yeast NMD3 gene was identified in a two-hybrid screen using the nonsense-mediated mRNA decay factor, Upf1p, as bait. NMD3 was shown to encode an essential, highly conserved protein that associated principally with free 60S ribosomal subunits. Overexpression of a truncated form of Nmd3p, lacking 100 C-terminal amino acids and most of its Upf1p-interacting domain, had dominant-negative effects on both cell growth and protein synthesis and promoted the formation of polyribosome half-mers. These effects were eliminated by truncation of an additional 100 amino acids from Nmd3p. Overexpression of the nmd3delta100 allele also led to increased synthesis and destabilization of some ribosomal protein mRNAs, and increased synthesis and altered processing of 35S pre-rRNA. Our data suggest that Nmd3p has a role in the formation, function, or maintenance of the 60S ribosomal subunit and may provide a link for Upf1p to 80S monosomes.</p>
dc.identifier.submissionpathgsbs_sp/94
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages1055-70


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