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http://purl.uniprot.org/citations/16086026http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16086026http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16086026http://www.w3.org/2000/01/rdf-schema#comment"Eukaryotic cells coordinately regulate histone and DNA synthesis. In mammalian cells, most of the regulation of histone synthesis occurs post-transcriptionally by regulating the concentrations of histone mRNA. As cells enter S phase, histone mRNA levels increase, and at the end of S phase they are rapidly degraded. Moreover, inhibition of DNA synthesis causes rapid degradation of histone mRNAs. Replication-dependent histone mRNAs are the only metazoan mRNAs that are not polyadenylated. Instead, they end with a conserved stem-loop structure, which is the only cis-acting element required for coupling regulation of histone mRNA half-life with DNA synthesis. Here we show that regulated degradation of histone mRNAs requires Upf1, a key regulator of the nonsense-mediated decay pathway, and ATR, a key regulator of the DNA damage checkpoint pathway activated during replication stress."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.org/dc/terms/identifier"doi:10.1038/nsmb972"xsd:string
http://purl.uniprot.org/citations/16086026http://purl.org/dc/terms/identifier"doi:10.1038/nsmb972"xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/author"Kaygun H."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/author"Kaygun H."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/author"Marzluff W.F."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/author"Marzluff W.F."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/name"Nat. Struct. Mol. Biol."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/name"Nat. Struct. Mol. Biol."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/pages"794-800"xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/pages"794-800"xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/title"Regulated degradation of replication-dependent histone mRNAs requires both ATR and Upf1."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/title"Regulated degradation of replication-dependent histone mRNAs requires both ATR and Upf1."xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/volume"12"xsd:string
http://purl.uniprot.org/citations/16086026http://purl.uniprot.org/core/volume"12"xsd:string
http://purl.uniprot.org/citations/16086026http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16086026
http://purl.uniprot.org/citations/16086026http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16086026
http://purl.uniprot.org/citations/16086026http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16086026
http://purl.uniprot.org/citations/16086026http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16086026
http://purl.uniprot.org/uniprot/Q13315http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/16086026
http://purl.uniprot.org/uniprot/Q92900http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/16086026