<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Prieto JL</submitter><funding>Medical Research Council</funding><pagination>2041-54</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1948859</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(16)</volume><pubmed_abstract>Efficient ribosome biogenesis requires coordination of a highly complex series of events. Early events include pre-RNA transcription, processing, and modification. Analysis in yeast has demonstrated that t-UTPs, components of the U3 snoRNA-containing pre-rRNA processing complex, are required for efficient transcription of ribosomal genes (rDNA) by RNA polymerase I (pol I). Here, we characterize human t-UTPs and establish that their ability to link transcription and pre-rRNA processing is evolutionarily conserved. The pol I transcription factor UBF binds extensively across rDNA throughout the cell cycle, resulting in a specialized form of chromatin that is the hallmark of active nucleolar organizer regions (NORs). Transcriptionally silent pseudo-NORs are ectopic, chromosomally integrated, artificial arrays that mimic this specialized chromatin structure. Pseudo-NORs sequester t-UTPs and factors linking transcription with pre-rRNA modification (Nopp140 and Treacle). Recruitment is independent of transcription, the underlying DNA sequence, and location within the nucleolus. Previously, we have demonstrated that pseudo-NORs sequester every component of the pol I transcription machinery. Taken together, these results highlight the importance of the specialized chromatin structure at active NORs in coordinating early events in ribosome biogenesis and nucleolar formation.</pubmed_abstract><journal>Genes &amp; development</journal><pubmed_title>Recruitment of factors linking transcription and processing of pre-rRNA to NOR chromatin is UBF-dependent and occurs independent of transcription in human cells.</pubmed_title><pmcid>PMC1948859</pmcid><funding_grant_id>G0500323</funding_grant_id><pubmed_authors>McStay B</pubmed_authors><pubmed_authors>Prieto JL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Recruitment of factors linking transcription and processing of pre-rRNA to NOR chromatin is UBF-dependent and occurs independent of transcription in human cells.</name><description>Efficient ribosome biogenesis requires coordination of a highly complex series of events. Early events include pre-RNA transcription, processing, and modification. Analysis in yeast has demonstrated that t-UTPs, components of the U3 snoRNA-containing pre-rRNA processing complex, are required for efficient transcription of ribosomal genes (rDNA) by RNA polymerase I (pol I). Here, we characterize human t-UTPs and establish that their ability to link transcription and pre-rRNA processing is evolutionarily conserved. The pol I transcription factor UBF binds extensively across rDNA throughout the cell cycle, resulting in a specialized form of chromatin that is the hallmark of active nucleolar organizer regions (NORs). Transcriptionally silent pseudo-NORs are ectopic, chromosomally integrated, artificial arrays that mimic this specialized chromatin structure. Pseudo-NORs sequester t-UTPs and factors linking transcription with pre-rRNA modification (Nopp140 and Treacle). Recruitment is independent of transcription, the underlying DNA sequence, and location within the nucleolus. Previously, we have demonstrated that pseudo-NORs sequester every component of the pol I transcription machinery. Taken together, these results highlight the importance of the specialized chromatin structure at active NORs in coordinating early events in ribosome biogenesis and nucleolar formation.</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Aug</publication><modification>2024-11-07T05:21:02.456Z</modification><creation>2019-06-06T14:53:28Z</creation></dates><accession>S-EPMC1948859</accession><cross_references><pubmed>17699751</pubmed><doi>10.1101/gad.436707</doi></cross_references></HashMap>