<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Antony C</submitter><funding>NICHD NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>3826-3839.e9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9588704</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>82(20)</volume><pubmed_abstract>Ribosomal RNAs (rRNAs) are the most abundant cellular RNAs, and their synthesis from rDNA repeats by RNA polymerase I accounts for the bulk of all transcription. Despite substantial variation in rRNA transcription rates across cell types, little is known about cell-type-specific factors that bind rDNA and regulate rRNA transcription to meet tissue-specific needs. Using hematopoiesis as a model system, we mapped about 2,200 ChIP-seq datasets for 250 transcription factors (TFs) and chromatin proteins to human and mouse rDNA and identified robust binding of multiple TF families to canonical TF motifs on rDNA. Using a 47S-FISH-Flow assay developed for nascent rRNA quantification, we demonstrated that targeted degradation of C/EBP alpha (CEBPA), a critical hematopoietic TF with conserved rDNA b</pubmed_abstract><journal>Molecular cell</journal><pubmed_title>Control of ribosomal RNA synthesis by hematopoietic transcription factors.</pubmed_title><pmcid>PMC9588704</pmcid><funding_grant_id>R01 HD089245</funding_grant_id><funding_grant_id>R35 GM119735</funding_grant_id><funding_grant_id>R01 HL155144</funding_grant_id><funding_grant_id>U01 CA226187</funding_grant_id><funding_grant_id>R35 GM138035</funding_grant_id><pubmed_authors>Moss T</pubmed_authors><pubmed_authors>Tan K</pubmed_authors><pubmed_authors>Wu-Corts DJ</pubmed_authors><pubmed_authors>Blum J</pubmed_authors><pubmed_authors>George SS</pubmed_authors><pubmed_authors>Wilusz JE</pubmed_authors><pubmed_authors>Pimkin M</pubmed_authors><pubmed_authors>Tremblay MG</pubmed_authors><pubmed_authors>Thorsheim CL</pubmed_authors><pubmed_authors>Antony C</pubmed_authors><pubmed_authors>Lv K</pubmed_authors><pubmed_authors>Paralkar VR</pubmed_authors><pubmed_authors>Gao L</pubmed_authors><pubmed_authors>Ai Y</pubmed_authors><pubmed_authors>Somers P</pubmed_authors><pubmed_authors>Ganley ARD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Control of ribosomal RNA synthesis by hematopoietic transcription factors.</name><description>Ribosomal RNAs (rRNAs) are the most abundant cellular RNAs, and their synthesis from rDNA repeats by RNA polymerase I accounts for the bulk of all transcription. Despite substantial variation in rRNA transcription rates across cell types, little is known about cell-type-specific factors that bind rDNA and regulate rRNA transcription to meet tissue-specific needs. Using hematopoiesis as a model system, we mapped about 2,200 ChIP-seq datasets for 250 transcription factors (TFs) and chromatin proteins to human and mouse rDNA and identified robust binding of multiple TF families to canonical TF motifs on rDNA. Using a 47S-FISH-Flow assay developed for nascent rRNA quantification, we demonstrated that targeted degradation of C/EBP alpha (CEBPA), a critical hematopoietic TF with conserved rDNA b</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-28T01:39:36.15Z</modification><creation>2025-02-19T03:06:21.33Z</creation></dates><accession>S-EPMC9588704</accession><cross_references><pubmed>36113481</pubmed><doi>10.1016/j.molcel.2022.08.027</doi></cross_references></HashMap>