Journal article
C-MYC coordinately regulates ribosomal gene chromatin remodeling and Pol i availability during granulocyte differentiation
G Poortinga, M Wall, E Sanij, K Siwicki, J Ellul, D Brown, TP Holloway, RD Hannan, GA McArthur
Nucleic Acids Research | Published : 2011
DOI: 10.1093/nar/gkq1205
Abstract
Loss of c-MYC is required for downregulation of ribosomal RNA (rRNA) gene (rDNA) transcription by RNA Polymerase I (Pol I) during granulocyte differentiation. Here, we demonstrate a robust reduction of Pol I loading onto rDNA that along with a depletion of the MYC target gene upstream binding factor (UBF) and a switch from epigenetically active to silent rDNA accompanies this MYC reduction. We hypothesized that MYC may coordinate these mechanisms via direct regulation of multiple components of the Pol I transcription apparatus. Using gene expression arrays we identified a 'regulon' of Pol I factors that are both downregulated during differentiation and reinduced in differentiated granulocyte..
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Grants
Awarded by National Health and Medical Research Council
Funding Acknowledgements
National Health and Medical Research Council (NHMRC) of Australia (project grants 509088, 508907 to R. D. H. and 400120, 566876 to G.A.M.); NHMRC Research Fellowship (166908 to R.D.H.); Cancer Council of Victoria Sir Edward Weary Dunlop Clinical Research Fellowship (to G.A.M.). Funding for open access charge: NHMRC.