4.5 Article

Identification of DHX33 as a Mediator of rRNA Synthesis and Cell Growth

Journal

MOLECULAR AND CELLULAR BIOLOGY
Volume 31, Issue 23, Pages 4676-4691

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.05832-11

Keywords

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Funding

  1. NIH [5T32 GM007067, CA120436]
  2. Department of Defense [X81XWH-08-BCRP-PREDOC]
  3. Era of Hope scholar award in breast cancer research [BC007304]

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In this report, we employed a lentiviral RNA interference screen to discover nucleolar DEAD/DEAH-box helicases involved in RNA polymerase I (Pol I)-mediated transcriptional activity. Our screen identified DHX33 as an important modulator of 47S rRNA transcription. We show that DHX33 is a cell cycle-regulated nucleolar protein that associates with ribosomal DNA (rDNA) loci, where it interacts with the RNA Pol I transcription factor upstream binding factor (UBF). DHX33 knockdown decreased the association of Pol I with rDNA and caused a dramatic decrease in levels of rRNA synthesis. Wild-type DHX33 overexpression, but not a DNA binding-defective mutant, enhanced 47S rRNA synthesis by promoting the association of RNA polymerase I with rDNA loci. In addition, an NTPase-defective DHX33 mutant (K94R) acted as a dominant negative mutant, inhibiting endogenous rRNA synthesis. Moreover, DHX33 deficiency in primary human fibroblasts triggered a nucleolar p53 stress response, resulting in an attenuation of proliferation. Thus, we show the mechanistic importance of DHX33 in rRNA transcription and proliferation.

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