RNA-interference screen for p53 regulators unveils a role of WDR75 in ribosome biogenesis
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
34611297
PubMed Central
PMC8901908
DOI
10.1038/s41418-021-00882-0
PII: 10.1038/s41418-021-00882-0
Knihovny.cz E-zdroje
- MeSH
- buněčné jadérko genetika metabolismus MeSH
- DEAD-box RNA-helikasy metabolismus MeSH
- jaderné proteiny genetika metabolismus MeSH
- lidé MeSH
- molekuly buněčné adheze metabolismus MeSH
- nádorové buněčné linie MeSH
- nádorový supresorový protein p53 genetika metabolismus MeSH
- prekurzory RNA metabolismus MeSH
- ribozomální proteiny * genetika metabolismus MeSH
- ribozomy genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- BYSL protein, human MeSH Prohlížeč
- DDX56 protein, human MeSH Prohlížeč
- DEAD-box RNA-helikasy MeSH
- jaderné proteiny MeSH
- molekuly buněčné adheze MeSH
- nádorový supresorový protein p53 MeSH
- prekurzory RNA MeSH
- ribozomální proteiny * MeSH
- TP53 protein, human MeSH Prohlížeč
Ribosome biogenesis is an essential, energy demanding process whose deregulation has been implicated in cancer, aging, and neurodegeneration. Ribosome biogenesis is therefore under surveillance of pathways including the p53 tumor suppressor. Here, we first performed a high-content siRNA-based screen of 175 human ribosome biogenesis factors, searching for impact on p53. Knock-down of 4 and 35 of these proteins in U2OS cells reduced and increased p53 abundance, respectively, including p53 accumulation after depletion of BYSL, DDX56, and WDR75, the effects of which were validated in several models. Using complementary approaches including subcellular fractionation, we demonstrate that endogenous human WDR75 is a nucleolar protein and immunofluorescence analysis of ectopic GFP-tagged WDR75 shows relocation to nucleolar caps under chemically induced nucleolar stress, along with several canonical nucleolar proteins. Mechanistically, we show that WDR75 is required for pre-rRNA transcription, through supporting the maintenance of physiological levels of RPA194, a key subunit of the RNA polymerase I. Furthermore, WDR75 depletion activated the RPL5/RPL11-dependent p53 stabilization checkpoint, ultimately leading to impaired proliferation and cellular senescence. These findings reveal a crucial positive role of WDR75 in ribosome biogenesis and provide a resource of human ribosomal factors the malfunction of which affects p53.
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