| Literature DB >> 31365120 |
Isabel Saez1, Jennifer V Gerbracht2, Seda Koyuncu1, Hyun Ju Lee1, Moritz Horn3, Virginia Kroef3, Martin S Denzel3, Christoph Dieterich4, Niels H Gehring2, David Vilchez1.
Abstract
UBR5 is an E3 ubiquitin ligase involved in distinct processes such as transcriptional regulation and development. UBR5 is highly upregulated in embryonic stem cells (ESCs), whereas its expression decreases with differentiation, suggesting a role for UBR5 in ESC function. However, little is known about how UBR5 regulates ESC identity. Here, we define the protein interactome of UBR5 in ESCs and find interactions with distinct components of the H/ACA ribonucleoprotein complex, which is required for proper maturation of ribosomal RNA (rRNA). Notably, loss of UBR5 induces an abnormal accumulation of rRNA processing intermediates, resulting in diminished ribosomal levels. Consequently, lack of UBR5 triggers an increase in p53 levels and a concomitant decrease in cellular proliferation rates. Thus, our results indicate a link between UBR5 and rRNA maturation.Entities:
Keywords: embryonic stem cells; protein-protein interactions; ribosomal RNA; ribosome; ubiquitin ligases
Year: 2019 PMID: 31365120 DOI: 10.1002/1873-3468.13559
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124