Your browser doesn't support javascript.
loading
Cellular sensitivity to UV-irradiation is mediated by RNA polymerase I transcription.
Assfalg, Robin; Alupei, Marius Costel; Wagner, Maximilian; Koch, Sylvia; Gonzalez, Omar Garcia; Schelling, Adrian; Scharffetter-Kochanek, Karin; Iben, Sebastian.
Afiliação
  • Assfalg R; Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
  • Alupei MC; Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
  • Wagner M; Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
  • Koch S; Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
  • Gonzalez OG; Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
  • Schelling A; Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
  • Scharffetter-Kochanek K; Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
  • Iben S; Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
PLoS One ; 12(6): e0179843, 2017.
Article em En | MEDLINE | ID: mdl-28636660
ABSTRACT
The nucleolus has long been considered to be a pure ribosome factory. However, over the last two decades it became clear that the nucleolus is involved in numerous other functions besides ribosome biogenesis. Our experiments indicate that the activity of RNA polymerase I (Pol I) transcription monitors the integrity of the DNA and influences the response to nucleolar stress as well as the rate of survival. Cells with a repressed ribosomal DNA (rDNA) transcription activity showed an increased and prolonged p53 stabilisation after UVC-irradiation. Furthermore, p53 stabilisation after inhibition and especially after UVC-irradiation might be due to abrogation of the HDM2-p53 degradation pathway by ribosomal proteins (RPs). Apoptosis mediated by highly activated p53 is a typical hallmark of Cockayne syndrome cells and transcriptional abnormalities and the following activation of the RP-HDM2-p53 pathway would be a possible explanation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article