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细胞对紫外线照射的敏感性由RNA聚合酶I转录介导。

Cellular sensitivity to UV-irradiation is mediated by RNA polymerase I transcription.

作者信息

Assfalg Robin, Alupei Marius Costel, Wagner Maximilian, Koch Sylvia, Gonzalez Omar Garcia, Schelling Adrian, Scharffetter-Kochanek Karin, Iben Sebastian

机构信息

Department of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.

出版信息

PLoS One. 2017 Jun 21;12(6):e0179843. doi: 10.1371/journal.pone.0179843. eCollection 2017.

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.

摘要

长期以来,核仁一直被认为是一个纯粹的核糖体工厂。然而,在过去二十年中,人们清楚地认识到,核仁除了参与核糖体生物合成外,还涉及许多其他功能。我们的实验表明,RNA聚合酶I(Pol I)转录活性可监测DNA的完整性,并影响对核仁应激的反应以及细胞存活率。核糖体DNA(rDNA)转录活性受到抑制的细胞在紫外线C(UVC)照射后,p53的稳定性增加且持续时间延长。此外,抑制后尤其是UVC照射后p53稳定性增加,可能是由于核糖体蛋白(RPs)废除了HDM2-p53降解途径。由高度活化的p53介导的细胞凋亡是科凯恩综合征细胞的典型特征,转录异常以及随后RP-HDM2-p53途径的激活可能是一种解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/5479586/60657e0982f3/pone.0179843.g001.jpg

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