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Dynamic PML protein nucleolar associations with persistent DNA damage lesions in response to nucleolar stress and senescence-inducing stimuli
T. Imrichova, S. Hubackova, A. Kucerova, J. Kosla, J. Bartek, Z. Hodny, P. Vasicova,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2009
Freely Accessible Science Journals
from 2009-01-01
PubMed Central
from 2009
Europe PubMed Central
from 2009
Open Access Digital Library
from 2009-01-01
PubMed
31493766
DOI
10.18632/aging.102248
Knihovny.cz E-resources
- MeSH
- Cell Nucleolus metabolism MeSH
- Doxorubicin MeSH
- Stress, Physiological MeSH
- Cells, Cultured MeSH
- Humans MeSH
- DNA Damage * MeSH
- Promyelocytic Leukemia Protein metabolism MeSH
- Cellular Senescence * MeSH
- Imaging, Three-Dimensional MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Diverse stress insults trigger interactions of PML with nucleolus, however, the function of these PML nucleolar associations (PNAs) remains unclear. Here we show that during induction of DNA damage-induced senescence in human non-cancerous cells, PML accumulates at the nucleolar periphery simultaneously with inactivation of RNA polymerase I (RNAP I) and nucleolar segregation. Using time-lapse and high-resolution microscopy, we followed the genesis, structural transitions and destiny of PNAs to show that: 1) the dynamic structural changes of the PML-nucleolar interaction are tightly associated with inactivation and reactivation of RNAP I-mediated transcription, respectively; 2) the PML-nucleolar compartment develops sequentially under stress and, upon stress termination, it culminates in either of two fates: disappearance or persistence; 3) all PNAs stages can associate with DNA damage markers; 4) the persistent, commonly long-lasting PML multi-protein nucleolar structures (PML-NDS) associate with markers of DNA damage, indicating a role of PNAs in persistent DNA damage response characteristic for senescent cells. Given the emerging evidence implicating PML in homologous recombination-directed DNA repair, we propose that PNAs contribute to sequestration and faithful repair of the highly unstable ribosomal DNA repeats, a fundamental process to maintain a precise balance between DNA repair mechanisms, with implications for genomic integrity and aging.
References provided by Crossref.org
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