
| 10.1093/nar/gkaa828
http://scihub22266oqcxt.onion/10.1093/nar/gkaa828
 33068409!7708061!33068409
free
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Nucleic+Acids+Res 2020 ; 48 (21): 11890-11912 Nephropedia Template TP
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PML nuclear bodies and chromatin dynamics: catch me if you can! #MMPMID33068409Corpet A; Kleijwegt C; Roubille S; Juillard F; Jacquet K; Texier P; Lomonte PNucleic Acids Res 2020[Dec]; 48 (21): 11890-11912 PMID33068409show ga
Eukaryotic cells compartmentalize their internal milieu in order to achieve specific reactions in time and space. This organization in distinct compartments is essential to allow subcellular processing of regulatory signals and generate specific cellular responses. In the nucleus, genetic information is packaged in the form of chromatin, an organized and repeated nucleoprotein structure that is a source of epigenetic information. In addition, cells organize the distribution of macromolecules via various membrane-less nuclear organelles, which have gathered considerable attention in the last few years. The macromolecular multiprotein complexes known as Promyelocytic Leukemia Nuclear Bodies (PML NBs) are an archetype for nuclear membrane-less organelles. Chromatin interactions with nuclear bodies are important to regulate genome function. In this review, we will focus on the dynamic interplay between PML NBs and chromatin. We report how the structure and formation of PML NBs, which may involve phase separation mechanisms, might impact their functions in the regulation of chromatin dynamics. In particular, we will discuss how PML NBs participate in the chromatinization of viral genomes, as well as in the control of specific cellular chromatin assembly pathways which govern physiological mechanisms such as senescence or telomere maintenance.|*Genome, Viral[MESH]|*Protein Processing, Post-Translational[MESH]|Cell Nucleus/genetics/*metabolism/ultrastructure/virology[MESH]|Cellular Senescence[MESH]|Chromatin Assembly and Disassembly[MESH]|Chromatin/chemistry/*metabolism/ultrastructure[MESH]|Genome, Human[MESH]|Histones/genetics/metabolism[MESH]|Host-Pathogen Interactions/genetics[MESH]|Humans[MESH]|Intranuclear Inclusion Bodies/chemistry/*metabolism/ultrastructure[MESH]|Promyelocytic Leukemia Protein/*genetics/metabolism[MESH]|Small Ubiquitin-Related Modifier Proteins/genetics/metabolism[MESH]|Sumoylation[MESH]|Telomere Homeostasis[MESH]
  
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