Coilin is rapidly recruited to UVA-induced DNA lesions and γ-radiation affects localized movement of Cajal bodies
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24859326
PubMed Central
PMC4133222
DOI
10.4161/nucl.29229
PII: 29229
Knihovny.cz E-resources
- Keywords
- Cajal bodies, DNA repair, chromatin, coilin, nucleolus, nucleus,
- MeSH
- Cell Nucleus genetics metabolism radiation effects MeSH
- Cell Line MeSH
- K562 Cells MeSH
- Coiled Bodies genetics metabolism radiation effects MeSH
- DNA genetics radiation effects MeSH
- G2 Phase genetics MeSH
- HeLa Cells MeSH
- Nuclear Proteins genetics metabolism MeSH
- Humans MeSH
- Mice MeSH
- Cell Line, Tumor MeSH
- Recombinant Fusion Proteins genetics metabolism MeSH
- Ultraviolet Rays adverse effects MeSH
- Gamma Rays adverse effects MeSH
- Green Fluorescent Proteins genetics metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA MeSH
- Nuclear Proteins MeSH
- p80-coilin MeSH Browser
- Recombinant Fusion Proteins MeSH
- Green Fluorescent Proteins MeSH
Cajal bodies are important nuclear structures containing proteins that preferentially regulate RNA-related metabolism. We investigated the cell-type specific nuclear distribution of Cajal bodies and the level of coilin, a protein of Cajal bodies, in non-irradiated and irradiated human tumor cell lines and embryonic stem (ES) cells. Cajal bodies were localized in different nuclear compartments, including DAPI-poor regions, in the proximity of chromocenters, and adjacent to nucleoli. The number of Cajal bodies per nucleus was cell cycle-dependent, with higher numbers occurring during G2 phase. Human ES cells contained a high coilin level in the nucleoplasm, but coilin-positive Cajal bodies were also identified in nuclei of mouse and human ES cells. Coilin, but not SMN, recognized UVA-induced DNA lesions, which was cell cycle-independent. Treatment with γ-radiation reduced the localized movement of Cajal bodies in many cell types and GFP-coilin fluorescence recovery after photobleaching was very fast in nucleoplasm in comparison with GFP-coilin recovery in DNA lesions. By contrast, nucleolus-localized coilin displayed very slow fluorescence recovery after photobleaching, which indicates very slow rates of protein diffusion, especially in nucleoli of mouse ES cells.
Faculty of Informatics; Masaryk University; Brno Czech Republic
Institute of Biophysics; Academy of Sciences of the Czech Republic; Brno Czech Republic
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