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Coilin is rapidly recruited to UVA-induced DNA lesions and γ-radiation affects localized movement of Cajal bodies
E. Bártová, V. Foltánková, S. Legartová, P. Sehnalová, DV. Sorokin, J. Suchánková, S. Kozubek,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2010 to 1 year ago
PubMed Central
from 2010
Europe PubMed Central
from 2010 to 1 year ago
Taylor & Francis Open Access
from 2010-01-01
Medline Complete (EBSCOhost)
from 2011-11-01
PubMed
24859326
DOI
10.4161/nucl.29229
Knihovny.cz E-resources
- 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
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.
References provided by Crossref.org
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