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Hypomethylating drugs efficiently decrease cytosine methylation in telomeric DNA and activate telomerase without affecting telomere lengths in tobacco cells
E. Majerová, M. Fojtová, I. Mozgová, M. Bittová, J. Fajkus,
Language English Country Netherlands
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
ProQuest Central
from 1997-01-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2010-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 1997-01-01 to 1 year ago
- MeSH
- Adenine analogs & derivatives pharmacology MeSH
- Enzyme Activation drug effects MeSH
- Cytidine analogs & derivatives pharmacology MeSH
- DNA, Plant chemistry drug effects MeSH
- Epigenesis, Genetic MeSH
- Transcription, Genetic drug effects MeSH
- Cells, Cultured MeSH
- DNA Methylation drug effects MeSH
- Nucleosomes drug effects physiology MeSH
- Plant Proteins genetics metabolism MeSH
- Nicotiana cytology drug effects genetics metabolism MeSH
- Telomerase metabolism MeSH
- Telomere chemistry drug effects metabolism MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Telomere homeostasis is regulated at multiple levels, including the local chromatin structure of telomeres and subtelomeres. Recent reports demonstrated that a decrease in repressive chromatin marks, such as levels of cytosine methylation in subtelomeric regions, results in telomere elongation in mouse cells. Here we show that a considerable fraction of cytosines is methylated not only in subtelomeric, but also in telomeric DNA of tobacco BY-2 cells. Drug-induced hypomethylation (demonstrated at subtelomeric, telomeric, and global DNA levels) results in activation of telomerase. However, in contrast to mouse cells, the decrease in 5-methylcytosine levels and upregulation of telomerase do not result in any changes of telomere lengths. These results demonstrate the involvement of epigenetic mechanisms in the multilevel process of regulation of telomerase activity in plant cells and, at the same time, they indicate that changes in telomerase activity can be overridden by other factors governing telomere length stability.
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