FALK, Martin, Emilie LUKÁŠOVÁ, Lenka ŠTEFANČÍKOVÁ, E BARANOVÁ, I FALKOVÁ, L JEŽKOVÁ, M Bačíková A DAVÍDKOVÁ, J VACHELOVÁ, A MICHAELIDESOVÁ and Stanislav KOZUBEK. Heterochromatinization associated with cell differentiation as a model to study DNA double strandbreak induction and repair in the context of higher-order chromatin structure. Applied Radiation and Isotopes. Elsevier, 2014, vol. 83, p. 177-185. ISSN 0969-8043. Available from: https://dx.doi.org/10.1016/j.apradiso.2013.01.029.
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Basic information
Original name Heterochromatinization associated with cell differentiation as a model to study DNA double strandbreak induction and repair in the context of higher-order chromatin structure
Authors FALK, Martin, Emilie LUKÁŠOVÁ, Lenka ŠTEFANČÍKOVÁ, E BARANOVÁ, I FALKOVÁ, L JEŽKOVÁ, M Bačíková A DAVÍDKOVÁ, J VACHELOVÁ, A MICHAELIDESOVÁ and Stanislav KOZUBEK.
Edition Applied Radiation and Isotopes, Elsevier, 2014, 0969-8043.
Other information
Original language English
Type of outcome Article in a journal
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 1.231
Doi http://dx.doi.org/10.1016/j.apradiso.2013.01.029
Tags International impact, Reviewed
Changed by Changed by: doc. RNDr. Martin Falk, Ph.D., učo 9835. Changed: 19/12/2019 13:50.
Abstract
Cell differentiation is associated with extensive gene silencing, heterochromatinization and potentially decreasing need for repairing DNA double-strand breaks (DSBs). Differentiation stages of blood cells thus represent an excellent model to study DSB induction, repair and misrepair in the context of changing higher-order chromatin structure. We show that immature granulocytes form γH2AX and 53BP1 foci, contrary to the mature cells; however, these foci colocalize only rarely and DSB repair is inefficient. Moreover, specific chromatin structure of granulocytes probably influences DSB induction.
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