Detailed Information on Publication Record
2015
Cell cycle-dependent changes in H3K56ac in human cells.
STEJSKAL, Stanislav, Karel ŠTĚPKA, Lenka TESAŘOVÁ, Karel STEJSKAL, Martina MATĚJKOVÁ et. al.Basic information
Original name
Cell cycle-dependent changes in H3K56ac in human cells.
Authors
STEJSKAL, Stanislav (203 Czech Republic, belonging to the institution), Karel ŠTĚPKA (203 Czech Republic, belonging to the institution), Lenka TESAŘOVÁ (203 Czech Republic, belonging to the institution), Karel STEJSKAL (203 Czech Republic, belonging to the institution), Martina MATĚJKOVÁ (203 Czech Republic, belonging to the institution), Pavel ŠIMARA (203 Czech Republic, belonging to the institution), Zbyněk ZDRÁHAL (203 Czech Republic, belonging to the institution) and Irena KRONTORÁD KOUTNÁ (203 Czech Republic, guarantor, belonging to the institution)
Edition
Cell Cycle, Philadelphia, Taylor&Francis Inc, 2015, 1538-4101
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.952
RIV identification code
RIV/00216224:14330/15:00081398
Organization unit
Faculty of Informatics
UT WoS
000367063200017
Keywords in English
Cell cycle; Chromatin; DNA replication; H3K56ac; Mammalian cells; Nucleosome
Tags
International impact, Reviewed
Změněno: 16/12/2019 16:41, Mgr. Marie Šípková, DiS.
Abstract
V originále
The incorporation of histone H3 with an acetylated lysine 56 (H3K56ac) into the nucleosome is important for chromatin remodeling and serves as a marker of new nucleosomes during DNA replication and repair in yeast. However, in human cells, the level of H3K56ac is greatly reduced, and its role during the cell cycle is controversial. Our aim was to determine the potential of H3K56ac to regulate cell cycle progression in different human cell lines. A significant increase in the number of H3K56ac foci, but not in H3K56ac protein levels, was observed during the S and G2 phases in cancer cell lines, but was not observed in embryonic stem cell lines. Despite this increase, the H3K56ac signal was not present in late replication chromatin, and H3K56ac protein levels did not decrease after the inhibition of DNA replication. H3K56ac was not tightly associated with the chromatin and was primarily localized to active chromatin regions. Our results support the role of H3K56ac in transcriptionally active chromatin areas but do not confirm H3K56ac as a marker of newly synthetized nucleosomes in DNA replication.
Links
CZ.1.07/2.3.00/30.0030, interní kód MU |
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ED1.1.00/02.0068, research and development project |
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GBP206/12/G151, research and development project |
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GBP302/12/G157, research and development project |
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