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Irradiation by gamma-rays reduces the level of H3S10 phosphorylation and weakens the G2 phase-dependent interaction between H3S10 phosphorylation and gamma H2AX

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F18%3A00101337" target="_blank" >RIV/00216224:14740/18:00101337 - isvavai.cz</a>

  • Alternative codes found

    RIV/68081707:_____/18:00501694

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.biochi.2018.07.029" target="_blank" >http://dx.doi.org/10.1016/j.biochi.2018.07.029</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.biochi.2018.07.029" target="_blank" >10.1016/j.biochi.2018.07.029</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Irradiation by gamma-rays reduces the level of H3S10 phosphorylation and weakens the G2 phase-dependent interaction between H3S10 phosphorylation and gamma H2AX

  • Original language description

    Histone posttranslational modifications regulate diverse nuclear functions, including DNA repair. Here, we use mass spectrometry, western blotting, immunohistochemistry and advanced confocal microscopy in order to show radiation-specific changes in the histone signature. We studied wild-type mouse embryonic stem cells (mESCs) and mESCs with a depletion of histone deacetylase 1 (HDAC1), which plays a role in DNA repair. Irradiation by gamma-rays increased the S139 phosphorylation of histone H2AX but reduced the level of the H3K9-R17 peptide, which contains S10 phosphorylation (H3S10ph). On an individual cellular level, H3S10ph was low in highly gamma H2AX-positive UV laser-induced DNA lesions, and this nuclear distribution pattern was not changed by HDAC1 depletion. Despite this fact, spontaneous gamma H2AX-positive DNA lesions colocalized with large H3S10ph-positive nuclear bodies that appear in the G2 phase of the cell cycle. Similarly, by FLIM-FRET analysis, we observed an interaction between H3S10ph and gamma H2AX in the G2 phase. However, this interaction was reduced when cells were exposed to gamma-rays. A mutual link between H3S10ph and gamma H2AX was not observed in the G1 phase of the cell cycle. Together, our data show that despite the fact that H3S10ph is not directly involved in DNA repair, a decrease in H3S10 phosphorylation and weakened interaction between H3S10ph and gamma H2AX is a result of radiation-induced damage of the genome. In this case, gamma-irradiation also decreased the number of cells in the G1 phase, characterized by no interaction between H3S10ph and gamma H2AX. (C) 2018 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM).

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Biochimie

  • ISSN

    0300-9084

  • e-ISSN

    1638-6183

  • Volume of the periodical

    154

  • Issue of the periodical within the volume

    NOV

  • Country of publishing house

    FR - FRANCE

  • Number of pages

    13

  • Pages from-to

    86-98

  • UT code for WoS article

    000448032300011

  • EID of the result in the Scopus database

    2-s2.0-85051397331