ログイン
言語:

WEKO3

  • トップ
  • ランキング
To
lat lon distance
To

Field does not validate



インデックスリンク

インデックスツリー

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. 学会発表・講演等
  2. ポスター発表

Most hydrogen peroxide-induced histone H2AX phosphorylation is mediated by ATR and is not dependent on DNA double-strand breaks

https://repo.qst.go.jp/records/71472
https://repo.qst.go.jp/records/71472
2d549b57-d32a-41a8-9843-0a1a1c56a646
Item type 会議発表用資料 / Presentation(1)
公開日 2014-06-17
タイトル
タイトル Most hydrogen peroxide-induced histone H2AX phosphorylation is mediated by ATR and is not dependent on DNA double-strand breaks
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 勝部, 孝則

× 勝部, 孝則

WEKO 702752

勝部, 孝則

Search repository
森, 雅彦

× 森, 雅彦

WEKO 702753

森, 雅彦

Search repository
辻, 秀雄

× 辻, 秀雄

WEKO 702754

辻, 秀雄

Search repository
塩見, 忠博

× 塩見, 忠博

WEKO 702755

塩見, 忠博

Search repository
王, 冰

× 王, 冰

WEKO 702756

王, 冰

Search repository
Qiang, Liu

× Qiang, Liu

WEKO 702757

Qiang, Liu

Search repository
根井, 充

× 根井, 充

WEKO 702758

根井, 充

Search repository
小野田, 眞

× 小野田, 眞

WEKO 702759

小野田, 眞

Search repository
勝部 孝則

× 勝部 孝則

WEKO 702760

en 勝部 孝則

Search repository
森 雅彦

× 森 雅彦

WEKO 702761

en 森 雅彦

Search repository
辻 秀雄

× 辻 秀雄

WEKO 702762

en 辻 秀雄

Search repository
塩見 忠博

× 塩見 忠博

WEKO 702763

en 塩見 忠博

Search repository
王 冰

× 王 冰

WEKO 702764

en 王 冰

Search repository
根井 充

× 根井 充

WEKO 702765

en 根井 充

Search repository
小野田 眞

× 小野田 眞

WEKO 702766

en 小野田 眞

Search repository
抄録
内容記述タイプ Abstract
内容記述 The nuclear foci of phosphorylated histone H2AX (γH2AX) are frequently used as a marker for DNA double-strand breaks (DSBs) following ionizing radiation (IR). However, recent studies reported that γH2AX foci do not necessarily correlate with DSBs under other conditions. We showed that γH2AX foci induced by oxidative stress in hydrogen peroxide (H2O2)-treated cells displayed several different features from those induced by IR. The magnitude of γH2AX induction was heterogeneous among H2O2-treated cells.
Some cells expressed small discrete γH2AX foci, whereas others expressed a gross γH2AX signal that was distributed throughout the nucleus. Oxidative stress-induced γH2AX was eliminated in DSB repair-deficient mutant cells as efficiently as in wild-type cells and was not necessarily accompanied by phosphorylated ATM or
53BP1 foci. Analyses using specific inhibitors showed that ATR, rather than ATM, was the prominent kinase mediating the oxidative stress response. These results suggest that a major fraction of γH2AX induced by oxidative stress is not associated with DSBs.
Single-stranded DNA arisen from stalled replication forks can cause the ATR-mediated induction of γH2AX. However, oxidative stress appeared to induce γH2AX in both S- and non-S-phase cells.
These results suggest that there may be another pathway leading to the ATR-mediated induction of γH2AX in non-S-phase cells without DSBs.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 The 2nd Global Chinese Congress of Radiation Research(GCCRR2014)
発表年月日
日付 2014-05-12
日付タイプ Issued
戻る
0
views
See details
Views

Versions

Ver.1 2023-05-15 19:50:51.874686
Show All versions

Share

Mendeley Twitter Facebook Print Addthis

Cite as

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX

Confirm


Powered by WEKO3


Powered by WEKO3