SIRT7-mediated ATM deacetylation is essential for its deactivation and DNA damage repair
出版年份 2019 全文链接
标题
SIRT7-mediated ATM deacetylation is essential for its deactivation and DNA damage repair
作者
关键词
-
出版物
Science Advances
Volume 5, Issue 3, Pages eaav1118
出版商
American Association for the Advancement of Science (AAAS)
发表日期
2019-03-28
DOI
10.1126/sciadv.aav1118
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Destabilization of linker histone H1.2 is essential for ATM activation and DNA damage repair
- (2018) Zhiming Li et al. CELL RESEARCH
- Downregulation of SIRT7 by 5-fluorouracil induces radiosensitivity in human colorectal cancer
- (2017) Ming Tang et al. Theranostics
- SIRT7 promotes genome integrity and modulates non‐homologous end joining DNA repair
- (2016) Berta N Vazquez et al. EMBO JOURNAL
- SIRT7 is a histone desuccinylase that functionally links to chromatin compaction and genome stability
- (2016) Lei Li et al. Nature Communications
- NOTCH1 Inhibits Activation of ATM by Impairing the Formation of an ATM-FOXO3a-KAT5/Tip60 Complex
- (2016) Marek Adamowicz et al. Cell Reports
- A SIRT7-Dependent Acetylation Switch of GABPβ1 Controls Mitochondrial Function
- (2014) Dongryeol Ryu et al. Cell Metabolism
- DNA double-strand breaks promote methylation of histone H3 on lysine 9 and transient formation of repressive chromatin
- (2014) M. K. Ayrapetov et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Repression of RNA Polymerase I upon Stress Is Caused by Inhibition of RNA-Dependent Deacetylation of PAF53 by SIRT7
- (2013) Sifan Chen et al. MOLECULAR CELL
- KAT5 tyrosine phosphorylation couples chromatin sensing to ATM signalling
- (2013) Abderrahmane Kaidi et al. NATURE
- Genome engineering using the CRISPR-Cas9 system
- (2013) F Ann Ran et al. Nature Protocols
- SIRT7 links H3K18 deacetylation to maintenance of oncogenic transformation
- (2012) Matthew F. Barber et al. NATURE
- ATR Autophosphorylation as a Molecular Switch for Checkpoint Activation
- (2011) Shizhou Liu et al. MOLECULAR CELL
- Wolf–Hirschhorn syndrome candidate 1 is involved in the cellular response to DNA damage
- (2011) Ildiko Hajdu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- SIRT6 Promotes DNA Repair Under Stress by Activating PARP1
- (2011) Z. Mao et al. SCIENCE
- Repo-Man Controls a Protein Phosphatase 1-Dependent Threshold for DNA Damage Checkpoint Activation
- (2010) Aimin Peng et al. CURRENT BIOLOGY
- Autophosphorylation and ATM Activation
- (2010) Sergei V. Kozlov et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- SIRT1 Regulates UV-Induced DNA Repair through Deacetylating XPA
- (2010) Wei Fan et al. MOLECULAR CELL
- The DNA Damage Response: Making It Safe to Play with Knives
- (2010) Alberto Ciccia et al. MOLECULAR CELL
- Regulation of global genome nucleotide excision repair by SIRT1 through xeroderma pigmentosum C
- (2010) M. Ming et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Human SIRT6 Promotes DNA End Resection Through CtIP Deacetylation
- (2010) Abderrahmane Kaidi et al. SCIENCE
- The comet assay: A sensitive method for detecting DNA damage in individual cells
- (2009) Wenjuan Liao et al. METHODS
- Recent progress in the biology and physiology of sirtuins
- (2009) Toren Finkel et al. NATURE
- Histone H3 methylation links DNA damage detection to activation of the tumour suppressor Tip60
- (2009) Yingli Sun et al. NATURE CELL BIOLOGY
- Regulation of TIP60 by ATF2 Modulates ATM Activation
- (2008) Anindita Bhoumik et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The HINT1 tumor suppressor regulates both γ-H2AX and ATM in response to DNA damage
- (2008) Haiyang Li et al. JOURNAL OF CELL BIOLOGY
- Activation of ATM depends on chromatin interactions occurring before induction of DNA damage
- (2008) Yong-Chul Kim et al. NATURE CELL BIOLOGY
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