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Published on: January 31, 2018
Lysine Crotonylation: An Emerging Player in DNA Damage Response
Yuqin Zhao1, Shuailin Hao1, Wenchi Wu1
1Beijing Key Laboratory of DNA Damage Response, College of Life Sciences, Capital Normal University, Beijing 100048, China.
Lysine crotonylation (Kcr), a novel posttranslational modification, is crucial for the DNA damage response (DDR). This review explores how Kcr regulates gene expression and DNA repair, maintaining genome stability.
Area of Science:
- Molecular Biology
- Epigenetics
- Biochemistry
Background:
- The DNA damage response (DDR) network maintains genome stability against genotoxic stress.
- Posttranslational modifications (PTMs) are key regulators within the DDR.
- Lysine crotonylation (Kcr) is an emerging PTM linking metabolism and gene regulation.
Purpose of the Study:
- To review the regulatory mechanisms of Kcr.
- To summarize Kcr's functions in the DNA damage response.
- To highlight Kcr's role in transcriptional repression and DNA repair.
Main Methods:
- Literature review of recent studies on Kcr and DDR.
- Analysis of Kcr's involvement in double-strand break (DSB) response.
- Examination of Kcr's role in DNA replication stress.
Main Results:
- Kcr is a reversible acylation modification regulated by acylases/deacylases and crotonyl-CoA.
- Kcr influences transcriptional repression following DSBs.
- Kcr is implicated in DSB repair and replication stress response.
Conclusions:
- Kcr is a significant PTM with critical roles in DDR pathways.
- Understanding Kcr regulation and function is vital for genome stability.
- Kcr represents a novel target for therapeutic interventions in related diseases.
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