p53-dependent chromatin relaxation is required for DNA double-strand break repair
The tumor suppressor p53, an indispensable nuclear transcription factor, plays a central role in orchestrating cellular responses when DNA damage occurs. In this study, we demonstrate that in the initial phases of DNA double-strand break (DSB) repair, p53 is rapidly recruited to sites of damage and...
Saved in:
| Main Authors: | Chen Hongyu, Shan Jin, Qi Wenjing, Chen Lili, Zeng Xianlu |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
China Science Publishing & Media Ltd.
2025-02-01
|
| Series: | Acta Biochimica et Biophysica Sinica |
| Subjects: | |
| Online Access: | https://www.sciengine.com/doi/10.3724/abbs.2025008 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The histone acetyltransferase CBP participates in regulating the DNA damage response through ATM after double-strand breaks
by: Wafaa S. Ramadan, et al.
Published: (2025-04-01) -
Cell Senescence and the DNA Single-Strand Break Damage Repair Pathway
by: Parvathy A. Sarma, et al.
Published: (2024-12-01) -
Suboptimal extracellular pH values alter DNA damage response to induced double‐strand breaks
by: Julien Massonneau, et al.
Published: (2018-03-01) -
Piceatannol reduces radiation-induced DNA double-strand breaks by suppressing superoxide production and enhancing ATM-dependent repair efficiency
by: Tomoya Suzuki, et al.
Published: (2024-12-01) -
Exposure of cells to near-infrared irradiation relaxes chromatin compaction and facilitates recognition of cyclo-butane pyrimidine dimers
by: Beata Plitta-Michalak, et al.
Published: (2025-07-01)