Dynamic transcriptome profiling in DNA damage-induced cellular senescence and transient cell-cycle arrest
Open accessAbstract
Cellular senescence is an irreversible cell cycle arrest process associated with aging and senescence-related diseases. DNA damage is an extensive feature of cellular senescence and aging. Different levels of DNA damage could lead to cellular senescence or transient cell-cycle arrest, but the genetic regulatory mechanisms determining cell fate are still not clear. In this work, high-resolution time course analysis of gene expression in DNA damage-induced cellular senescence and transient cell-cycle arrest was used to explore the transcriptomic differences between different cell fates after DNA damage response and to investigate the key regulatory factors affecting senescent cell fates. Pathways such as the cell cycle, DNA repair and cholesterol metabolism showed characteristic differential response. A number of key transcription factors were predicted to regulating cell cycle and DNA repair. Our study provides genome-wide insights into the molecular-level mechanisms of senescent cell fate decisions after DNA damage response.
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SID scores hardly change at 2 h after low- or high-dose bleomycin treatments.
“We show in a time-series dataset that SID scores hardly change at 2 h right after low- or high-dose of bleomycin treatments, when almost all cells had DNA damage foci in both groups.45”
From Single-cell senescence identification reveals senescence heterogeneity, trajectory, and modulators (2024) · cites this paper as [45]
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- Authors
- Zhao, Z., Dong, Q., Liu, X., Wei, L., Liu, L., Li, Y., & Wang, X.
- Affiliations
- Beijing National Research Center for Information Science and Technology (CN)
- Corresponding author
- Wang, Xiaowo
- Venue
- Genomics
- Publisher
- Elsevier BV
- Published
- 2020-03
- Volume
- 112
- Issue
- 2
- Pages
- 1309-1317
- ISSN
- 0888-7543 (ISSN-L)
- OpenAlex
- W2965516837
- Cited by
- 37
- References
- 66
- Citations by year
- 2026: 1 · 2025: 6 · 2024: 8 · 2023: 8 · 2022: 6 · 2021: 7 · 2020: 1
- FWCI
- 2.41
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Genomics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Natural Science Foundation of China
- Topics
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- cellular senescence, DNA damage response, temporal gene expression, cell fate determination, DNA repair, cholesterol metabolism, cell cycle, transcription factors, aging
- MeSH terms
- Cell Line, Cholesterol, DNA Damage, Humans, Transcription Factors, Cellular Senescence, Cell Cycle Checkpoints, Transcriptome
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