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Epigenetic reshaping through damage: promoting cell fate transition by BrdU and IdU incorporation.

Chuang LiXiaoduo XuShuyan ChenAnchun XuTongxing GuanHaokaifeng WuDuanqing PeiJing Liu
Published in: Cell & bioscience (2024)
Overall, our study finds that BrdU/IdU can activate the DNA damage repair pathway (HRR), leading to increased histone acetylation and genome-wide DNA demethylation, regulating somatic cell reprogramming. This offers valuable insights into mechanisms underlying cell fate transition.
Keyphrases
  • cell fate
  • dna methylation
  • dna damage
  • genome wide
  • oxidative stress
  • copy number
  • gene expression
  • single cell
  • circulating tumor
  • dna repair
  • cell therapy
  • stem cells
  • circulating tumor cells