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PA200-Mediated Proteasomal Protein Degradation and Regulation of Cellular Senescence.

Pei WenYan SunTian-Xia JiangXiao-Bo Qiu
Published in: International journal of molecular sciences (2024)
Cellular senescence is closely related to DNA damage, proteasome inactivity, histone loss, epigenetic alterations, and tumorigenesis. The mammalian proteasome activator PA200 (also referred to as PSME4) or its yeast ortholog Blm10 promotes the acetylation-dependent degradation of the core histones during transcription, DNA repair, and spermatogenesis. According to recent studies, PA200 plays an important role in senescence, probably because of its role in promoting the degradation of the core histones. Loss of PA200 or Blm10 is a major cause of the decrease in proteasome activity during senescence. In this paper, recent research progress on the association of PA200 with cellular senescence is summarized, and the potential of PA200 to serve as a therapeutic target in age-related diseases is discussed.
Keyphrases
  • dna damage
  • dna repair
  • oxidative stress
  • endothelial cells
  • stress induced
  • dna damage response
  • gene expression
  • immune response
  • amino acid
  • binding protein