p53 induces ARTS to promote mitochondrial apoptosis.
Qian HaoJiaxiang ChenJunming LiaoYingdan HuangYu GanSarit LarischShelya X ZengHua LuXiang ZhouPublished in: Cell death & disease (2021)
Apoptosis related protein in TGF-β signaling pathway (ARTS) was originally discovered in cells undergoing apoptosis in response to TGF-β, but ARTS also acts downstream of many other apoptotic stimuli. ARTS induces apoptosis by antagonizing the anti-apoptotic proteins XIAP and Bcl-2. Here we identified the pro-apoptotic Sept4/ARTS gene as a p53-responsive target gene. Ectopic p53 and a variety of p53-inducing agents increased both mRNA and protein levels of ARTS, whereas ablation of p53 reduced ARTS expression in response to multiple stress conditions. Also, γ-irradiation induced p53-dependent ARTS expression in mice. Consistently, p53 binds to the responsive DNA element on the ARTS promoter and transcriptionally activated the promoter-driven expression of a luciferase reporter gene. Interestingly, ARTS binds to and sequesters p53 at mitochondria, enhancing the interaction of the latter with Bcl-XL. Ectopic ARTS markedly augments DNA damage stress- or Nutlin-3-triggered apoptosis, while ablation of ARTS preferentially impairs p53-induced apoptosis. Altogether, these findings demonstrate that ARTS collaborates with p53 in mitochondria-engaged apoptosis.
Keyphrases
- induced apoptosis
- cell death
- endoplasmic reticulum stress
- oxidative stress
- cell cycle arrest
- signaling pathway
- dna damage
- poor prognosis
- gene expression
- pi k akt
- type diabetes
- genome wide
- binding protein
- diabetic rats
- copy number
- transcription factor
- epithelial mesenchymal transition
- adipose tissue
- transforming growth factor
- cancer therapy
- long non coding rna
- stress induced
- small molecule
- radiofrequency ablation