Jun dimerization protein 2 in oxygen restriction; control of senescence
Shin-Wei Wang1, Jiag-Ki Lee, Chia-Chen Ku
1Cancer Center, Kaohsiung Medical University, Taiwan.
Abstract:
Senescent cells show a series of alterations, including a flat and enlarged morphology, increase in nonspecific acidic β- galactosidase activity, chromatin condensation, and changes in gene expression patterns. The onset and maintenance of senescence are regulated by two tumor suppressor proteins, p53 and Rb, whose expression is controlled by two distinct proteins, p19(Arf) and p16(Ink4a), respectively, which are encoded by the cdkn2a locus. Transcription factor Jun dimerization protein 2 (JDP2) which binds directly to histones and DNA, inhibits the acetylation and methylation of core histones and of reconstituted nucleosomes that contain JDP2-recognition DNA sequences. JDP2-deficient mouse embryonic fibroblasts are known to be resistant to replicative senescence. Oxygen induces the expression of the JDP2 gene and JDP2 then inhibits the recruitment of polycomb repressive complexes (PRCs1 and 2) to the promoter of the gene encoding p16(Ink4a), resulting in the inhibition of methylation of lysine 27 of histone H3. These findings suggest that chromatin-remodeling factors, including the PRC complex controlled by JDP2, are important players in the senescence. The newly defined mechanisms that underlie the action of oxygen in the induction of JDP2 and cellular senescence are reviewed.
Insights
Oxygen induces Jun dimerization protein 2 (JDP2), a factor that inhibits polycomb repressive complexes and p16Ink4a methylation, thereby promoting cellular senescence. This highlights JDP2
Area of Science:
- Cellular senescence
- Molecular biology
- Epigenetics
Background:
- Cellular senescence involves morphological and molecular changes, regulated by tumor suppressors p53 and Rb.
- p53 and Rb expression are controlled by p19Arf and p16Ink4a, encoded by the cdkn2a locus.
Purpose of the Study:
- To investigate the role of Jun dimerization protein 2 (JDP2) in oxygen-induced cellular senescence.
- To elucidate the molecular mechanisms by which JDP2 influences senescence pathways.
Main Methods:
- Studied JDP2's interaction with histones and DNA.
- Analyzed JDP2's effect on histone acetylation and methylation.
- Investigated JDP2's role in regulating polycomb repressive complexes (PRCs) and p16Ink4a expression.
- Examined JDP2-deficient mouse embryonic fibroblasts' resistance to senescence.
Main Results:
- JDP2 binds to histones and DNA, inhibiting core histone acetylation and methylation.
- Oxygen induces JDP2 expression.
- JDP2 inhibits PRC recruitment to the p16Ink4a promoter, preventing H3K27 methylation.
- JDP2-deficient cells are resistant to replicative senescence.
Conclusions:
- JDP2 is a key mediator of oxygen-induced cellular senescence.
- Chromatin remodeling factors, including JDP2-controlled PRCs, are crucial for senescence.
- The study defines novel mechanisms of oxygen's action on JDP2 and senescence.
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