YAP controls retinal stem cell DNA replication timing and genomic stability.
Pauline CabochetteGuillermo A Vega-LópezJuliette BitardKarine ParainRomain ChemounyChristel MassonCaroline BordayMarie HedderichKristine A HenningfeldMorgane LockerOdile BronchainMuriel PerronPublished in: eLife (2015)
The adult frog retina retains a reservoir of active neural stem cells that contribute to continuous eye growth throughout life. We found that Yap, a downstream effector of the Hippo pathway, is specifically expressed in these stem cells. Yap knock-down leads to an accelerated S-phase and an abnormal progression of DNA replication, a phenotype likely mediated by upregulation of c-Myc. This is associated with an increased occurrence of DNA damage and eventually p53-p21 pathway-mediated cell death. Finally, we identified PKNOX1, a transcription factor involved in the maintenance of genomic stability, as a functional and physical interactant of YAP. Altogether, we propose that YAP is required in adult retinal stem cells to regulate the temporal firing of replication origins and quality control of replicated DNA. Our data reinforce the view that specific mechanisms dedicated to S-phase control are at work in stem cells to protect them from genomic instability.
Keyphrases
- stem cells
- dna damage
- cell death
- quality control
- diabetic retinopathy
- transcription factor
- neural stem cells
- optical coherence tomography
- cell therapy
- copy number
- optic nerve
- risk assessment
- oxidative stress
- mental health
- physical activity
- poor prognosis
- dendritic cells
- single molecule
- young adults
- mesenchymal stem cells
- dna methylation
- bone marrow
- machine learning
- childhood cancer
- big data
- type iii