Cargando…

An inducible long noncoding RNA amplifies DNA damage signaling

Long noncoding RNAs (lncRNAs) are prevalent genes with frequently exquisite regulation but mostly unknown functions. Here we demonstrate a role of lncRNAs in guiding organismal DNA damage response. DNA damage activates transcription of DINO (Damage Induced NOncoding) via p53. DINO is required for p5...

Descripción completa

Detalles Bibliográficos
Autores principales: Schmitt, Adam M., Garcia, Julia T., Hung, Tiffany, Flynn, Ryan A., Shen, Ying, Qu, Kun, Payumo, Alexander Y., Peres-da-Silva, Ashwin, Broz, Daniela Kenzelmann, Baum, Rachel, Guo, Shuling, Chen, James K., Attardi, Laura D., Chang, Howard Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5083181/
https://www.ncbi.nlm.nih.gov/pubmed/27668660
http://dx.doi.org/10.1038/ng.3673
Descripción
Sumario:Long noncoding RNAs (lncRNAs) are prevalent genes with frequently exquisite regulation but mostly unknown functions. Here we demonstrate a role of lncRNAs in guiding organismal DNA damage response. DNA damage activates transcription of DINO (Damage Induced NOncoding) via p53. DINO is required for p53-dependent gene expression, cell cycle arrest, and apoptosis in response to DNA damage, and DINO expression suffice to activate damage signaling and cell cycle arrest in the absence of DNA damage. DINO binds to and promotes p53 protein stabilization, mediating a p53 auto-amplification loop. Dino knockout or promoter inactivation in mice dampens p53 signaling and ameliorates acute radiation syndrome in vivo. Thus, inducible lncRNA can create a feedback loop with its cognate transcription factor to amplify cellular signaling networks.