Time-series transcriptomics and proteomics reveal alternative modes to decode p53 oscillations

ABSTRACT: The cell stress responsive transcription factor p53 influences the expression of its target genes and subsequent cellular responses, based in part on its dynamics (changes in level over time). The mechanisms decoding p53 dynamics into subsequent target mRNA and protein dynamics remain unclear. We systematically quantified p53 target mRNA and protein expression over time under two p53 dynamical regimes, oscillatory and sustained, using RNA-sequencing and TMT mass-spectrometry. Oscillatory dynamics allowed for a greater variety of dynamical patterns for both mRNAs and proteins. Mathematical modeling of empirical data revealed three distinct mechanisms that decode p53 dynamics. Specific combinations of these mechanisms at the transcriptional and post-transcriptional levels enabled exclusive

SUBMITTER: Dr Alba Jiménez 

PROVIDER: S-SCDT-MSB-2021-10588 | biostudies-other |

REPOSITORIES: biostudies-other