Weak coupling between intracellular feedback loops explains dissociation of clock gene dynamics.
Christoph SchmalDaisuke OnoJihwan MyungJan Patrick PettSato HonmaKen-Ichi HonmaHanspeter HerzelIsao T TokudaPublished in: PLoS computational biology (2019)
Circadian rhythms are generated by interlocked transcriptional-translational negative feedback loops (TTFLs), the molecular process implemented within a cell. The contributions, weighting and balancing between the multiple feedback loops remain debated. Dissociated, free-running dynamics in the expression of distinct clock genes has been described in recent experimental studies that applied various perturbations such as slice preparations, light pulses, jet-lag, and culture medium exchange. In this paper, we provide evidence that this "presumably transient" dissociation of circadian gene expression oscillations may occur at the single-cell level. Conceptual and detailed mechanistic mathematical modeling suggests that such dissociation is due to a weak interaction between multiple feedback loops present within a single cell. The dissociable loops provide insights into underlying mechanisms and general design principles of the molecular circadian clock.
Keyphrases
- single cell
- gene expression
- rna seq
- electron transfer
- genome wide
- high throughput
- dna methylation
- poor prognosis
- transcription factor
- genome wide identification
- stem cells
- working memory
- magnetic resonance
- cell therapy
- computed tomography
- copy number
- high frequency
- brain injury
- reactive oxygen species
- mesenchymal stem cells
- case control
- bone marrow
- heat stress