mTOR signaling regulates central and peripheral circadian clock function
What this study shows
mTOR sets how fast and how strongly the circadian clock ticks. Inhibiting mTOR lengthened the clock period and flattened its amplitude; activating it shortened the period and raised the amplitude, in cells, in ex vivo brain (SCN) and liver clocks, and in mTOR heterozygous mice, whose locomotor rhythm ran longer. The study starts from the observation that mTOR activity itself oscillates over 24 hours in many tissues.
Abstract
ShowHide
The circadian clock coordinates physiology and metabolism. mTOR (mammalian/mechanistic target of rapamycin) is a major intracellular sensor that integrates nutrient and energy status to regulate protein synthesis, metabolism, and cell growth. Previous studies have identified a key role for mTOR in regulating photic entrainment and synchrony of the central circadian clock in the suprachiasmatic nucleus (SCN).
Read the full abstract on PubMed →At a glance
ShowHide
| Evidence type | A Animal model Marked A because it is an animal intervention or observation study measuring an organismal outcome (model: Hepatocyte and adipocyte clock models; Tsc2-/- fibroblasts; ex vivo SCN and liver; mTOR heterozygous mice); the code names the system studied -- animal work can be rigorous and still not be human data. |
| Study type | 4 - Animal Study |
| Model system | Hepatocyte and adipocyte clock models; Tsc2-/- fibroblasts; ex vivo SCN and liver; mTOR heterozygous mice |
| Journal | PLOS Genetics |
| Year | 2018 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1371/journal.pgen.1007369 · PMID 29750810 · Free full text (PMC5965903) |
Where this study fits
How this study connects to the pathway map, open questions, people and other studies in the Atlas.
People in the Atlas
-
Circadian biologist at the University of Memphis who showed that mTOR signalling sets the speed and strength of the body's daily clocks
-
Circadian biologist who studies how the body clock works at the molecular level and how it connects with metabolism and signalling pathways such as mTOR.
-
Circadian-rhythm geneticist who uses genome-wide methods to map which genes the body clock controls in each tissue.
More: 5 other authors
No profile yet: Kathale ND, Liu D, Lee C, Freeman DA, Cao R
Related studies
- A Impaired mTOR/SREBP1-Mediated Lipogenesis as a Mechanism of Hepatic Glycogen Accumulation in a Carnivorous Fish Model, Largemouth Bass (Micropterus salmoides)
TAO2026 · 2026 · Shares: TSC1/TSC2, Rapamycin, mTOR
- M The TSC-mTOR signaling pathway regulates the innate inflammatory response
WEI2008 · 2008 · Shares: TSC1/TSC2, Rapamycin, mTOR
- M Excitatory/inhibitory synaptic imbalance leads to hippocampal hyperexcitability in mouse models of tuberous sclerosis
BAT2013 · 2013 · Shares: TSC1/TSC2, Rapamycin
- H Dissecting the genetic basis of focal cortical dysplasia: a large cohort study.
BAL2019 · 2019 · Shares: TSC1/TSC2, mTOR
- A Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice
TSA2012 · 2012 · Shares: TSC1/TSC2, Rapamycin
More related studies
- A
- M ATM signals to TSC2 in the cytoplasm to regulate mTORC1 in response to ROS
ALE2010 · 2010 · Shares: TSC1/TSC2
- M mTORC1 in the Paneth cell niche couples intestinal stem-cell function to calorie intake
YIL2012 · 2012 · Shares: TSC1/TSC2, Rapamycin
- M Regulation of TFEB and V-ATPases by mTORC1
PEN2011 · 2011 · Shares: TSC1/TSC2, Rapamycin
- A mTOR regulation and therapeutic rejuvenation of aging hematopoietic stem cells
CHE2009 · 2009 · Shares: TSC1/TSC2, Rapamycin
- A Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis
EHN2008 · 2008 · Shares: TSC1/TSC2, Rapamycin
- A
- A Rapamycin prevents epilepsy in a mouse model of tuberous sclerosis complex
ZEN2008 · 2008 · Shares: TSC1/TSC2, Rapamycin
Topics
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | Genetic and pharmacological mTOR inhibition or activation |
| Target | mTOR; core clock proteins (CRY1, BMAL1, CLOCK) |
| Model | Mouse (cells, ex vivo tissue, whole animal) |
| Effect | mTOR inhibition lengthens circadian period and dampens amplitude; activation does the opposite |
Thank you. Your answer was counted anonymously.