4.8 Article

The tight junction protein TJP1 regulates the feeding-modulated hepatic circadian clock

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NATURE COMMUNICATIONS
卷 11, 期 1, 页码 -

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NATURE RESEARCH
DOI: 10.1038/s41467-020-14470-2

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  1. Ministry of Science and Technology of the People's Republic of China [2017YFA0503404, 2016YFC1304803]
  2. National Natural Science Foundation of China [31625014, 31621063, 31830040, 91957206]

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Circadian clocks in the suprachiasmatic nucleus and peripheral tissues orchestrate behavioral and physiological activities of mammals in response to environmental cues. In the liver, the circadian clock is also modulated by feeding. However, the molecular mechanisms involved are unclear. Here, we show that TJP1 (tight junction protein 1) functions as a mediator of mTOR (mechanistic target of rapamycin) to modulate the hepatic circadian clock. TJP1 interacts with PER1 (period circadian regulator 1) and prevents its nuclear translocation. During feeding, mTOR phosphorylates TJP1 and attenuates its association with PER1, thereby enhancing nuclear shuttling of PER1 to dampen circadian oscillation. Therefore, our results provide a previously uncharacterized mechanistic insight into how feeding modulates the hepatic circadian clock. The circadian clock regulates rhythms of physiology and metabolism in response to environmental cues such as food intake. Here, the authors show that tight junction protein 1 (TJP1) interacts with period 1 and modulates its nuclear translocation in a mTOR-dependent manner.

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