4.8 Article

Let-7 Coordinately Suppresses Components of the Amino Acid Sensing Pathway to Repress mTORC1 and Induce Autophagy

Journal

CELL METABOLISM
Volume 20, Issue 4, Pages 626-638

Publisher

CELL PRESS
DOI: 10.1016/j.cmet.2014.09.001

Keywords

-

Funding

  1. NIH [R01 AG03382, R01 EY014997, T32 AG000216, T32 GM008666, P30 HD002274]
  2. Portuguese Foundation for Science Technology [SFRH/BPD/87552/2012, E-Rare4/0003/2012]
  3. Fundação para a Ciência e a Tecnologia [E-Rare4/0003/2012] Funding Source: FCT

Ask authors/readers for more resources

Macroautophagy (hereafter autophagy) is the major pathway by which macromolecules and organelles are degraded. Autophagy is regulated by the mTOR signaling pathway-the focal point for integration of metabolic information, with mTORC1 playing a central role in balancing biosynthesis and catabolism. Of the various inputs to mTORC1, the amino acid sensing pathway is among the most potent. Based upon transcriptome analysis of neurons subjected to nutrient deprivation, we identified let-7 microRNA as capable of promoting neuronal autophagy. We found that let-7 activates autophagy by coordinately down-regulating the amino acid sensing pathway to prevent mTORC1 activation. Let-7 induced autophagy in the brain to eliminate protein aggregates, establishing its physiological relevance for in vivo autophagy modulation. Moreover, peripheral delivery of let-7 anti-miR repressed autophagy in muscle and white fat, suggesting that let-7 autophagy regulation extends beyond CNS. Hence, let-7 plays a central role in nutrient homeostasis and proteostasis regulation in higher organisms.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available