TY - JOUR
T1 - Let-7 coordinately suppresses components of the amino acid sensing pathway to repress mTORC1 and induce autophagy
AU - Dubinsky, Amy N.
AU - Dastidar, Somasish Ghosh
AU - Hsu, Cynthia L.
AU - Zahra, Rabaab
AU - Djakovic, Stevan N.
AU - Duarte, Sonia
AU - Esau, Christine C.
AU - Spencer, Brian
AU - Ashe, Travis D.
AU - Fischer, Kimberlee M.
AU - Mackenna, Deidre A.
AU - Sopher, Bryce L.
AU - Masliah, Eliezer
AU - Gaasterland, Terry
AU - Chau, B. Nelson
AU - Pereira De Almeida, Luis
AU - Morrison, Bradley E.
AU - La Spada, Albert R.
N1 - Publisher Copyright:
© 2014 Elsevier Inc.
PY - 2014/10/7
Y1 - 2014/10/7
N2 - 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 downregulating 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.
AB - 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 downregulating 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.
UR - http://www.scopus.com/inward/record.url?scp=84907967415&partnerID=8YFLogxK
U2 - 10.1016/j.cmet.2014.09.001
DO - 10.1016/j.cmet.2014.09.001
M3 - Article
C2 - 25295787
AN - SCOPUS:84907967415
SN - 1550-4131
VL - 20
SP - 626
EP - 638
JO - Cell Metabolism
JF - Cell Metabolism
IS - 4
ER -