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Transcriptional Basis for Rhythmic Control of Hunger and Metabolism within the AgRP Neuron.

Citation
Cedernaes, J., et al. “Transcriptional Basis For Rhythmic Control Of Hunger And Metabolism Within The Agrp Neuron.”. Cell Metabolism, pp. 1078-1091.e5.
Center University of Chicago
Author Jonathan Cedernaes, Wenyu Huang, Kathryn Moynihan Ramsey, Nathan Waldeck, Lei Cheng, Biliana Marcheva, Chiaki Omura, Yumiko Kobayashi, Clara Bien Peek, Daniel C Levine, Ravindra Dhir, Raj Awatramani, Christopher A Bradfield, Xiaozhong A Wang, Joseph S Takahashi, Mohamad Mokadem, Rexford S Ahima, Joseph Bass
Keywords AgRP, Agouti-related protein, RNA sequencing, RNA-seq, RiboTag, SCN, circadian, Metabolism, Suprachiasmatic nucleus, time-restricted feeding
Abstract

The alignment of fasting and feeding with the sleep/wake cycle is coordinated by hypothalamic neurons, though the underlying molecular programs remain incompletely understood. Here, we demonstrate that the clock transcription pathway maximizes eating during wakefulness and glucose production during sleep through autonomous circadian regulation of NPY/AgRP neurons. Tandem profiling of whole-cell and ribosome-bound mRNAs in morning and evening under dynamic fasting and fed conditions identified temporal control of activity-dependent gene repertoires in AgRP neurons central to synaptogenesis, bioenergetics, and neurotransmitter and peptidergic signaling. Synaptic and circadian pathways were specific to whole-cell RNA analyses, while bioenergetic pathways were selectively enriched in the ribosome-bound transcriptome. Finally, we demonstrate that the AgRP clock mediates the transcriptional response to leptin. Our results reveal that time-of-day restriction in transcriptional control of energy-sensing neurons underlies the alignment of hunger and food acquisition with the sleep/wake state.

Year of Publication
2019
Journal
Cell metabolism
Volume
29
Issue
5
Number of Pages
1078-1091.e5
Date Published
12/2019
ISSN Number
1932-7420
DOI
10.1016/j.cmet.2019.01.023
Alternate Journal
Cell Metab.
PMID
30827863
PMCID
PMC6506361
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