TY - JOUR
T1 - Circadian control of oscillations in mitochondrial rate-limiting enzymes and nutrient utilization by PERIOD proteins
AU - Neufeld - Cohen, Adi
AU - Robles, MS
AU - Aviram, Rona
AU - Manella, Gal
AU - Adamovich, Yaarit
AU - Ladeuix, Benjamin
AU - Nir, Dana
AU - Rousso Noori, Noori, Liat
AU - Kuperman, Yael
AU - Golik, Marina
AU - Mann, Mati
AU - Asher, Gad
AU - Mann, Matthias
N1 - Feinberg Graduate School, Weizmann Institute of Science; Israel Science Foundation Grant [ISF 138/12]; Abish-Frenkel Foundation; Human Frontier Science Program (HFSP) Career Development Award HFSP [CDA00014/2012]; European Research Council [ERC-2011 METACYCLES 310320]
PY - 2016/3/22
Y1 - 2016/3/22
N2 - Mitochondria are major suppliers of cellular energy through nutrients oxidation. Little is known about the mechanisms that enable mitochondria to cope with changes in nutrient supply and energy demand that naturally occur throughout the day. To address this question, we applied MS-based quantitative proteomics on isolated mitochondria from mice killed throughout the day and identified extensive oscillations in the mitochondrial proteome. Remarkably, the majority of cycling mitochondrial proteins peaked during the early light phase. We found that rate-limiting mitochondrial enzymes that process lipids and carbohydrates accumulate in a diurnal manner and are dependent on the clock proteins PER1/2. In this conjuncture, we uncovered daily oscillations in mitochondrial respiration that peak during different times of the day in response to different nutrients. Notably, the diurnal regulation of mitochondrial respiration was blunted in mice lacking PER1/2 or on a high-fat diet. We propose that PERIOD proteins optimize mitochondrial metabolism to daily changes in energy supply/demand and thereby, serve as a rheostat for mitochondrial nutrient utilization.
AB - Mitochondria are major suppliers of cellular energy through nutrients oxidation. Little is known about the mechanisms that enable mitochondria to cope with changes in nutrient supply and energy demand that naturally occur throughout the day. To address this question, we applied MS-based quantitative proteomics on isolated mitochondria from mice killed throughout the day and identified extensive oscillations in the mitochondrial proteome. Remarkably, the majority of cycling mitochondrial proteins peaked during the early light phase. We found that rate-limiting mitochondrial enzymes that process lipids and carbohydrates accumulate in a diurnal manner and are dependent on the clock proteins PER1/2. In this conjuncture, we uncovered daily oscillations in mitochondrial respiration that peak during different times of the day in response to different nutrients. Notably, the diurnal regulation of mitochondrial respiration was blunted in mice lacking PER1/2 or on a high-fat diet. We propose that PERIOD proteins optimize mitochondrial metabolism to daily changes in energy supply/demand and thereby, serve as a rheostat for mitochondrial nutrient utilization.
KW - Circadian rhythm
KW - Metabolism
KW - Mitochondria
KW - PERIOD proteins
KW - Proteomics
UR - http://www.scopus.com/inward/record.url?scp=84962311227&partnerID=8YFLogxK
U2 - 10.1073/pnas.1519650113
DO - 10.1073/pnas.1519650113
M3 - مقالة
C2 - 26862173
SN - 0027-8424
VL - 113
SP - E1673-E1682
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 12
ER -