Sleep-wake cycles drive daily dynamics of synaptic phosphorylation
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Sleep-wake cycles drive daily dynamics of synaptic phosphorylation. / Brüning, Franziska; Noya, Sara B; Bange, Tanja; Koutsouli, Stella; Rudolph, Jan D; Tyagarajan, Shiva K; Cox, Jürgen; Mann, Matthias; Brown, Steven A; Robles, Maria S.
In: Science (New York, N.Y.), Vol. 366, No. 6462, eaav3617 , 2019.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Sleep-wake cycles drive daily dynamics of synaptic phosphorylation
AU - Brüning, Franziska
AU - Noya, Sara B
AU - Bange, Tanja
AU - Koutsouli, Stella
AU - Rudolph, Jan D
AU - Tyagarajan, Shiva K
AU - Cox, Jürgen
AU - Mann, Matthias
AU - Brown, Steven A
AU - Robles, Maria S
PY - 2019
Y1 - 2019
N2 - The circadian clock drives daily changes of physiology, including sleep-wake cycles, through regulation of transcription, protein abundance, and function. Circadian phosphorylation controls cellular processes in peripheral organs, but little is known about its role in brain function and synaptic activity. We applied advanced quantitative phosphoproteomics to mouse forebrain synaptoneurosomes isolated across 24 hours, accurately quantifying almost 8000 phosphopeptides. Half of the synaptic phosphoproteins, including numerous kinases, had large-amplitude rhythms peaking at rest-activity and activity-rest transitions. Bioinformatic analyses revealed global temporal control of synaptic function through phosphorylation, including synaptic transmission, cytoskeleton reorganization, and excitatory/inhibitory balance. Sleep deprivation abolished 98% of all phosphorylation cycles in synaptoneurosomes, indicating that sleep-wake cycles rather than circadian signals are main drivers of synaptic phosphorylation, responding to both sleep and wake pressures.
AB - The circadian clock drives daily changes of physiology, including sleep-wake cycles, through regulation of transcription, protein abundance, and function. Circadian phosphorylation controls cellular processes in peripheral organs, but little is known about its role in brain function and synaptic activity. We applied advanced quantitative phosphoproteomics to mouse forebrain synaptoneurosomes isolated across 24 hours, accurately quantifying almost 8000 phosphopeptides. Half of the synaptic phosphoproteins, including numerous kinases, had large-amplitude rhythms peaking at rest-activity and activity-rest transitions. Bioinformatic analyses revealed global temporal control of synaptic function through phosphorylation, including synaptic transmission, cytoskeleton reorganization, and excitatory/inhibitory balance. Sleep deprivation abolished 98% of all phosphorylation cycles in synaptoneurosomes, indicating that sleep-wake cycles rather than circadian signals are main drivers of synaptic phosphorylation, responding to both sleep and wake pressures.
U2 - 10.1126/science.aav3617
DO - 10.1126/science.aav3617
M3 - Journal article
C2 - 31601740
VL - 366
JO - Science
JF - Science
SN - 0036-8075
IS - 6462
M1 - eaav3617
ER -
ID: 229855784