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Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity

The time of day strongly influences adaptive behaviors like long-term memory, but the correlating synaptic and molecular mechanisms remain unclear. The circadian clock comprises a canonical transcription-translation feedback loop (TTFL) strictly dependent on the BMAL1 transcription factor. We report...

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Autores principales: Barone, Ilaria, Gilette, Nicole M., Hawks-Mayer, Hannah, Handy, Jonathan, Zhang, Kevin J., Chifamba, Fortunate F., Mostafa, Engie, Johnson-Venkatesh, Erin M., Sun, Yan, Gibson, Jennifer M., Rotenberg, Alexander, Umemori, Hisashi, Tsai, Peter T., Lipton, Jonathan O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599629/
https://www.ncbi.nlm.nih.gov/pubmed/37878694
http://dx.doi.org/10.1126/sciadv.adj1010
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author Barone, Ilaria
Gilette, Nicole M.
Hawks-Mayer, Hannah
Handy, Jonathan
Zhang, Kevin J.
Chifamba, Fortunate F.
Mostafa, Engie
Johnson-Venkatesh, Erin M.
Sun, Yan
Gibson, Jennifer M.
Rotenberg, Alexander
Umemori, Hisashi
Tsai, Peter T.
Lipton, Jonathan O.
author_facet Barone, Ilaria
Gilette, Nicole M.
Hawks-Mayer, Hannah
Handy, Jonathan
Zhang, Kevin J.
Chifamba, Fortunate F.
Mostafa, Engie
Johnson-Venkatesh, Erin M.
Sun, Yan
Gibson, Jennifer M.
Rotenberg, Alexander
Umemori, Hisashi
Tsai, Peter T.
Lipton, Jonathan O.
author_sort Barone, Ilaria
collection PubMed
description The time of day strongly influences adaptive behaviors like long-term memory, but the correlating synaptic and molecular mechanisms remain unclear. The circadian clock comprises a canonical transcription-translation feedback loop (TTFL) strictly dependent on the BMAL1 transcription factor. We report that BMAL1 rhythmically localizes to hippocampal synapses in a manner dependent on its phosphorylation at Ser(42) [pBMAL1(S42)]. pBMAL1(S42) regulates the autophosphorylation of synaptic CaMKIIα and circadian rhythms of CaMKIIα-dependent molecular interactions and LTP but not global rest/activity behavior. Therefore, our results suggest a model in which repurposing of the clock protein BMAL1 to synapses locally gates the circadian timing of plasticity.
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spelling pubmed-105996292023-10-26 Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity Barone, Ilaria Gilette, Nicole M. Hawks-Mayer, Hannah Handy, Jonathan Zhang, Kevin J. Chifamba, Fortunate F. Mostafa, Engie Johnson-Venkatesh, Erin M. Sun, Yan Gibson, Jennifer M. Rotenberg, Alexander Umemori, Hisashi Tsai, Peter T. Lipton, Jonathan O. Sci Adv Neuroscience The time of day strongly influences adaptive behaviors like long-term memory, but the correlating synaptic and molecular mechanisms remain unclear. The circadian clock comprises a canonical transcription-translation feedback loop (TTFL) strictly dependent on the BMAL1 transcription factor. We report that BMAL1 rhythmically localizes to hippocampal synapses in a manner dependent on its phosphorylation at Ser(42) [pBMAL1(S42)]. pBMAL1(S42) regulates the autophosphorylation of synaptic CaMKIIα and circadian rhythms of CaMKIIα-dependent molecular interactions and LTP but not global rest/activity behavior. Therefore, our results suggest a model in which repurposing of the clock protein BMAL1 to synapses locally gates the circadian timing of plasticity. American Association for the Advancement of Science 2023-10-25 /pmc/articles/PMC10599629/ /pubmed/37878694 http://dx.doi.org/10.1126/sciadv.adj1010 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Neuroscience
Barone, Ilaria
Gilette, Nicole M.
Hawks-Mayer, Hannah
Handy, Jonathan
Zhang, Kevin J.
Chifamba, Fortunate F.
Mostafa, Engie
Johnson-Venkatesh, Erin M.
Sun, Yan
Gibson, Jennifer M.
Rotenberg, Alexander
Umemori, Hisashi
Tsai, Peter T.
Lipton, Jonathan O.
Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity
title Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity
title_full Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity
title_fullStr Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity
title_full_unstemmed Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity
title_short Synaptic BMAL1 phosphorylation controls circadian hippocampal plasticity
title_sort synaptic bmal1 phosphorylation controls circadian hippocampal plasticity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599629/
https://www.ncbi.nlm.nih.gov/pubmed/37878694
http://dx.doi.org/10.1126/sciadv.adj1010
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