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Casein kinase 1 dynamics underlie substrate selectivity and the PER2 circadian phosphoswitch

Post-translational control of PERIOD stability by Casein Kinase 1δ and ε (CK1) plays a key regulatory role in metazoan circadian rhythms. Despite the deep evolutionary conservation of CK1 in eukaryotes, little is known about its regulation and the factors that influence substrate selectivity on func...

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Autores principales: Philpott, Jonathan M, Narasimamurthy, Rajesh, Ricci, Clarisse G, Freeberg, Alfred M, Hunt, Sabrina R, Yee, Lauren E, Pelofsky, Rebecca S, Tripathi, Sarvind, Virshup, David M, Partch, Carrie L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012598/
https://www.ncbi.nlm.nih.gov/pubmed/32043967
http://dx.doi.org/10.7554/eLife.52343
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author Philpott, Jonathan M
Narasimamurthy, Rajesh
Ricci, Clarisse G
Freeberg, Alfred M
Hunt, Sabrina R
Yee, Lauren E
Pelofsky, Rebecca S
Tripathi, Sarvind
Virshup, David M
Partch, Carrie L
author_facet Philpott, Jonathan M
Narasimamurthy, Rajesh
Ricci, Clarisse G
Freeberg, Alfred M
Hunt, Sabrina R
Yee, Lauren E
Pelofsky, Rebecca S
Tripathi, Sarvind
Virshup, David M
Partch, Carrie L
author_sort Philpott, Jonathan M
collection PubMed
description Post-translational control of PERIOD stability by Casein Kinase 1δ and ε (CK1) plays a key regulatory role in metazoan circadian rhythms. Despite the deep evolutionary conservation of CK1 in eukaryotes, little is known about its regulation and the factors that influence substrate selectivity on functionally antagonistic sites in PERIOD that directly control circadian period. Here we describe a molecular switch involving a highly conserved anion binding site in CK1. This switch controls conformation of the kinase activation loop and determines which sites on mammalian PER2 are preferentially phosphorylated, thereby directly regulating PER2 stability. Integrated experimental and computational studies shed light on the allosteric linkage between two anion binding sites that dynamically regulate kinase activity. We show that period-altering kinase mutations from humans to Drosophila differentially modulate this activation loop switch to elicit predictable changes in PER2 stability, providing a foundation to understand and further manipulate CK1 regulation of circadian rhythms.
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spelling pubmed-70125982020-02-12 Casein kinase 1 dynamics underlie substrate selectivity and the PER2 circadian phosphoswitch Philpott, Jonathan M Narasimamurthy, Rajesh Ricci, Clarisse G Freeberg, Alfred M Hunt, Sabrina R Yee, Lauren E Pelofsky, Rebecca S Tripathi, Sarvind Virshup, David M Partch, Carrie L eLife Structural Biology and Molecular Biophysics Post-translational control of PERIOD stability by Casein Kinase 1δ and ε (CK1) plays a key regulatory role in metazoan circadian rhythms. Despite the deep evolutionary conservation of CK1 in eukaryotes, little is known about its regulation and the factors that influence substrate selectivity on functionally antagonistic sites in PERIOD that directly control circadian period. Here we describe a molecular switch involving a highly conserved anion binding site in CK1. This switch controls conformation of the kinase activation loop and determines which sites on mammalian PER2 are preferentially phosphorylated, thereby directly regulating PER2 stability. Integrated experimental and computational studies shed light on the allosteric linkage between two anion binding sites that dynamically regulate kinase activity. We show that period-altering kinase mutations from humans to Drosophila differentially modulate this activation loop switch to elicit predictable changes in PER2 stability, providing a foundation to understand and further manipulate CK1 regulation of circadian rhythms. eLife Sciences Publications, Ltd 2020-02-11 /pmc/articles/PMC7012598/ /pubmed/32043967 http://dx.doi.org/10.7554/eLife.52343 Text en © 2020, Philpott et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Structural Biology and Molecular Biophysics
Philpott, Jonathan M
Narasimamurthy, Rajesh
Ricci, Clarisse G
Freeberg, Alfred M
Hunt, Sabrina R
Yee, Lauren E
Pelofsky, Rebecca S
Tripathi, Sarvind
Virshup, David M
Partch, Carrie L
Casein kinase 1 dynamics underlie substrate selectivity and the PER2 circadian phosphoswitch
title Casein kinase 1 dynamics underlie substrate selectivity and the PER2 circadian phosphoswitch
title_full Casein kinase 1 dynamics underlie substrate selectivity and the PER2 circadian phosphoswitch
title_fullStr Casein kinase 1 dynamics underlie substrate selectivity and the PER2 circadian phosphoswitch
title_full_unstemmed Casein kinase 1 dynamics underlie substrate selectivity and the PER2 circadian phosphoswitch
title_short Casein kinase 1 dynamics underlie substrate selectivity and the PER2 circadian phosphoswitch
title_sort casein kinase 1 dynamics underlie substrate selectivity and the per2 circadian phosphoswitch
topic Structural Biology and Molecular Biophysics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012598/
https://www.ncbi.nlm.nih.gov/pubmed/32043967
http://dx.doi.org/10.7554/eLife.52343
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