Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783496256865173504 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7012598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT philpottjonathanm caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT narasimamurthyrajesh caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT ricciclarisseg caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT freebergalfredm caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT huntsabrinar caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT yeelaurene caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT pelofskyrebeccas caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT tripathisarvind caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT virshupdavidm caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch AT partchcarriel caseinkinase1dynamicsunderliesubstrateselectivityandtheper2circadianphosphoswitch |