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PERIOD Phosphoclusters Control Temperature Compensation of the Drosophila Circadian Clock
Ambient temperature varies constantly. However, the period of circadian pacemakers is remarkably stable over a wide-range of ecologically- and physiologically-relevant temperatures, even though the kinetics of most biochemical reactions accelerates as temperature rises. This thermal buffering phenom...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201207/ https://www.ncbi.nlm.nih.gov/pubmed/35721569 http://dx.doi.org/10.3389/fphys.2022.888262 |
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author | Joshi, Radhika Cai, Yao D. Xia, Yongliang Chiu, Joanna C. Emery, Patrick |
author_facet | Joshi, Radhika Cai, Yao D. Xia, Yongliang Chiu, Joanna C. Emery, Patrick |
author_sort | Joshi, Radhika |
collection | PubMed |
description | Ambient temperature varies constantly. However, the period of circadian pacemakers is remarkably stable over a wide-range of ecologically- and physiologically-relevant temperatures, even though the kinetics of most biochemical reactions accelerates as temperature rises. This thermal buffering phenomenon, called temperature compensation, is a critical feature of circadian rhythms, but how it is achieved remains elusive. Here, we uncovered the important role played by the Drosophila PERIOD (PER) phosphodegron in temperature compensation. This phosphorylation hotspot is crucial for PER proteasomal degradation and is the functional homolog of mammalian PER2 S478 phosphodegron, which also impacts temperature compensation. Using CRISPR-Cas9, we introduced a series of mutations that altered three Serines of the PER phosphodegron. While all three Serine to Alanine substitutions lengthened period at all temperatures tested, temperature compensation was differentially affected. S44A and S45A substitutions caused undercompensation, while S47A resulted in overcompensation. These results thus reveal unexpected functional heterogeneity of phosphodegron residues in thermal compensation. Furthermore, mutations impairing phosphorylation of the per ( s ) phosphocluster showed undercompensation, consistent with its inhibitory role on S47 phosphorylation. We observed that S47A substitution caused increased accumulation of hyper-phosphorylated PER at warmer temperatures. This finding was corroborated by cell culture assays in which S47A slowed down phosphorylation-dependent PER degradation at high temperatures, causing PER degradation to be excessively temperature-compensated. Thus, our results point to a novel role of the PER phosphodegron in temperature compensation through temperature-dependent modulation of the abundance of hyper-phosphorylated PER. Our work reveals interesting mechanistic convergences and differences between mammalian and Drosophila temperature compensation of the circadian clock. |
format | Online Article Text |
id | pubmed-9201207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92012072022-06-17 PERIOD Phosphoclusters Control Temperature Compensation of the Drosophila Circadian Clock Joshi, Radhika Cai, Yao D. Xia, Yongliang Chiu, Joanna C. Emery, Patrick Front Physiol Physiology Ambient temperature varies constantly. However, the period of circadian pacemakers is remarkably stable over a wide-range of ecologically- and physiologically-relevant temperatures, even though the kinetics of most biochemical reactions accelerates as temperature rises. This thermal buffering phenomenon, called temperature compensation, is a critical feature of circadian rhythms, but how it is achieved remains elusive. Here, we uncovered the important role played by the Drosophila PERIOD (PER) phosphodegron in temperature compensation. This phosphorylation hotspot is crucial for PER proteasomal degradation and is the functional homolog of mammalian PER2 S478 phosphodegron, which also impacts temperature compensation. Using CRISPR-Cas9, we introduced a series of mutations that altered three Serines of the PER phosphodegron. While all three Serine to Alanine substitutions lengthened period at all temperatures tested, temperature compensation was differentially affected. S44A and S45A substitutions caused undercompensation, while S47A resulted in overcompensation. These results thus reveal unexpected functional heterogeneity of phosphodegron residues in thermal compensation. Furthermore, mutations impairing phosphorylation of the per ( s ) phosphocluster showed undercompensation, consistent with its inhibitory role on S47 phosphorylation. We observed that S47A substitution caused increased accumulation of hyper-phosphorylated PER at warmer temperatures. This finding was corroborated by cell culture assays in which S47A slowed down phosphorylation-dependent PER degradation at high temperatures, causing PER degradation to be excessively temperature-compensated. Thus, our results point to a novel role of the PER phosphodegron in temperature compensation through temperature-dependent modulation of the abundance of hyper-phosphorylated PER. Our work reveals interesting mechanistic convergences and differences between mammalian and Drosophila temperature compensation of the circadian clock. Frontiers Media S.A. 2022-06-02 /pmc/articles/PMC9201207/ /pubmed/35721569 http://dx.doi.org/10.3389/fphys.2022.888262 Text en Copyright © 2022 Joshi, Cai, Xia, Chiu and Emery. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Joshi, Radhika Cai, Yao D. Xia, Yongliang Chiu, Joanna C. Emery, Patrick PERIOD Phosphoclusters Control Temperature Compensation of the Drosophila Circadian Clock |
title | PERIOD Phosphoclusters Control Temperature Compensation of the Drosophila Circadian Clock |
title_full | PERIOD Phosphoclusters Control Temperature Compensation of the Drosophila Circadian Clock |
title_fullStr | PERIOD Phosphoclusters Control Temperature Compensation of the Drosophila Circadian Clock |
title_full_unstemmed | PERIOD Phosphoclusters Control Temperature Compensation of the Drosophila Circadian Clock |
title_short | PERIOD Phosphoclusters Control Temperature Compensation of the Drosophila Circadian Clock |
title_sort | period phosphoclusters control temperature compensation of the drosophila circadian clock |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201207/ https://www.ncbi.nlm.nih.gov/pubmed/35721569 http://dx.doi.org/10.3389/fphys.2022.888262 |
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