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Integrated omics in Drosophila uncover a circadian kinome
Most organisms on the earth exhibit circadian rhythms in behavior and physiology, which are driven by endogenous clocks. Phosphorylation plays a central role in timing the clock, but how this contributes to overt rhythms is unclear. Here we conduct phosphoproteomics in conjunction with transcriptomi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264355/ https://www.ncbi.nlm.nih.gov/pubmed/32483184 http://dx.doi.org/10.1038/s41467-020-16514-z |
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author | Wang, Chenwei Shui, Ke Ma, Shanshan Lin, Shaofeng Zhang, Ying Wen, Bo Deng, Wankun Xu, Haodong Hu, Hui Guo, Anyuan Xue, Yu Zhang, Luoying |
author_facet | Wang, Chenwei Shui, Ke Ma, Shanshan Lin, Shaofeng Zhang, Ying Wen, Bo Deng, Wankun Xu, Haodong Hu, Hui Guo, Anyuan Xue, Yu Zhang, Luoying |
author_sort | Wang, Chenwei |
collection | PubMed |
description | Most organisms on the earth exhibit circadian rhythms in behavior and physiology, which are driven by endogenous clocks. Phosphorylation plays a central role in timing the clock, but how this contributes to overt rhythms is unclear. Here we conduct phosphoproteomics in conjunction with transcriptomic and proteomic profiling using fly heads. By developing a pipeline for integrating multi-omics data, we identify 789 (~17%) phosphorylation sites with circadian oscillations. We predict 27 potential circadian kinases to participate in phosphorylating these sites, including 7 previously known to function in the clock. We screen the remaining 20 kinases for effects on circadian rhythms and find an additional 3 to be involved in regulating locomotor rhythm. We re-construct a signal web that includes the 10 circadian kinases and identify GASKET as a potentially important regulator. Taken together, we uncover a circadian kinome that potentially shapes the temporal pattern of the entire circadian molecular landscapes. |
format | Online Article Text |
id | pubmed-7264355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72643552020-06-12 Integrated omics in Drosophila uncover a circadian kinome Wang, Chenwei Shui, Ke Ma, Shanshan Lin, Shaofeng Zhang, Ying Wen, Bo Deng, Wankun Xu, Haodong Hu, Hui Guo, Anyuan Xue, Yu Zhang, Luoying Nat Commun Article Most organisms on the earth exhibit circadian rhythms in behavior and physiology, which are driven by endogenous clocks. Phosphorylation plays a central role in timing the clock, but how this contributes to overt rhythms is unclear. Here we conduct phosphoproteomics in conjunction with transcriptomic and proteomic profiling using fly heads. By developing a pipeline for integrating multi-omics data, we identify 789 (~17%) phosphorylation sites with circadian oscillations. We predict 27 potential circadian kinases to participate in phosphorylating these sites, including 7 previously known to function in the clock. We screen the remaining 20 kinases for effects on circadian rhythms and find an additional 3 to be involved in regulating locomotor rhythm. We re-construct a signal web that includes the 10 circadian kinases and identify GASKET as a potentially important regulator. Taken together, we uncover a circadian kinome that potentially shapes the temporal pattern of the entire circadian molecular landscapes. Nature Publishing Group UK 2020-06-01 /pmc/articles/PMC7264355/ /pubmed/32483184 http://dx.doi.org/10.1038/s41467-020-16514-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Chenwei Shui, Ke Ma, Shanshan Lin, Shaofeng Zhang, Ying Wen, Bo Deng, Wankun Xu, Haodong Hu, Hui Guo, Anyuan Xue, Yu Zhang, Luoying Integrated omics in Drosophila uncover a circadian kinome |
title | Integrated omics in Drosophila uncover a circadian kinome |
title_full | Integrated omics in Drosophila uncover a circadian kinome |
title_fullStr | Integrated omics in Drosophila uncover a circadian kinome |
title_full_unstemmed | Integrated omics in Drosophila uncover a circadian kinome |
title_short | Integrated omics in Drosophila uncover a circadian kinome |
title_sort | integrated omics in drosophila uncover a circadian kinome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264355/ https://www.ncbi.nlm.nih.gov/pubmed/32483184 http://dx.doi.org/10.1038/s41467-020-16514-z |
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