4.7 Article

The Circadian Clock Gene Circuit Controls Protein and Phosphoprotein Rhythms in Arabidopsis thaliana

Journal

MOLECULAR & CELLULAR PROTEOMICS
Volume 21, Issue 1, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.mcpro.2021.100172

Keywords

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Funding

  1. Wellcome Trust [096995/Z/11/Z]
  2. BBSRC [BB/D019621, BB/J009423]
  3. Wellcome Trust [096995/Z/11/Z] Funding Source: Wellcome Trust

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This study observed the proteomic and phosphoproteomic time series of Arabidopsis thaliana plants under constant light conditions. It found that only a small percentage of proteins and a larger proportion of phospho-sites exhibited rhythmic changes. Furthermore, half of the rhythmic phospho-sites showed the highest phosphorylation levels at subjective dawn. The clock gene circuit plays a crucial role in most protein phosphorylation rhythms, but not necessarily in all of them.
Twenty-four-hour, circadian rhythms control many eukaryotic mRNA levels, whereas the levels of their more stable proteins are not expected to reflect the RNA rhythms, emphasizing the need to test the circadian regulation of protein abundance and modification. Here we present circadian proteomic and phosphoproteomic time series from Arabidopsis thaliana plants under constant light conditions, estimating that just 0.4% of quantified proteins but a much larger proportion of quantified phospho-sites were rhythmic. Approximately half of the rhythmic phospho-sites were most phosphorylated at subjective dawn, a pattern we term the phospho-dawn. Members of the SnRK/CDPK family of protein kinases are candidate regulators. A CCA1-overexpressing line that disables the clock gene circuit lacked most circadian protein phosphorylation. However, the few phospho-sites that fluctuated despite CCA1-overexpression still tended to peak in abundance close to subjective dawn, suggesting that the canonical clock mechanism is necessary for most but perhaps not all protein phosphorylation rhythms. To test the potential functional relevance of our datasets, we conducted phosphomimetic experiments using the bifunctional enzyme fructose-6-phosphate-2-kinase/ phosphatase (F2KP), as an example. The rhythmic phosphorylation of diverse protein targets is controlled by the clock gene circuit, implicating posttranslational mechanisms in the transmission of circadian timing information in plants.

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