TY - JOUR
T1 - Translation-independent circadian control of the cell cycle in a unicellular photosynthetic eukaryote
AU - Miyagishima, Shin Ya
AU - Fujiwara, Takayuki
AU - Sumiya, Nobuko
AU - Hirooka, Shunsuke
AU - Nakano, Akihiko
AU - Kabeya, Yukihiro
AU - Nakamura, Mami
N1 - Funding Information:
We thank A. Yamashita for technical support and K. Fukaya and BSI’s Research Resources Center of RIKEN for LC-MS/MS analyses. This study was supported by Grant-in-Aid for Scientific Research from Japan Society for the Promotion of Science (no. 19870033 to S.-y.M.) and by Core Research for Evolutional Science and Technology (CREST) Program of Japan Science and Technology Agency (JST) (to S.-y.M.).
PY - 2014/5/8
Y1 - 2014/5/8
N2 - Circadian rhythms of cell division have been observed in several lineages of eukaryotes, especially photosynthetic unicellular eukaryotes. However, the mechanism underlying the circadian regulation of the cell cycle and the nature of the advantage conferred remain unknown. Here, using the unicellular red alga Cyanidioschyzon merolae, we show that the G1/S regulator RBR-E2F-DP complex links the G1/S transition to circadian rhythms. Time-dependent E2F phosphorylation promotes the G1/S transition during subjective night and this phosphorylation event occurs independently of cell cycle progression, even under continuous dark or when cytosolic translation is inhibited. Constitutive expression of a phospho-mimic of E2F or depletion of RBR unlinks cell cycle progression from circadian rhythms. These transgenic lines are exposed to higher oxidative stress than the wild type. Circadian inhibition of cell cycle progression during the daytime by RBR-E2F-DP pathway likely protects cells from photosynthetic oxidative stress by temporally compartmentalizing photosynthesis and cell cycle progression.
AB - Circadian rhythms of cell division have been observed in several lineages of eukaryotes, especially photosynthetic unicellular eukaryotes. However, the mechanism underlying the circadian regulation of the cell cycle and the nature of the advantage conferred remain unknown. Here, using the unicellular red alga Cyanidioschyzon merolae, we show that the G1/S regulator RBR-E2F-DP complex links the G1/S transition to circadian rhythms. Time-dependent E2F phosphorylation promotes the G1/S transition during subjective night and this phosphorylation event occurs independently of cell cycle progression, even under continuous dark or when cytosolic translation is inhibited. Constitutive expression of a phospho-mimic of E2F or depletion of RBR unlinks cell cycle progression from circadian rhythms. These transgenic lines are exposed to higher oxidative stress than the wild type. Circadian inhibition of cell cycle progression during the daytime by RBR-E2F-DP pathway likely protects cells from photosynthetic oxidative stress by temporally compartmentalizing photosynthesis and cell cycle progression.
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U2 - 10.1038/ncomms4807
DO - 10.1038/ncomms4807
M3 - Article
C2 - 24806410
AN - SCOPUS:84900002941
SN - 2041-1723
VL - 5
JO - Nature communications
JF - Nature communications
M1 - 3807
ER -