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Circadian period is compensated for repressor protein turnover rates in single cells.


ABSTRACT: Most mammalian cells have molecular circadian clocks that generate widespread rhythms in transcript and protein abundance. While circadian clocks are robust to fluctuations in the cellular environment, little is known about the mechanisms by which the circadian period compensates for fluctuating metabolic states. Here, we exploit the heterogeneity of single cells both in circadian period and a metabolic parameter-protein stability-to study their interdependence without the need for genetic manipulation. We generated cells expressing key circadian proteins (CRYPTOCHROME1/2 (CRY1/2) and PERIOD1/2 (PER1/2)) as endogenous fusions with fluorescent proteins and simultaneously monitored circadian rhythms and degradation in thousands of single cells. We found that the circadian period compensates for fluctuations in the turnover rates of circadian repressor proteins and uncovered possible mechanisms using a mathematical model. In addition, the stabilities of the repressor proteins are circadian phase dependent and correlate with the circadian period in a phase-dependent manner, in contrast to the prevailing model.

SUBMITTER: Gabriel CH 

PROVIDER: S-EPMC11348271 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature

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Circadian period is compensated for repressor protein turnover rates in single cells.

Gabriel Christian H CH   Del Olmo Marta M   Rizki Widini Arunya A   Roshanbin Rashin R   Woyde Jonas J   Hamza Ebrahim E   Gutu Nica-Nicoleta NN   Zehtabian Amin A   Ewers Helge H   Granada Adrian A   Herzel Hanspeter H   Kramer Achim A  

Proceedings of the National Academy of Sciences of the United States of America 20240814 34


Most mammalian cells have molecular circadian clocks that generate widespread rhythms in transcript and protein abundance. While circadian clocks are robust to fluctuations in the cellular environment, little is known about the mechanisms by which the circadian period compensates for fluctuating metabolic states. Here, we exploit the heterogeneity of single cells both in circadian period and a metabolic parameter-protein stability-to study their interdependence without the need for genetic manip  ...[more]

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