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The Emergence of Circadian Timekeeping in the Intestine
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AbstractThe circadian clock is a molecular timekeeper, present from cyanobacteria to mammals, that coordinates internal physiology with the external environment. The clock has a 24-hour period however development proceeds with its own timing, raising the question of how these interact. Using the intestine ofDrosophila melanogasteras a model for organ development, we track how and when the circadian clock emerges in specific cell types. We find that the circadian clock begins abruptly in the adult intestine and gradually synchronizes to the environment after intestinal development is complete. This delayed start occurs because individual cells at earlier stages lack the complete circadian clock gene network. As the intestine develops, the circadian clock is first consolidated in intestinal stem cells with changes in ecdysone and Bursicon hormone signalling influencing the transcriptional activity of Clk/cyc to drive the expression oftim,Pdp1,andvri. In the mature intestine, stem cell lineage commitment transiently disrupts clock activity in differentiating progeny, mirroring early developmental clock-less transitions. Our data show that clock function and differentiation are incompatible and provide a paradigm for studying circadian clocks in development and stem cell lineages.
Cold Spring Harbor Laboratory
Title: The Emergence of Circadian Timekeeping in the Intestine
Description:
AbstractThe circadian clock is a molecular timekeeper, present from cyanobacteria to mammals, that coordinates internal physiology with the external environment.
The clock has a 24-hour period however development proceeds with its own timing, raising the question of how these interact.
Using the intestine ofDrosophila melanogasteras a model for organ development, we track how and when the circadian clock emerges in specific cell types.
We find that the circadian clock begins abruptly in the adult intestine and gradually synchronizes to the environment after intestinal development is complete.
This delayed start occurs because individual cells at earlier stages lack the complete circadian clock gene network.
As the intestine develops, the circadian clock is first consolidated in intestinal stem cells with changes in ecdysone and Bursicon hormone signalling influencing the transcriptional activity of Clk/cyc to drive the expression oftim,Pdp1,andvri.
In the mature intestine, stem cell lineage commitment transiently disrupts clock activity in differentiating progeny, mirroring early developmental clock-less transitions.
Our data show that clock function and differentiation are incompatible and provide a paradigm for studying circadian clocks in development and stem cell lineages.
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