Author
Listed:
- Kumiko Yoshioka-Kobayashi
(Kyoto University
Kyoto University)
- Marina Matsumiya
(Kyoto University
Kyoto University)
- Yusuke Niino
(RIKEN Center for Brain Science)
- Akihiro Isomura
(Kyoto University
Japan Science and Technology Agency
Kyoto University)
- Hiroshi Kori
(The University of Tokyo)
- Atsushi Miyawaki
(RIKEN Center for Brain Science
RIKEN Center for Advanced Photonics)
- Ryoichiro Kageyama
(Kyoto University
Kyoto University
Kyoto University
Kyoto University)
Abstract
Individual cellular activities fluctuate but are constantly coordinated at the population level via cell–cell coupling. A notable example is the somite segmentation clock, in which the expression of clock genes (such as Hes7) oscillates in synchrony between the cells that comprise the presomitic mesoderm (PSM)1,2. This synchronization depends on the Notch signalling pathway; inhibiting this pathway desynchronizes oscillations, leading to somite fusion3–7. However, how Notch signalling regulates the synchronicity of HES7 oscillations is unknown. Here we establish a live-imaging system using a new fluorescent reporter (Achilles), which we fuse with HES7 to monitor synchronous oscillations in HES7 expression in the mouse PSM at a single-cell resolution. Wild-type cells can rapidly correct for phase fluctuations in HES7 oscillations, whereas the absence of the Notch modulator gene lunatic fringe (Lfng) leads to a loss of synchrony between PSM cells. Furthermore, HES7 oscillations are severely dampened in individual cells of Lfng-null PSM. However, when Lfng-null PSM cells were completely dissociated, the amplitude and periodicity of HES7 oscillations were almost normal, which suggests that LFNG is involved mostly in cell–cell coupling. Mixed cultures of control and Lfng-null PSM cells, and an optogenetic Notch signalling reporter assay, revealed that LFNG delays the signal-sending process of intercellular Notch signalling transmission. These results—together with mathematical modelling—raised the possibility that Lfng-null PSM cells shorten the coupling delay, thereby approaching a condition known as the oscillation or amplitude death of coupled oscillators8. Indeed, a small compound that lengthens the coupling delay partially rescues the amplitude and synchrony of HES7 oscillations in Lfng-null PSM cells. Our study reveals a delay control mechanism of the oscillatory networks involved in somite segmentation, and indicates that intercellular coupling with the correct delay is essential for synchronized oscillation.
Suggested Citation
Kumiko Yoshioka-Kobayashi & Marina Matsumiya & Yusuke Niino & Akihiro Isomura & Hiroshi Kori & Atsushi Miyawaki & Ryoichiro Kageyama, 2020.
"Coupling delay controls synchronized oscillation in the segmentation clock,"
Nature, Nature, vol. 580(7801), pages 119-123, April.
Handle:
RePEc:nat:nature:v:580:y:2020:i:7801:d:10.1038_s41586-019-1882-z
DOI: 10.1038/s41586-019-1882-z
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Citations
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Cited by:
- Taijiro Yabe & Koichiro Uriu & Shinji Takada, 2023.
"Ripply suppresses Tbx6 to induce dynamic-to-static conversion in somite segmentation,"
Nature Communications, Nature, vol. 14(1), pages 1-18, December.
- Yukinari Haraoka & Yuki Akieda & Yuri Nagai & Chihiro Mogi & Tohru Ishitani, 2022.
"Zebrafish imaging reveals TP53 mutation switching oncogene-induced senescence from suppressor to driver in primary tumorigenesis,"
Nature Communications, Nature, vol. 13(1), pages 1-15, December.
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