1. Academic Validation
  2. Collective oscillatory signaling in Dictyosteliumdiscoideum acts as a developmental timer initiated by weak coupling of a noisy pulsatile signal

Collective oscillatory signaling in Dictyosteliumdiscoideum acts as a developmental timer initiated by weak coupling of a noisy pulsatile signal

  • Dev Cell. 2024 Dec 5:S1534-5807(24)00698-1. doi: 10.1016/j.devcel.2024.11.016.
Christopher A Brimson 1 Robert Baines 1 Elisabeth Sams-Dodd 1 Ioanina Stefanescu 1 Bethany Evans 1 Satoshi Kuwana 2 Hidenori Hashimura 2 Satoshi Sawai 2 Christopher R L Thompson 3
Affiliations

Affiliations

  • 1 Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK.
  • 2 Graduate School of Arts and Sciences, University of Tokyo, Komaba, Meguro-ku, Tokyo, Japan.
  • 3 Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK. Electronic address: christopher.thompson@ucl.ac.uk.
Abstract

Oscillatory phenomena play widespread roles in the control of biological systems. In D. discoideum, oscillatory cyclic adenosine monophosphate (cAMP) signaling drives collective behavior and induces a temporal developmental gene expression program. How collective cAMP oscillations emerge or how they encode temporal transcriptional information is still poorly understood. To address this, we identified a transcription factor required for the initiation of collective behavior. Hbx5 activity is cAMP dependent and provides a sensitive single-cell readout for cAMP signaling. Extensive stochastic pulsatile cAMP signaling is found to precede collective oscillations. Stochastic signaling induces Hbx5-dependent transcriptional feedback, which enhances signal sensitivity and cell-cell coupling. This results in the emergence of synchronized collective oscillations, which subsequently activates the GtaC transcription factor and triggers shifts in developmental gene expression. Our results suggest this temporal coordination is encoded by changes in the amplitude of cAMP oscillations and differential sensitivity of these transcription factors to the cAMP-regulated kinase ErkB.

Keywords

Dictyostelium; Erk activity; cAMP signaling; collective behavior; coupled oscillations; developmental time; oscillatory signaling; stochastic signaling; subcellular localization; transcription factors.

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