PUBLICATION

Intercellular Coupling Regulates the Period of the Segmentation Clock

Authors
Herrgen, L., Ares, S., Morelli, L.G., Schröter, C., Jülicher, F., and Oates, A.C.
ID
ZDB-PUB-100726-2
Date
2010
Source
Current biology : CB   20(14): 1244-1253 (Journal)
Registered Authors
Herrgen, Leah, Oates, Andrew
Keywords
DEVBIO
MeSH Terms
  • Animals
  • Biological Clocks/physiology*
  • Body Patterning/physiology*
  • Computer Simulation
  • Gene Expression Regulation, Developmental/physiology*
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins/metabolism
  • Microscopy, Fluorescence
  • Models, Biological*
  • Receptors, Notch/metabolism
  • Signal Transduction/physiology*
  • Somites/physiology*
  • Time Factors
  • Zebrafish/embryology*
(all 14)
PubMed
20637620 Full text @ Curr. Biol.
Abstract
BACKGROUND: Coupled biological oscillators can tick with the same period. How this collective period is established is a key question in understanding biological clocks. We explore this question in the segmentation clock, a population of coupled cellular oscillators in the vertebrate embryo that sets the rhythm of somitogenesis, the morphological segmentation of the body axis. The oscillating cells of the zebrafish segmentation clock are thought to possess noisy autonomous periods, which are synchronized by intercellular coupling through the Delta-Notch pathway. Here we ask whether Delta-Notch coupling additionally influences the collective period of the segmentation clock. RESULTS: Using multiple-embryo time-lapse microscopy, we show that disruption of Delta-Notch intercellular coupling increases the period of zebrafish somitogenesis. Embryonic segment length and the spatial wavelength of oscillating gene expression also increase correspondingly, indicating an increase in the segmentation clock's period. Using a theory based on phase oscillators in which the collective period self-organizes because of time delays in coupling, we estimate the cell-autonomous period, the coupling strength, and the coupling delay from our data. Further supporting the role of coupling delays in the clock, we predict and experimentally confirm an instability resulting from decreased coupling delay time. CONCLUSIONS: Synchronization of cells by Delta-Notch coupling regulates the collective period of the segmentation clock. Our identification of the first segmentation clock period mutants is a critical step toward a molecular understanding of temporal control in this system. We propose that collective control of period via delayed coupling may be a general feature of biological clocks.
Genes / Markers
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Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
ta52b
    Point Mutation
    ti282a
      Point Mutation
      tm13
        Point Mutation
        tm98
          Point Mutation
          tp37
            Point Mutation
            tr233
              Point Mutation
              u11
                Point Mutation
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                Human Disease / Model
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                Sequence Targeting Reagents
                Fish
                Antibodies
                Orthology
                Engineered Foreign Genes
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                Mapping