Abstract

It has been suggested that Staufen (Stau) is key in controlling the variability of the posterior boundary of the Hb anterior domain (xHb). However, its underlying mechanism is elusive. Here, we quantified the dynamic 3D expression of segmentation genes in Drosophila embryos. With improved control of measurement errors, we show xHb of stau- mutants reproducibly moves posteriorly by 10% of the embryo length (EL) to the wild type (WT) position in the nuclear cycle (nc) 14, and its variability at short time windows is comparable as that of the WT. Moreover, for stau- mutants, the upstream Bicoid (Bcd) gradients show equivalent relative intensity noise to that of the WT in nc12-nc14, and the downstream Even-skipped (Eve) and cephalic furrow (CF) show the same positional errors as the WT. Our results indicate that threshold-dependent activation and self-organized filtering are not mutually exclusive but could both be implemented in early Drosophila embryogenesis.

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All data generated or analysed during this study are included in the manuscript and supporting files.

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Author details

  1. Zhe Yang

    Center for Quantitative Biology, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  2. Hongcun Zhu

    Center for Quantitative Biology, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  3. Kakit Kong

    School of Physics, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  4. Xiaoxuan Wu

    Center for Quantitative Biology, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  5. Jiayi Chen

    Center for Quantitative Biology, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  6. Peiyao Li

    Center for Quantitative Biology, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  7. Jialong Jiang

    Center for Quantitative Biology, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  8. Jinchao Zhao

    School of Physics, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  9. Bofei Cui

    State Key Laboratory of Nuclear Physics and Technology & Center for Quantitative Biology, Peking University, Beijing, China
    Competing interests
    The authors declare that no competing interests exist.
  10. Feng Liu

    School of Physics, Peking University, Beijing, China
    For correspondence
    liufeng-phy@pku.edu.cn
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-9724-6127

Funding

National Natural Science Foundation of China (The General Program 31670852)

  • Feng Liu

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Copyright

© 2020, Yang et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

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  1. Zhe Yang
  2. Hongcun Zhu
  3. Kakit Kong
  4. Xiaoxuan Wu
  5. Jiayi Chen
  6. Peiyao Li
  7. Jialong Jiang
  8. Jinchao Zhao
  9. Bofei Cui
  10. Feng Liu
(2020)
The dynamic transmission of positional information in stau-mutants during Drosophila embryogenesis
eLife 9:e54276.
https://doi.org/10.7554/eLife.54276

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https://doi.org/10.7554/eLife.54276