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      Coordination of Wing and Whole-Body Development at Developmental Milestones Ensures Robustness against Environmental and Physiological Perturbations

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          Abstract

          Development produces correctly patterned tissues under a wide range of conditions that alter the rate of development in the whole body. We propose two hypotheses through which tissue patterning could be coordinated with whole-body development to generate this robustness. Our first hypothesis states that tissue patterning is tightly coordinated with whole-body development over time. The second hypothesis is that tissue patterning aligns at developmental milestones. To distinguish between our two hypotheses, we developed a staging scheme for the wing imaginal discs of Drosophila larvae using the expression of canonical patterning genes, linking our scheme to three whole-body developmental events: moulting, larval wandering and pupariation. We used our scheme to explore how the progression of pattern changes when developmental time is altered either by changing temperature or by altering the timing of hormone synthesis that drives developmental progression. We found the expression pattern in the wing disc always aligned at moulting and pupariation, indicating that these key developmental events represent milestones. Between these milestones, the progression of pattern showed greater variability in response to changes in temperature and alterations in physiology. Furthermore, our data showed that discs from wandering larvae showed greater variability in patterning stage. Thus for wing disc patterning, wandering does not appear to be a developmental milestone. Our findings reveal that tissue patterning remains robust against environmental and physiological perturbations by aligning at developmental milestones. Furthermore, our work provides an important glimpse into how the development of individual tissues is coordinated with the body as a whole.

          Author Summary

          Between distantly related species, development converges at common morphological and genetic stages, called developmental milestones, to ensure the establishment of a basic body plan. Beyond these milestones greater variability in developmental processes builds species-specific form. We reasoned that developmental milestones might also act within a species to achieve robustness against environmental or physiological perturbation. To address this, we first developed a staging scheme for the progression of pattern in the wing disc across developmental time. We then explored how perturbing environmental or physiological stimuli known to alter the rate of development affected the progression of pattern in the wing disc. We found two developmental milestones, the moult to the third instar and pupariation, where wing disc patterning aligned with the development of the whole body. This suggests that robustness against environmental and physiological conditions is achieved by coordinating tissue with whole-body development at developmental milestones.

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          Most cited references24

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          Programmed autophagy in the Drosophila fat body is induced by ecdysone through regulation of the PI3K pathway.

          Eukaryotic cells catabolize their own cytoplasm by autophagy in response to amino acid starvation and inductive signals during programmed tissue remodeling and cell death. The Tor and PI3K signaling pathways have been shown to negatively control autophagy in eukaryotes, but the mechanisms that link these effectors to overall animal development and nutritional status in multicellular organisms remain poorly understood. Here, we reveal a complex regulation of programmed and starvation-induced autophagy in the Drosophila fat body. Gain-of-function genetic analysis indicated that ecdysone receptor signaling induces programmed autophagy whereas PI3K signaling represses programmed autophagy. Genetic interaction studies showed that ecdysone signaling downregulates PI3K signaling and that this represents the effector mechanism for induction of programmed autophagy. Hence, these studies link hormonal induction of autophagy to the regulatory function of the PI3K signaling pathway in vivo.
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            Senseless, a Zn finger transcription factor, is necessary and sufficient for sensory organ development in Drosophila.

            The senseless (sens) gene is required for proper development of most cell types of the embryonic and adult peripheral nervous system (PNS) of Drosophila. Sens is a nuclear protein with four Zn fingers that is expressed and required in the sensory organ precursors (SOP) for proper proneural gene expression. Ectopic expression of Sens in many ectodermal cells causes induction of PNS external sensory organ formation and is able to recreate an ectopic proneural field. Hence, sens is both necessary and sufficient for PNS development. Our data indicate that proneural genes activate sens expression. Sens is then in turn required to further activate and maintain proneural gene expression. This feedback mechanism is essential for selective enhancement and maintenance of proneural gene expression in the SOPs.
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              Patterning and growth control by membrane-tethered Wingless.

              Wnts are evolutionarily conserved secreted signalling proteins that, in various developmental contexts, spread from their site of synthesis to form a gradient and activate target-gene expression at a distance. However, the requirement for Wnts to spread has never been directly tested. Here we used genome engineering to replace the endogenous wingless gene, which encodes the main Drosophila Wnt, with one that expresses a membrane-tethered form of the protein. Surprisingly, the resulting flies were viable and produced normally patterned appendages of nearly the right size, albeit with a delay. We show that, in the prospective wing, prolonged wingless transcription followed by memory of earlier signalling allows persistent expression of relevant target genes. We suggest therefore that the spread of Wingless is dispensable for patterning and growth even though it probably contributes to increasing cell proliferation.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Genet
                PLoS Genet
                plos
                plosgen
                PLoS Genetics
                Public Library of Science (San Francisco, USA )
                1553-7390
                1553-7404
                June 2014
                19 June 2014
                : 10
                : 6
                : e1004408
                Affiliations
                [1 ]Development, Evolution and the Environment Laboratory, Instituto Gulbenkian de Ciência, Oeiras, Portugal
                [2 ]Dept. of Zoology, Michigan State University, East Lansing, Michigan, United States of America
                [3 ]Dept. of Biology, Lake Forest College, Lake Forest, Illinois, United States of America
                University of Lausanne, Switzerland
                Author notes

                The authors have declared that no competing interests exist.

                Conceived and designed the experiments: MMO AWS CKM. Performed the experiments: MMO. Analyzed the data: MMO AWS CKM. Contributed reagents/materials/analysis tools: AWS CKM. Wrote the paper: MMO AWS CKM.

                Article
                PGENETICS-D-14-00057
                10.1371/journal.pgen.1004408
                4063698
                24945255
                353b4f07-01aa-4d60-a859-55805ee95bec
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 7 January 2014
                : 14 April 2014
                Page count
                Pages: 16
                Funding
                MMO is supported by a doctoral fellowship from the Fundação para a Ciência e a Tecnologia (SFRH/BD/51181/2010) and by Fundação Calouste Gulbenkian. This work was funded by the Fundação Calouste Gulbenkian to CKM and by the National Science Foundation (IOS-0845847 and IOS-0919855) to AWS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Developmental Biology
                Morphogenesis
                Pattern Formation
                Organism Development
                Genetics
                Gene Expression
                Zoology
                Animal Physiology

                Genetics
                Genetics

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