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      Wingless Directly Represses DPP Morphogen Expression via an Armadillo/TCF/Brinker Complex

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          Abstract

          Background

          Spatially restricted morphogen expression drives many patterning and regeneration processes, but how is the pattern of morphogen expression established and maintained? Patterning of Drosophila leg imaginal discs requires expression of the DPP morphogen dorsally and the wingless (WG) morphogen ventrally. We have shown that these mutually exclusive patterns of expression are controlled by a self-organizing system of feedback loops that involve WG and DPP, but whether the feedback is direct or indirect is not known.

          Methods/Findings

          By analyzing expression patterns of regulatory DNA driving reporter genes in different genetic backgrounds, we identify a key component of this system by showing that WG directly represses transcription of the dpp gene in the ventral leg disc. Repression of dpp requires a tri-partite complex of the WG mediators armadillo (ARM) and dTCF, and the co-repressor Brinker, (BRK), wherein ARM•dTCF and BRK bind to independent sites within the dpp locus.

          Conclusions/Significance

          Many examples of dTCF repression in the absence of WNT signaling have been described, but few examples of signal-driven repression requiring both ARM and dTCF binding have been reported. Thus, our findings represent a new mode of WG mediated repression and demonstrate that direct regulation between morphogen signaling pathways can contribute to a robust self-organizing system capable of dynamically maintaining territories of morphogen expression.

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          Most cited references58

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          Wnt signaling: a common theme in animal development.

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            Stem cells and their niches.

            A constellation of intrinsic and extrinsic cellular mechanisms regulates the balance of self-renewal and differentiation in all stem cells. Stem cells, their progeny, and elements of their microenvironment make up an anatomical structure that coordinates normal homeostatic production of functional mature cells. Here we discuss the stem cell niche concept, highlight recent progress, and identify important unanswered questions. We focus on three mammalian stem cell systems where large numbers of mature cells must be continuously produced throughout adult life: intestinal epithelium, epidermal structures, and bone marrow.
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              Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF.

              The vertebrate transcription factors TCF (T cell factor) and LEF (lymphocyte enhancer binding factor) interact with beta-catenin and are hypothesized to mediate Wingless/Wnt signaling. We have cloned a maternally expressed Drosophila TCF family member, dTCF. dTCF binds a canonical TCF DNA motif and interacts with the beta-catenin homolog Armadillo. Previous studies have identified two regions in Armadillo required for Wingless signaling. One of these interacts with dTCF, while the other constitutes a transactivation domain. Mutations in dTCF and expression of a dominant-negative dTCF transgene cause a segment polarity phenotype and affect expression of the Wingless target genes engrailed and Ultrabithorax. Epistasis analysis positions dTCF downstream of armadillo. The Armadillo-dTCF complex mediates Wingless signaling as a bipartite transcription factor.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS ONE
                plos
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2007
                3 January 2007
                : 2
                : 1
                : e142
                Affiliations
                [1 ]Department of Developmental and Cell Biology, University of California Irvine, Irvine, California, United States of America
                [2 ]Department of Mathematics, University of California Irvine, Irvine, California, United States of America
                [3 ]Department of Microbiology and Molecular Genetics, University of California Irvine, Irvine, California, United States of America
                [4 ]Developmental Biology Center, University of California Irvine, Irvine, California, United States of America
                Max Planck Institute of Molecular Cell Biology and Genetics, Germany
                Author notes
                * To whom correspondence should be addressed. E-mail: jlmarsh@ 123456uci.edu

                Conceived and designed the experiments: JM TL HT AS MW. Performed the experiments: FW QN TL JP HT AS BN GS DI KG MW. Analyzed the data: JM FW QN TL JP HT AS BN GS DI KG MW. Wrote the paper: JM FW QN TL HT AS BN GS DI MW. Other: Designed and analyzed the computational model: FW QN DI GS BN.

                [¤a]

                Current address: Computer Science Department, University of Missouri-Columbia, Columbia, Missouri, United States of America

                [¤b]

                Current address: Department of Mathematics and Statistics, Dalhousie University, Halifax, Nova Scotia, Canada

                [¤c]

                Current address: Stowers Institute, Kansas City, Missouri, United States of America

                Article
                06-PONE-RA-00168R1
                10.1371/journal.pone.0000142
                1764032
                17206277
                ebdbd8d1-d74d-4c48-9492-7b13cb988309
                Theisen et al. 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
                : 29 September 2006
                : 8 December 2006
                Page count
                Pages: 10
                Categories
                Research Article
                Cell Biology
                Developmental Biology
                Genetics and Genomics/Gene Therapy

                Uncategorized
                Uncategorized

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