19
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Cdc42 defines apical identity and regulates epithelial morphogenesis by promoting apical recruitment of Par6-aPKC and Crumbs

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          ABSTRACT

          Cdc42 regulates epithelial morphogenesis together with the Par complex (Baz/Par3-Par6-aPKC), Crumbs (Crb/CRB3) and Stardust (Sdt/PALS1). However, how these proteins work together and interact during epithelial morphogenesis is not well understood. To address this issue, we used the genetically amenable Drosophila pupal photoreceptor and follicular epithelium. We show that during epithelial morphogenesis active Cdc42 accumulates at the developing apical membrane and cell-cell contacts, independently of the Par complex and Crb. However, membrane localization of Baz, Par6-aPKC and Crb all depend on Cdc42. We find that although binding of Cdc42 to Par6 is not essential for the recruitment of Par6 and aPKC to the membrane, it is required for their apical localization and accumulation, which we find also depends on Par6 retention by Crb. In the pupal photoreceptor, membrane recruitment of Par6-aPKC also depends on Baz. Our work shows that Cdc42 is required for this recruitment and suggests that this factor promotes the handover of Par6-aPKC from Baz onto Crb. Altogether, we propose that Cdc42 drives morphogenesis by conferring apical identity, Par-complex assembly and apical accumulation of Crb.

          Abstract

          Summary: During epithelia morphogenesis in Drosophila, the Rho-GTPase Cdc42 confers apical identity, Par-complex assembly and Crb accumulation to promote epithelial morphogenesis.

          Related collections

          Most cited references66

          • Record: found
          • Abstract: found
          • Article: not found

          Construction of transgenic Drosophila by using the site-specific integrase from phage phiC31.

          The phiC31 integrase functions efficiently in vitro and in Escherichia coli, yeast, and mammalian cells, mediating unidirectional site-specific recombination between its attB and attP recognition sites. Here we show that this site-specific integration system also functions efficiently in Drosophila melanogaster in cultured cells and in embryos. Intramolecular recombination in S2 cells on transfected plasmid DNA carrying the attB and attP recognition sites occurred at a frequency of 47%. In addition, several endogenous pseudo attP sites were identified in the fly genome that were recognized by the integrase and used as substrates for integration in S2 cells. Two lines of Drosophila were created by integrating an attP site into the genome with a P element. phiC31 integrase injected into embryos as mRNA functioned to promote integration of an attB-containing plasmid into the attP site, resulting in up to 55% of fertile adults producing transgenic offspring. A total of 100% of these progeny carried a precise integration event at the genomic attP site. These experiments demonstrate the potential for precise genetic engineering of the Drosophila genome with the phiC31 integrase system and will likely benefit research in Drosophila and other insects.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Analysis of genetic mosaics in developing and adult Drosophila tissues.

            T Xu, G Rubin (1993)
            We have constructed a series of strains to facilitate the generation and analysis of clones of genetically distinct cells in developing and adult tissues of Drosophila. Each of these strains carries an FRT element, the target for the yeast FLP recombinase, near the base of a major chromosome arm, as well as a gratuitous cell-autonomous marker. Novel markers that carry epitope tags and that are localized to either the cell nucleus or cell membrane have been generated. As a demonstration of how these strains can be used to study a particular gene, we have analyzed the developmental role of the Drosophila EGF receptor homolog. Moreover, we have shown that these strains can be utilized to identify new mutations in mosaic animals in an efficient and unbiased way, thereby providing an unprecedented opportunity to perform systematic genetic screens for mutations affecting many biological processes.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Genetic transformation of Drosophila with transposable element vectors.

              Exogenous DNA sequences were introduced into the Drosophila germ line. A rosy transposon (ry1), constructed by inserting a chromosomal DNA fragment containing the wild-type rosy gene into a P transposable element, transformed germ line cells in 20 to 50 percent of the injected rosy mutant embryos. Transformants contained one or two copies of chromosomally integrated, intact ry1 that were stably inherited in subsequent generations. These transformed flies had wild-type eye color indicating that the visible genetic defect in the host strain could be fully and permanently corrected by the transferred gene. To demonstrate the generality of this approach, a DNA segment that does not confer a recognizable phenotype on recipients was also transferred into germ line chromosomes.
                Bookmark

                Author and article information

                Journal
                Development
                Development
                DEV
                develop
                Development (Cambridge, England)
                The Company of Biologists Ltd
                0950-1991
                1477-9129
                1 August 2019
                12 August 2019
                12 August 2019
                : 146
                : 15
                : dev175497
                Affiliations
                [1 ]MRC - Laboratory for Molecular Cell Biology, University College London , London WC1E 6BT, UK
                [2 ]Institute for the Physics of Living Systems, University College London , London WC1E 6BT, UK
                Author notes
                [*]

                Present address: Department of Pharmacology, Irving Cancer Research Center, Columbia University Medical Center, 1130 St Nicholas Avenue, New York, NY 10032, USA.

                [‡]

                Co-first authors

                [§ ]Authors for correspondence ( r.walther@ 123456ucl.ac.uk ; f.pichaud@ 123456ucl.ac.uk )
                Author information
                http://orcid.org/0000-0002-6655-9806
                http://orcid.org/0000-0002-8393-716X
                Article
                DEV175497
                10.1242/dev.175497
                6703713
                31405903
                55ea6f4e-fc52-426b-9edc-65b30f012485
                © 2019. Published by The Company of Biologists Ltd

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 8 January 2019
                : 10 July 2019
                Funding
                Funded by: Medical Research Council;
                Award ID: MC_UU_12018/3
                Award ID: MC_UU_00012/3
                Categories
                Research Article

                Developmental biology
                epithelial polarity,cdc42,par6,par3,bazooka,apkc,crumbs,par complex
                Developmental biology
                epithelial polarity, cdc42, par6, par3, bazooka, apkc, crumbs, par complex

                Comments

                Comment on this article