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      An Instructive Role for C. elegans HMR-1/E-cadherin in Translating Cell Contact Cues into Cortical Polarity

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          Abstract

          Cell contacts provide spatial cues that polarize early embryos and epithelial cells. The homophilic adhesion protein E-cadherin is required for contact-induced polarity in many cells. However, it is debated whether E-cadherin functions instructively as a spatial cue, or permissively by ensuring adequate adhesion so that cells can sense other contact signals. In C. elegans, contacts polarize early embryonic cells by recruiting the RhoGAP PAC-1 to the adjacent cortex, inducing PAR protein asymmetry. Here we show that HMR-1/E-cadherin, which is dispensable for adhesion, functions together with HMP-1/α-catenin, JAC-1/p120 catenin, and the previously uncharacterized linker PICC-1/CCDC85/DIPA to bind PAC-1 and recruit it to contacts. Mislocalizing the HMR-1 intracellular domain to contact-free surfaces draws PAC-1 to these sites and depolarizes cells, demonstrating an instructive role for HMR-1 in polarization. Our findings identify an E-cadherin-mediated pathway that translates cell contacts into cortical polarity by directly recruiting a symmetry-breaking factor to the adjacent cortex.

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          Most cited references56

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          Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences.

          We describe a dominant behavioral marker, rol-6(su-1006), and an efficient microinjection procedure which facilitate the recovery of Caenorhabditis elegans transformants. We use these tools to study the mechanism of C.elegans DNA transformation. By injecting mixtures of genetically marked DNA molecules, we show that large extrachromosomal arrays assemble directly from the injected molecules and that homologous recombination drives array assembly. Appropriately placed double-strand breaks stimulated homologous recombination during array formation. Our data indicate that the size of the assembled transgenic structures determines whether or not they will be maintained extrachromosomally or lost. We show that low copy number extrachromosomal transformation can be achieved by adjusting the relative concentration of DNA molecules in the injection mixture. Integration of the injected DNA, though relatively rare, was reproducibly achieved when single-stranded oligonucleotide was co-injected with the double-stranded DNA.
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            Specific interference by ingested dsRNA.

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              Cell polarity in eggs and epithelia: parallels and diversity.

              Cell polarity, the generation of cellular asymmetries, is necessary for diverse processes in animal cells, such as cell migration, asymmetric cell division, epithelial barrier function, and morphogenesis. Common mechanisms generate and transduce cell polarity in different cells, but cell type-specific processes are equally important. In this review, we highlight the similarities and differences between the polarity mechanisms in eggs and epithelia. We also highlight the prospects for future studies on how cortical polarity interfaces with other cellular processes, such as morphogenesis, exocytosis, and lipid signaling, and how defects in polarity contribute to tumor formation. Copyright 2010 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                100890575
                21417
                Nat Cell Biol
                Nat. Cell Biol.
                Nature cell biology
                1465-7392
                1476-4679
                28 March 2015
                04 May 2015
                June 2015
                01 December 2015
                : 17
                : 6
                : 726-735
                Affiliations
                [1 ]Helen L. and Martin S. Kimmel Center for Biology and Medicine at the Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, NY 10016, USA
                [2 ]Department of Cell Biology, NYU School of Medicine, New York, NY 10016, USA
                Author notes
                [* ]Author for correspondence: Jeremy Nance, NYU School of Medicine, Skirball Institute of Biomolecular Medicine, 540 First Avenue, 4 th floor lab 17, New York, NY 10016, 212-263-3156 (office), 212-263-7760 (fax), Jeremy.Nance@ 123456med.nyu.edu
                Article
                NIHMS675683
                10.1038/ncb3168
                4449804
                25938815
                319a7560-5c1d-45bf-acab-43f8fd1bd526
                History
                Categories
                Article

                Cell biology
                polarity,cell contact,adhesion,e-cadherin,rhogap,par-6
                Cell biology
                polarity, cell contact, adhesion, e-cadherin, rhogap, par-6

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