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      GAS2-like proteins mediate communication between microtubules and actin through interactions with end-binding proteins

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          ABSTRACT

          Crosstalk between the microtubule (MT) and actin cytoskeletons is fundamental to many cellular processes including cell polarisation and cell motility. Previous work has shown that members of the growth-arrest-specific 2 (GAS2) family mediate the crosstalk between filamentous actin (F-actin) and MTs, but the molecular basis of this process remained unclear. By using fluorescence microscopy, we demonstrate that three members of this family, GAS2-like 1, GAS2-like 2 and GAS2-like 3 (G2L1, G2L2 and G2L3, also known as GAS2L1, GAS2L2 and GAS2L3, respectively) are differentially involved in mediating the crosstalk between F-actin and MTs. Although all localise to actin and MTs, only the exogenous expression of G2L1 and G2L2 influenced MT stability, dynamics and guidance along actin stress fibres. Biochemical analysis and live-cell imaging revealed that their functions are largely due to the association of these proteins with MT plus-end-binding proteins that bind to SxIP or SxLP motifs located at G2L C-termini. Our findings lead to a model in which end-binding (EB) proteins play a key role in mediating actin–MT crosstalk.

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          An EB1-binding motif acts as a microtubule tip localization signal.

          Microtubules are filamentous polymers essential for cell viability. Microtubule plus-end tracking proteins (+TIPs) associate with growing microtubule plus ends and control microtubule dynamics and interactions with different cellular structures during cell division, migration, and morphogenesis. EB1 and its homologs are highly conserved proteins that play an important role in the targeting of +TIPs to microtubule ends, but the underlying molecular mechanism remains elusive. By using live cell experiments and in vitro reconstitution assays, we demonstrate that a short polypeptide motif, Ser-x-Ile-Pro (SxIP), is used by numerous +TIPs, including the tumor suppressor APC, the transmembrane protein STIM1, and the kinesin MCAK, for localization to microtubule tips in an EB1-dependent manner. Structural and biochemical data reveal the molecular basis of the EB1-SxIP interaction and explain its negative regulation by phosphorylation. Our findings establish a general "microtubule tip localization signal" (MtLS) and delineate a unifying mechanism for this subcellular protein targeting process.
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            Genes specifically expressed at growth arrest of mammalian cells.

            A subtraction cDNA library enriched for RNA sequences preferentially expressed in growth-arrested cells was prepared. Six cDNA clones were identified, varying in abundance from 2% to 0.0002% of the library and in size from 0.8 to 10 kb. The corresponding mRNAs are downregulated with different kinetics upon induction of growth by serum. The kinetics of induction after serum starvation and density-dependent inhibition of two of these growth-arrest-specific (gas) genes were investigated in more detail. Two cell lines transformed by viral onc genes did not express the two gas genes. The full-length cDNA for one gene has been sequenced and the protein product preliminarily characterized by in vitro translation.
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              Spectroscopic determination of tryptophan and tyrosine in proteins.

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                Author and article information

                Journal
                J Cell Sci
                J. Cell. Sci
                joces
                jcs
                Journal of Cell Science
                The Company of Biologists (Bidder Building, 140 Cowley Road, Cambridge, CB4 0DL, UK )
                0021-9533
                1477-9137
                15 June 2014
                15 June 2014
                : 127
                : 12
                : 2672-2682
                Affiliations
                [1 ]Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester , Manchester M13 9PT, UK
                [2 ]Manchester Institute of Biotechnology, Faculty of Life Sciences , 131 Princess Street, Manchester M1 7DN, UK
                [3 ]Laboratory of Biomolecular Research, OFLC 106, Paul Scherrer Institut , 5232 Villigen PSI, Switzerland
                Author notes
                [*]

                Present address: Department of Medicine, University of California San Diego, 9500 Gilman Drive, La Jolla. CA 92093, USA.

                [‡]

                These authors contributed equally to this work

                [§ ]Author for correspondence ( christoph.ballestrem@ 123456manchester.ac.uk )
                Article
                10.1242/jcs.140558
                4058111
                24706950
                d46debe7-13d0-4d89-bbac-037782869ea9
                © 2014. Published by The Company of Biologists Ltd

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 12 August 2013
                : 12 March 2014
                Categories
                Research Article

                Cell biology
                gas2 family,gas2-like 1,gas2-like 2,gas2-like 3,end-binding protein,microtubule,actin,mt-tip localising signal,mtls

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