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dc.contributor.authorGlittenberg, M.en
dc.contributor.authorPitsouli, Chrysoulaen
dc.contributor.authorGarvey, C.en
dc.contributor.authorDelidakis, Christosen
dc.contributor.authorBray, S.en
dc.creatorGlittenberg, M.en
dc.creatorPitsouli, Chrysoulaen
dc.creatorGarvey, C.en
dc.creatorDelidakis, Christosen
dc.creatorBray, S.en
dc.date.accessioned2019-11-04T12:50:39Z
dc.date.available2019-11-04T12:50:39Z
dc.date.issued2006
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53108
dc.description.abstractNotch is the receptor in a signalling pathway that operates in a diverse spectrum of developmental processes. Its ligands (e.g. Serrate) are transmembrane proteins whose signalling competence is regulated by the endocytosis-promoting E3 ubiquitin ligases, Mindbomb1 and Neuralized. The ligands also inhibit Notch present in the same cell (cis-inhibition). Here, we identify two conserved motifs in the intracellular domain of Serrate that are required for efficient endocytosis. The first, a dileucine motif, is dispensable for trans-activation and cis-inhibition despite the endocytic defect, demonstrating that signalling can be separated from bulk endocytosis. The second, a novel motif, is necessary for interactions with Mindbomb1/Neuralized and is strictly required for Serrate to trans-activate and internalise efficiently but not for it to inhibit Notch signalling. Cis-inhibition is compromised when an ER retention signal is added to Serrate, or when the levels of Neuralized are increased, and together these data indicate that cis-inhibitory interactions occur at the cell surface. The balance of ubiquitinated/unubiquitinated ligand will thus affect the signalling capacity of the cell at several levels. © 2006 European Molecular Biology Organization | All Rights Reserved.en
dc.sourceEMBO Journalen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-33750202549&doi=10.1038%2fsj.emboj.7601337&partnerID=40&md5=5d7d24181d755de4642e7c7398c5c206
dc.subjectarticleen
dc.subjectcontrolled studyen
dc.subjectpriority journalen
dc.subjectunclassified drugen
dc.subjectnonhumanen
dc.subjectsignal transductionen
dc.subjectAnimalsen
dc.subjectCalcium-Binding Proteinsen
dc.subjectIntercellular Signaling Peptides and Proteinsen
dc.subjectJagged1en
dc.subjectMembrane Proteinsen
dc.subjectNotchen
dc.subjectmembrane proteinen
dc.subjectnucleotide sequenceen
dc.subjectprotein motifen
dc.subjectCell Membraneen
dc.subjectDrosophila melanogasteren
dc.subjectprotein domainen
dc.subjectprotein protein interactionen
dc.subjectProtein Bindingen
dc.subjectDrosophilaen
dc.subjectDrosophila Proteinsen
dc.subjectProtein Structure, Tertiaryen
dc.subjectProtein Processing, Post-Translationalen
dc.subjecttransactivationen
dc.subjectAmino Acid Motifsen
dc.subjectcis isomeren
dc.subjectEndocytosisen
dc.subjectEndoplasmic Reticulumen
dc.subjectMindbomb1 proteinen
dc.subjectNeuralized proteinen
dc.subjectReceptor, Notch1en
dc.subjectSerrateen
dc.subjectTrans-Activation (Genetics)en
dc.subjectTranscriptional Activationen
dc.subjectUbiquitinen
dc.subjectUbiquitin-Protein Ligasesen
dc.subjectUbiquitinationen
dc.titleRole of conserved intracellular motifs in Serrate signalling, cis-inhibition and endocytosisen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1038/sj.emboj.7601337
dc.description.volume25
dc.description.startingpage4697
dc.description.endingpage4706
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :79</p>en
dc.source.abbreviationEMBO J.en
dc.contributor.orcidPitsouli, Chrysoula [0000-0003-4074-9684]
dc.gnosis.orcid0000-0003-4074-9684


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