Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/136224
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dc.creatorMoreira, S
dc.creatorOsswald, M
dc.creatorVentura, G
dc.creatorGonçalves, M
dc.creatorSunkel, CE
dc.creatorMorais-de-Sá, E
dc.date.accessioned2021-09-20T10:52:04Z-
dc.date.available2021-09-20T10:52:04Z-
dc.date.issued2019
dc.identifier.issn2211-1247
dc.identifier.urihttps://hdl.handle.net/10216/136224-
dc.description.abstractApical-basal polarity is a common trait that underlies epithelial function. Although the asymmetric distribution of cortical polarity proteins works in a functioning equilibrium, it also retains plasticity to accommodate cell division, during which the basolateral determinant Lgl is released from the cortex. Here, we investigated how Lgl restores its cortical localization to maintain the integrity of dividing epithelia. We show that cytoplasmic Lgl is reloaded to the cortex at mitotic exit in Drosophila epithelia. Lgl cortical localization depends on protein phosphatase 1, which dephosphorylates Lgl on the serines phosphorylated by aPKC and Aurora A kinases through a mechanism that relies on the regulatory subunit Sds22 and a PP1-interacting RVxF motif of Lgl. This mechanism maintains epithelial polarity and is of particular importance at mitotic exit to couple Lgl cortical reloading with the polarization of the apical domain. Hence, PP1-mediated dephosphorylation of Lgl preserves the apicalbasal organization of proliferative epithelia.
dc.description.sponsorshipWe thank Daniel St Johnston, François Schweisguth, Guilles Hickson, Jürgen Knoblich, Torcato Martins, Yang Hong, and the Bloomington Drosophila Stock Center for providing plasmids and fly stocks. This work was funded by national funds through Fundação para a Ciência e a Tecnologia (FCT) under project PTDC/BEX-BCM/0432/2014 . This work has also received funding from the project Norte-01-0145-FEDER-000029 , supported by Norte Portugal Regional Operational Program (NORTE 2020). E.M. holds an FCT Investigator position. S.M. and M.G. are supported by FCT PhD grants. M.O. is supported by a fellowship from FCT and the GABBA PhD program from the University of Porto .
dc.language.isoeng
dc.publisherCell Press
dc.relation.ispartofCell Reports, vol.26(2), p. 293-301.e7
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectaPKC
dc.subjectcell division
dc.subjectcell polarity
dc.subjectDrosophila
dc.subjectepithelial tissue
dc.subjectLgl
dc.subjectlive imaging
dc.subjectmitosis
dc.subjectphosphorylation
dc.subjectprotein phosphatase 1
dc.subject.meshAnimals
dc.subject.meshAurora Kinase A / metabolism
dc.subject.meshBinding Sites
dc.subject.meshCell Polarity
dc.subject.meshDrosophila Proteins / chemistry
dc.subject.meshDrosophila Proteins / genetics
dc.subject.meshDrosophila Proteins / metabolism
dc.subject.meshDrosophila melanogaster
dc.subject.meshEpithelial Cells / metabolism
dc.subject.meshMitosis
dc.subject.meshProtein Binding
dc.subject.meshProtein Phosphatase 1 / metabolism
dc.subject.meshProtein Transport
dc.subject.meshTumor Suppressor Proteins / chemistry
dc.subject.meshTumor Suppressor Proteins / genetics
dc.subject.meshTumor Suppressor Proteins / metabolism
dc.titlePP1-Mediated Dephosphorylation of Lgl Controls Apical-basal Polarity
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.1016/j.celrep.2018.12.060
dc.relation.publisherversionhttps://www.cell.com/cell-reports/fulltext/S2211-1247(18)32005-9?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS2211124718320059%3Fshowall%3Dtrue
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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