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dc.creatorRouka E., Gourgoulianni N., Lüpold S., Hatzoglou C., Gourgoulianis K., Blanckenhorn W.U., Zarogiannis S.G.en
dc.date.accessioned2023-01-31T09:51:51Z
dc.date.available2023-01-31T09:51:51Z
dc.date.issued2021
dc.identifier10.1111/apha.13527
dc.identifier.issn17481708
dc.identifier.urihttp://hdl.handle.net/11615/78562
dc.description.abstractThe involvement of Septate Junctions (SJs) in critical cellular functions that extend beyond their role as diffusion barriers in the epithelia and the nervous system has made the fruit fly an ideal model for the study of human diseases associated with impaired Tight Junction (TJ) function. In this study, we summarized current knowledge of the Drosophila melanogaster SJ-related proteins, focusing on their unconventional functions. Additionally, we sought to identify human orthologs of the corresponding genes as well as protein domain families. The systematic literature search was performed in PubMed and Scopus databases using relevant key terms. Orthologs were predicted using the DIOPT tool and aligned protein regions were determined from the Pfam database. 3-D models of the smooth SJ proteins were built on the Phyre2 and DMPFold protein structure prediction servers. A total of 30 proteins were identified as relatives to the SJ cellular structure. Key roles of these proteins, mainly in the regulation of morphogenetic events and cellular signalling, were highlighted. The investigation of protein domain families revealed that the SJ-related proteins contain conserved domains that are required not only for cell-cell interactions and cell polarity but also for cellular signalling and immunity. DIOPT analysis of orthologs identified novel human genes as putative functional homologs of the fruit fly SJ genes. A gap in our knowledge was identified regarding the domains that occur in the proteins encoded by eight SJ-associated genes. Future investigation of these domains is needed to provide functional information. © 2020 Scandinavian Physiological Society. Published by John Wiley & Sons Ltden
dc.language.isoenen
dc.sourceActa Physiologicaen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85089005164&doi=10.1111%2fapha.13527&partnerID=40&md5=f66467f9d7657f1a4311b946ccdfd0b1
dc.subjectDrosophila proteinen
dc.subjectmembrane proteinen
dc.subjectamino acid sequenceen
dc.subjectblood brain barrieren
dc.subjectcell interactionen
dc.subjectcell polarityen
dc.subjectdata baseen
dc.subjectDrosophila melanogasteren
dc.subjecthumanen
dc.subjectimmune responseen
dc.subjectintestine functionen
dc.subjectMalpighian tubuleen
dc.subjectmidguten
dc.subjectmorphogenesisen
dc.subjectnonhumanen
dc.subjectpriority journalen
dc.subjectprotein analysisen
dc.subjectprotein domainen
dc.subjectprotein familyen
dc.subjectprotein structureen
dc.subjectReviewen
dc.subjectsalivary glanden
dc.subjectseptate junctionen
dc.subjectsignal transductionen
dc.subjectanimalen
dc.subjectcell junctionen
dc.subjectDrosophilaen
dc.subjectDrosophila melanogasteren
dc.subjectgeneticsen
dc.subjecttight junctionen
dc.subjectAnimalsen
dc.subjectDrosophilaen
dc.subjectDrosophila melanogasteren
dc.subjectHumansen
dc.subjectIntercellular Junctionsen
dc.subjectMembrane Proteinsen
dc.subjectProtein Domainsen
dc.subjectTight Junctionsen
dc.subjectBlackwell Publishing Ltden
dc.titleThe Drosophila septate junctions beyond barrier function: Review of the literature, prediction of human orthologs of the SJ-related proteins and identification of protein domain familiesen
dc.typeotheren


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