In silico analyses and global transcriptional profiling reveal novel putative targets for Pea3 transcription factor related to its function in neurons

dc.contributor.authorKandemir, Basak
dc.contributor.authorDag, Ugur
dc.contributor.authorGungor, Burcu Bakir
dc.contributor.authorDurasi, Ilknur Melis
dc.contributor.authorErdogan, Burcu
dc.contributor.authorSahin, Eray
dc.contributor.authorSezerman, Ugur
dc.date.accessioned2025-10-29T11:12:25Z
dc.date.issued2017
dc.departmentEnstitüler, Lisansüstü Eğitim Enstitüsü, Biyomühendislik Ana Bilim Dalı
dc.description.abstractPea3 transcription factor belongs to the PEA3 subfamily within the ETS domain transcription factor superfamily, and has been largely studied in relation to its role in breast cancer metastasis. Nonetheless, Pea3 plays a role not only in breast tumor, but also in other tissues with branching morphogenesis, including kidneys, blood vasculature, bronchi and the developing nervous system. Identification of Pea3 target promoters in these systems are important for a thorough understanding of how Pea3 functions. Present study particularly focuses on the identification of novel neuronal targets of Pea3 in a combinatorial approach, through curation, computational analysis and microarray studies in a neuronal model system, SH-SY5Y neuroblastoma cells. We not only show that quite a number of genes in cancer, immune system and cell cycle pathways, among many others, are either up- or down-regulated by Pea3, but also identify novel targets including ephrins and ephrin receptors, semaphorins, cell adhesion molecules, as well as metalloproteases such as kallikreins, to be among potential target promoters in neuronal systems. Our overall results indicate that rather than early stages of neurite extension and axonal guidance, Pea3 is more involved in target identification and synaptic maturation.
dc.description.sponsorshipTUBITAK BIDEB
dc.description.sponsorshipTUBITAK [107S064, 214Z278]
dc.description.sponsorshipSupport was provided by TUBITAK BIDEB project grants to UD and BE; TUBITAK grants no 107S064 and 214Z278 to IK. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
dc.identifier.doi10.1371/journal.pone.0170585
dc.identifier.issn1932-6203
dc.identifier.issue2
dc.identifier.orcid0000-0003-1909-5778
dc.identifier.orcid0000-0002-5324-6472
dc.identifier.orcid0000-0002-2272-6270
dc.identifier.orcid0000-0003-0905-6783
dc.identifier.orcid0000-0002-0873-2439
dc.identifier.pmid28158215
dc.identifier.scopus2-s2.0-85011561356
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0170585
dc.identifier.urihttps://hdl.handle.net/20.500.14854/6267
dc.identifier.volume12
dc.identifier.wosWOS:000396161700015
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherPublic Library Science
dc.relation.ispartofPlos One
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20251020
dc.subjectHippocampal-Neurons
dc.subjectNeurite Outgrowth
dc.subjectKinase Activation
dc.subjectPrecursor Cells
dc.subjectMotor-Neurons
dc.subjectEph Receptors
dc.subjectC-Jun
dc.subjectEts
dc.subjectExpression
dc.subjectProtein
dc.titleIn silico analyses and global transcriptional profiling reveal novel putative targets for Pea3 transcription factor related to its function in neurons
dc.typeArticle

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