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

dc.contributor.author Kandemir, Basak
dc.contributor.author Dag, Ugur
dc.contributor.author Bakir Gungor, Burcu
dc.contributor.author Durasi, Ilknur Melis
dc.contributor.author Erdogan, Burcu
dc.contributor.author Sahin, Eray
dc.contributor.author Sezerman, Ugur
dc.contributor.author Kurnaz Aksan, Isil
dc.contributor.department AGÜ, Mühendislik Fakültesi, Bilgisayar Mühendisliği Bölümü en_US
dc.contributor.institutionauthor
dc.date.accessioned 2019-07-05T09:54:38Z
dc.date.available 2019-07-05T09:54:38Z
dc.date.issued 2017 en_US
dc.description Support 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. en_US
dc.description.abstract Pea3 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. en_US
dc.description.sponsorship TUBITAK BIDEB TUBITAK -107S064 / 214Z278 en_US
dc.identifier.citation PLOS ONE Volume: 12 Issue: 2 Article Number: e0170585 DOI: 10.1371/journal.pone.0170585 en_US
dc.identifier.issn 1932-6203
dc.identifier.other PubMed ID: 28158215
dc.identifier.other Accession Number: WOS:000396161700015
dc.identifier.other DOI: 10.1371/journal.pone.0170585
dc.identifier.other Article Number: e0170585
dc.identifier.uri http://acikerisim.agu.edu.tr/xmlui/handle/20.500.12573/70
dc.language.iso eng en_US
dc.publisher PUBLIC LIBRARY SCIENCE, 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA en_US
dc.relation.ispartofseries PLOS ONE;Volume: 12 Issue: 2
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject HIPPOCAMPAL-NEURONS en_US
dc.subject NEURITE OUTGROWTH en_US
dc.subject KINASE ACTIVATION en_US
dc.subject KINASE ACTIVATION en_US
dc.subject MOTOR-NEURONS en_US
dc.subject EPH RECEPTORS en_US
dc.subject C-JUN en_US
dc.subject ETS en_US
dc.subject EXPRESSION en_US
dc.subject PROTEIN en_US
dc.title In silico analyses and global transcriptional profiling reveal novel putative targets for Pea3 transcription factor related to its function in neurons en_US
dc.type article en_US

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