Transcriptomic profile of Pea3 family members reveal regulatory codes for axon outgrowth and neuronal connection specificity

dc.contributor.authorKandemir, Basak
dc.contributor.authorGulfidan, Gizem
dc.contributor.authorArga, Kazim Yalcin
dc.contributor.authorYilmaz, Bayram
dc.contributor.authorKurnaz, Isil Aksan
dc.date.accessioned2025-10-29T11:20:17Z
dc.date.issued2020
dc.departmentEnstitüler, Lisansüstü Eğitim Enstitüsü, Biyomühendislik Ana Bilim Dalı
dc.description.abstractPEA3 transcription factor subfamily is present in a variety of tissues with branching morphogenesis, and play a particularly significant role in neural circuit formation and specificity. Many target genes in axon guidance and cell-cell adhesion pathways have been identified for Pea3 transcription factor (but not for Erm or Er81); however it was not so far clear whether all Pea3 subfamily members regulate same target genes, or whether there are unique targets for each subfamily member that help explain the exclusivity and specificity of these proteins in neuronal circuit formation. In this study, using transcriptomics and qPCR analyses in SH-SY5Y neuroblastoma cells, hypothalamic and hippocampal cell line, we have identified cell type-specific and subfamily member-specific targets for PEA3 transcription factor subfamily. While Pea3 upregulates transcription of Sema3D and represses Sema5B, for example, Erm and Er81 upregulate Sema5A and Er81 regulates Unc5C and Sema4G while repressing EFNB3 in SH-SY5Y neuroblastoma cells. We furthermore present a molecular model of how unique sites within the ETS domain of each family member can help recognize specific target motifs. Such cell-context and member-specific combinatorial expression profiles help identify cell-cell and cell-extracellular matrix communication networks and how they establish specific connections.
dc.description.sponsorshipTUBITAK [214Z278]
dc.description.sponsorshipWe would like to acknowledge TUBITAK Grant no 214Z278. We would also like to acknowledge SEM company for their excellent assistance with microarray assay, and also give our special thanks to undergraduate project students Ekin Sonmez for help with qPCR analyses and promoter clonings. YOK 100/2000 PhD Scholarship to Gizem Gulfidan is acknowledged.
dc.identifier.doi10.1038/s41598-020-75089-3
dc.identifier.issn2045-2322
dc.identifier.issue1
dc.identifier.orcid0000-0003-1909-5778
dc.identifier.orcid0000-0002-2674-6535
dc.identifier.pmid33097800
dc.identifier.scopus2-s2.0-85093947431
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1038/s41598-020-75089-3
dc.identifier.urihttps://hdl.handle.net/20.500.14854/8524
dc.identifier.volume10
dc.identifier.wosWOS:000586489900004
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherNature Portfolio
dc.relation.ispartofScientific Reports
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20251020
dc.subjectMotor-Neurons
dc.subjectEts
dc.subjectEtv4
dc.subjectPathways
dc.subjectFgf8
dc.titleTranscriptomic profile of Pea3 family members reveal regulatory codes for axon outgrowth and neuronal connection specificity
dc.typeArticle

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