Postnatal Dynamics of Zeb2 Expression in Rat Brain: Analysis of Novel 3′ UTR Sequence Reveals a miR-9 Interacting Site

• Published in: Journal of molecular neuroscience 2014-01, Vol.52 (1), p.138-147
• Main Authors: Kropivšek, Klara, Pickford, Jasmine, Carter, David A.
• Format: Article
• Language: English
• Subjects: 3' Untranslated Regions; Animals; Biomedical and Life Sciences; Biomedicine; Brain; Brain - cytology; Brain - growth & development; Brain - metabolism; Cell Biology; Cells, Cultured; Cloning; DNA polymerase; Gene Expression Regulation, Developmental; Homeodomain Proteins - genetics; Homeodomain Proteins - metabolism; MicroRNAs; MicroRNAs - metabolism; Neurochemistry; Neurology; Neurons - metabolism; Neurosciences; Proteins; Proteomics; Rats; Rats, Sprague-Dawley; Repressor Proteins - genetics; Repressor Proteins - metabolism; RNA, Messenger - genetics; RNA, Messenger - metabolism; Transcription factors; Transcription, Genetic; Zinc Finger E-box Binding Homeobox 2
• ISSN: 0895-8696; 1559-1166
• DOI: 10.1007/s12031-013-0146-x

ZEB2 is a transcription factor with established roles in neurogenesis but no defined function in postnatal brain despite extensive neuronal expression in telencephalic structures. Multiple, incompletely annotated transcripts derive from the Zeb2 locus; the purpose of the present study was to structurally characterize rat brain Zeb2 transcripts with respect to 3′ untranslated (UTR) sequence in order to understand Zeb2 transcript regulation including possible interactions with regulatory molecules such as neuronal miRNAs. We cloned a 5054-nucleotide Zeb 2 3′ UTR that is included in the most abundant Zeb2 transcript in neonatal rat brain. Unique features of the distal 3′ UTR region included a number of brain-specific miRNA target sites; a highly conserved miR-9 target site at 3′ UTR position 4097 was selected for functional verification in transfection experiments. Parallel analysis of Zeb2 transcript, ZEB2 protein and miR-9 levels across postnatal brain cortical development revealed a significant accumulation of ZEB2 protein levels only between postnatal days P2 and P5 that was associated with an acute loss of postnatal miR-9 expression in cortex. These studies demonstrate novel features of Zeb2 gene expression in postnatal rat brain and highlight the importance of full transcript annotation for identifying the complement of potential transcript-interacting regulators.