Identification and characterization of the promoter and transcription factors regulating the expression of cerebral sodium/calcium exchanger 2 (NCX2) gene

生物 转录因子 基因亚型 发起人 基因表达 细胞生物学 基因 遗传学
作者
Lucrezia Calabrese,Angelo Serani,Silvia Natale,Valentina Tedeschi,Natascia Guida,Valeria Valsecchi,Agnese Secondo,Luigi Formisano,Lucio Annunziato,Pasquale Molinaro
出处
期刊:Cell Calcium [Elsevier]
卷期号:102: 102542-102542 被引量:5
标识
DOI:10.1016/j.ceca.2022.102542
摘要

• NCX2 promoter is up-regulated by CREB1, Sp1 and Sp4 in PC12 cells. • NCX2 promoter has many putative binding sites for TFs involved in neuronal development and plasticity, regulation of processes related to metabolism, cell proliferation and oncogenesis. The isoform 2 of sodium-calcium exchanger family (NCX2) is selectively expressed in neuronal and glial cells where it participates in Ca 2+ -clearance following neuronal depolarization, synaptic plasticity, hippocampal-dependent learning and memory consolidation processes. On the other hand, NCX2 is also involved in a neuroprotective effect following stroke. Despite the relevance of this antiporter under physiological and pathophysiological conditions, no studies have been reported on its genetic/epigenetic regulation. Therefore, we identified, cloned, and characterized a transcriptional regulatory region (R3) of rat Slc8a2 gene encoding for NCX2. In particular, R3 sequence displayed a promoter activity in PC12, SH-SY5Y and U87MG cell lines consistent with their endogenous NCX2 expression levels. On the other hand, R3 failed to induce detectable luciferase activity in BHK cell line that does not express NCX2 under control conditions. These data support the hypothesis that R3 represents the promoter region of NCX2. Moreover, among several conserved binding sequences for transcription factors identified by in-silico analysis, we evaluated the transcriptional regulation and the binding sites of Sp1, Sp4, NFkB1, GATA2 and CREB1 on R3 sequence by using site-direct mutagenesis and ChIP assays. In particular, transfection of Sp1, Sp4, and CREB1 enhanced both R3 promoter activity and NCX2 transcription in PC12 cell line. More important, CREB1 transfection also enhanced NCX2 protein levels and NCX reverse mode activity in PC12 cells. Altogether, these data suggested that: (i) the identified region contained the regulatory promoter of the antiporter; (ii) NCX2 might represent a downstream effector of transcription factors involved in synaptic plasticity and neuronal survival.
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