Identification and characterization of the promoter and transcription factors regulating the expression of cerebral sodium/calcium exchanger 2 (NCX2) gene. (March 2022)

• Record Type: Journal Article
• Authors: Calabrese, Lucrezia; Serani, Angelo; Natale, Silvia; Tedeschi, Valentina; Guida, Natascia; Valsecchi, Valeria; Secondo, Agnese; Formisano, Luigi; Annunziato, Lucio; Molinaro, Pasquale
• Is Part Of: Cell calcium. Volume 102(2022)
• Publication Date: 2022-03
• Subjects: Promoter -- NCX2 -- Calcium homeostasis -- CREB1; Calcium -- Metabolism -- Periodicals; Vertebrates -- Physiology -- Periodicals; Calcium -- Physiological effect -- Periodicals; Cell physiology -- Periodicals; Calcium in the body -- Periodicals; 572.516
• DOI: 10.1016/j.ceca.2022.102542
• Languages: English
• ISSNs: 0143-4160

Abstract

Highlights: 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. Abstract: 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. Graphical abstract: Image, graphical abstract