Transcriptional Regulation Factors of the Human Mitochondrial Aspartate/Glutamate Carrier Gene, Isoform 2 (SLC25A13): USF1 as Basal Factor and FOXA2 as Activator in Liver Cells.
Paolo ConvertiniSimona TodiscoFrancesco De SantisIlaria PappalardoDominga IacobazziMaria Antonietta Castiglione MorelliYvonne N Fondufe-MittendorfGiuseppe MartelliFerdinando PalmieriVittoria InfantinoPublished in: International journal of molecular sciences (2019)
Mitochondrial carriers catalyse the translocation of numerous metabolites across the inner mitochondrial membrane, playing a key role in different cell functions. For this reason, mitochondrial carrier gene expression needs tight regulation. The human SLC25A13 gene, encoding for the mitochondrial aspartate/glutamate carrier isoform 2 (AGC2), catalyses the electrogenic exchange of aspartate for glutamate plus a proton, thus taking part in many metabolic processes including the malate-aspartate shuttle. By the luciferase (LUC) activity of promoter deletion constructs we identified the putative promoter region, comprising the proximal promoter (-442 bp/-19 bp), as well as an enhancer region (-968 bp/-768 bp). Furthermore, with different approaches, such as in silico promoter analysis, gene silencing and chromatin immunoprecipitation, we identified two transcription factors responsible for SLC25A13 transcriptional regulation: FOXA2 and USF1. USF1 acts as a positive transcription factor which binds to the basal promoter thus ensuring SLC25A13 gene expression in a wide range of tissues. The role of FOXA2 is different, working as an activator in hepatic cells. As a tumour suppressor, FOXA2 could be responsible for SLC25A13 high expression levels in liver and its downregulation in hepatocellular carcinoma (HCC).
Keyphrases
- transcription factor
- gene expression
- dna methylation
- oxidative stress
- genome wide identification
- induced apoptosis
- genome wide
- endothelial cells
- dna binding
- copy number
- cell cycle arrest
- poor prognosis
- nuclear factor
- endoplasmic reticulum stress
- induced pluripotent stem cells
- ms ms
- mesenchymal stem cells
- blood brain barrier
- dna damage
- signaling pathway
- cell therapy
- long non coding rna
- toll like receptor