Premium
Expression of the glycine transporter type 1 (GlyT‐1A) is upregulated by ATF‐4 following physiological stress in human intestinal epithelial cells (1109.14)
Author(s) -
Fultang Livingstone,
Howard Alison,
Hirst Barry
Publication year - 2014
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.28.1_supplement.1109.14
Subject(s) - chromatin immunoprecipitation , reporter gene , microbiology and biotechnology , untranslated region , chemistry , promoter , exon , gene , tunicamycin , endoplasmic reticulum , gene expression , biology , unfolded protein response , biochemistry , messenger rna
Downstream of activating transcription factor 4 (ATF‐4) in Caco‐2 cells in response to stress. In the present study we show that increased expression of the GlyT‐1a gene following stress is dependent on elements contained within the 5’untranslated region (UTR). Caco‐2 cells transfected with plasmid constructs containing sequences representative of the GlyT‐1a proximal promoter and 5’UTR upstream of a beta‐galactosidase reporter showed increased reporter activity following treatment with thapsigargin (Tg), tunicamycin (Tu), amino acid (AA) starvation, tertbutylhydroquinone(tBHQ) or Diethyl maleate (DEM). Short labeled DNA probes containing a potential amino acid response element (AARE) located in exon 1 of the GLYT‐1a gene demonstrated binding by ATF‐4 in gel shift and super shift assays. qPCR assays performed on short genomic DNA fragments isolated from Caco‐2 cells by chromatin immunoprecipitation (ChIP) with antibodies against ATF4 demonstrated 9, 5 and 2‐fold enrichment of the ATF‐4/AARE interaction at the 5’‐UTR region of GlyT1a following Tu, AA starvation and DEM treatment respectively. Our data suggests that response elements within the 5’UTR including exon 1 and the first 85 bases of exon 2 are required for transcriptional induction of GlyT1a. We propose the direct interaction of ATF‐4 at the identified AARE drives transcriptional up‐regulation of GlyT‐1a following nutrient, oxidative and endoplasmic reticulum stress. Grant Funding Source : University of Newcastle