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Glutamine stimulates the gene expression and processing of sterol regulatory element binding proteins, thereby increasing the expression of their target genes
Author(s) -
Inoue Jun,
Ito Yuka,
Shimada Satoko,
Satoh Shinich,
Sasaki Takashi,
Hashidume Tsutomu,
Kamoshida Yuki,
Shimizu Makoto,
Sato Ryuichiro
Publication year - 2011
Publication title -
the febs journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 204
eISSN - 1742-4658
pISSN - 1742-464X
DOI - 10.1111/j.1742-4658.2011.08204.x
Subject(s) - sterol regulatory element binding protein , gene expression , gene , sterol , regulation of gene expression , microbiology and biotechnology , biology , expression (computer science) , regulatory sequence , glutamine , genetics , biochemistry , amino acid , cholesterol , computer science , programming language
Here we show that the larger the amount of glutamine added to the medium, the more the expression of genes related to lipid homeostasis is promoted by the activation of sterol regulatory element binding proteins (SREBPs) at the transcriptional and post‐translational levels in human hepatoma HepG2 cells. Glutamine increases the mRNA levels of several SREBP targets, including SREBP‐2. The gene expression of SREBP‐1a, a predominant form of SREBP‐1 in most cultured cells and a target of the general transcription factor Sp1, is significantly augmented by glutamine via an increased binding of Sp1 to the SREBP‐1a promoter. In contrast, the increased expression of SREBP targets including SREBP‐2 is due to stimulation of the processing of SREBP proteins by glutamine. It is also shown that glutamine accelerates SREBP processing through increased transport of the SREBP/SREBP cleavage‐activating protein complex from the endoplasmic reticulum to the Golgi apparatus. The processing of activating transcription factor 6 is activated by the same proteases as SREBPs in the Golgi in response to endoplasmic reticulum stress and is not induced by glutamine. Taken together, these results clearly demonstrate that glutamine brings about not only the induction of SREBP‐1a transcription but also the stimulation of SREBP processing, thereby facilitating the gene expression of SREBP targets in cultured cells.