Activating transcription factor 4 mediates up-regulation of alanine aminotransferase 2 gene expression under metabolic stress

被引:17
|
作者
Salgado, Maria C. [1 ]
Meton, Isidoro [1 ]
Anemaet, Ida G. [1 ]
Baanante, Isabel V. [1 ]
机构
[1] Univ Barcelona, Fac Farm, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2014年 / 1839卷 / 04期
关键词
Alanine aminotransferase 2; Alanine aminotransferase 1; Activating transcription factor 4; Amino acid deprivation; ER stress; Gene knock-down; ENDOPLASMIC-RETICULUM STRESS; TYPE-2; DIABETES-MELLITUS; AMINO-ACID DEPRIVATION; INSULIN-RESISTANCE; SPARUS-AURATA; TISSUE EXPRESSION; OXIDATIVE STRESS; LIVER-ENZYMES; SERUM; ATF4;
D O I
10.1016/j.bbagrm.2014.01.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alanine aminotransferase (ALT) provides a molecular link between carbohydrate and amino acid metabolism. In humans, two ALT isoforms have been characterized: ALT1, cytosolic, and ALT2, mitochondrial. To gain insight into the transcriptional regulation of the ALT2 gene, we cloned and characterized the human ALT2 promoter. 5'-deletion analysis of ALT2 promoter in transiently transfected HepG2 cells and site-directed mutagenesis allowed us to identify ATF4 as a new factor involved in the transcriptional regulation of ALT2 expression. Quantitative RT-PCR assays showed that the metabolic stressors histidinol and tunicamycin increased ATF4 levels and up-regulated ALT2 in HepG2 and Huh7 cells. Consistently, knockdown of ATF4 decreased ALT2 mRNA levels in HepG2 and Huh-7 cells. Moreover, ATF4 silencing prevented the activating effect of histidinol and tunicamycin on ATF4 and ALT2 expression. Our findings point to ALT2 as an enzyme involved in the metabolic adaptation of the cell to stress. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:288 / 296
页数:9
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