Thiaville Michelle M, Dudenhausen Elizabeth E, Zhong Can, Pan Yuan-Xiang, Kilberg Michael S
Department of Biochemistry and Molecular Biology, Center for Nutritional Sciences, and Shands Cancer Center, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Biochem J. 2008 Mar 15;410(3):473-84. doi: 10.1042/BJ20071252.
A nutrient stress signalling pathway is triggered in response to protein or amino acid deprivation, namely the AAR (amino acid response), and previous studies have shown that C/EBPbeta (CCAAT/enhancer-binding protein beta) expression is up-regulated following activation of the AAR. DNA-binding studies, both in vitro and in vivo, have revealed increased C/EBPbeta association with AARE (AAR element) sequences in AAR target genes, but its role is still unresolved. The present results show that in HepG2 human hepatoma cells, the total amount of C/EBPbeta protein, both the activating [LAP* and LAP (liver-enriched activating protein)] and inhibitory [LIP (liver-enriched inhibitory)] isoforms, was increased in histidine-deprived cells. Immunoblotting of subcellular fractions and immunostaining revealed that most of the C/EBPbeta was located in the nucleus. Consistent with these observations, amino acid limitation caused an increase in C/EBPbeta DNA-binding activity in nuclear extracts and chromatin immunoprecipitation revealed an increase in C/EBPbeta binding to the AARE region in vivo, but at a time when transcription from the target gene was declining. A constant fraction of the basal and increased C/EBPbeta protein was phosphorylated on Thr(235) and the phospho-C/EBPbeta did bind to an AARE. Induction of AARE-enhanced transcription was slightly greater in C/EBPbeta-deficient MEFs (mouse embryonic fibroblasts) or C/EBPbeta siRNA (small interfering RNA)-treated HepG2 cells compared with the corresponding control cells. Transient expression of LAP*, LAP or LIP in C/EBPbeta-deficient fibroblasts caused suppression of increased transcription from an AARE-driven reporter gene. Collectively, the results demonstrate that C/EBPbeta is not required for transcriptional activation by the AAR pathway but, when present, acts in concert with ATF3 (activating transcription factor 3) to suppress transcription during the latter stages of the response.
响应蛋白质或氨基酸缺乏会触发一种营养应激信号通路,即氨基酸应答(AAR),先前的研究表明,AAR激活后C/EBPβ(CCAAT/增强子结合蛋白β)的表达会上调。体外和体内的DNA结合研究均显示,AAR靶基因中与AARE(AAR元件)序列结合的C/EBPβ增加,但其作用仍未明确。目前的结果表明,在HepG2人肝癌细胞中,组氨酸缺乏的细胞中C/EBPβ蛋白的总量,包括激活型[LAP和LAP(肝脏富集激活蛋白)]和抑制型[LIP(肝脏富集抑制蛋白)]异构体,均增加。亚细胞组分的免疫印迹和免疫染色显示,大多数C/EBPβ位于细胞核中。与这些观察结果一致,氨基酸限制导致核提取物中C/EBPβ的DNA结合活性增加,染色质免疫沉淀显示体内C/EBPβ与AARE区域的结合增加,但此时靶基因的转录却在下降。基础和增加的C/EBPβ蛋白中有一定比例在Thr(235)位点被磷酸化,磷酸化的C/EBPβ确实能与AARE结合。与相应的对照细胞相比,在C/EBPβ缺陷的MEF(小鼠胚胎成纤维细胞)或C/EBPβ siRNA(小干扰RNA)处理的HepG2细胞中,AARE增强的转录诱导作用略强。在C/EBPβ缺陷的成纤维细胞中瞬时表达LAP、LAP或LIP会抑制AARE驱动的报告基因转录的增加。总体而言,结果表明C/EBPβ不是AAR途径转录激活所必需的,但当其存在时,会与ATF3(激活转录因子3)协同作用,在应答的后期阶段抑制转录。