Amino Acid Deprivation Induces the Transcription Rate of the Human Asparagine Synthetase Gene through a Timed Program of Expression and Promoter Binding of Nutrient-responsive Basic Region/Leucine Zipper Transcription Factors as Well as Localized Histone Acetylation

• Published in: The Journal of biological chemistry 2004-12, Vol.279 (49), p.50829-50839
• Main Authors: Chen, Hong, Pan, Yuan-Xiang, Dudenhausen, Elizabeth E., Kilberg, Michael S.
• Format: Article
• Language: English
• Subjects: Acetylation; Activating Transcription Factor 3; Amino Acids - chemistry; Aspartate-Ammonia Ligase - biosynthesis; Aspartate-Ammonia Ligase - genetics; CCAAT-Enhancer-Binding Protein-beta - metabolism; Cell Line; Cell Line, Tumor; Chromatin - chemistry; Chromatin - metabolism; Chromatin Immunoprecipitation; Histones - chemistry; Histones - metabolism; Humans; Immunoblotting; Kinetics; Models, Biological; Plasmids - metabolism; Promoter Regions, Genetic; Protein Binding; Reverse Transcriptase Polymerase Chain Reaction; RNA - chemistry; RNA Polymerase II - chemistry; RNA, Messenger - metabolism; TATA-Box Binding Protein - chemistry; Time Factors; Trans-Activators - metabolism; Transcription Factor TFIIB - chemistry; Transcription, Genetic; Transfection
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M409173200

Expression of human asparagine synthetase (ASNS), which catalyzes asparagine and glutamate biosynthesis, is transcriptionally induced following amino acid deprivation. Previous overexpression and electrophoresis mobility shift analysis showed the involvement of the transcription factors ATF4, C/EBPβ, and ATF3-FL through the nutrient-sensing response element-1 (NSRE-1) within the ASNS promoter. Amino acid deprivation caused an elevated mRNA level for ATF4, C/EBPβ, and ATF3-FL, and the present study established that the nuclear protein content for ATF4 and ATF3-FL were increased during amino acid limitation, whereas C/EBPβ-LIP declined slightly. The total amount of C/EBPβ-LAP protein was unchanged, but changes in the distribution among multiple C/EBPβ-LAP forms were observed. Overexpression studies established that ATF4, ATF3-FL, and C/EBPβ-LAP could coordinately modulate the transcription from the human ASNS promoter. Chromatin immunoprecipitation demonstrated that amino acid deprivation increased ATF3-FL, ATF4, and C/EBPβ binding to the ASNS promoter and enhanced promoter association of RNA polymerase II, TATA-binding protein, and TFIIB of the general transcription machinery. A time course revealed a markedly different temporal order of interaction between these transcription factors and the ASNS promoter. During the initial 2 h, there was a 20-fold increase in ATF4 binding and a rapid increase in histone H3 and H4 acetylation, which closely paralleled the increased transcription rate of the ASNS gene, whereas the increase in ATF3-FL and C/EBPβ binding was considerably slower and more closely correlated with the decline in transcription rate between 2 and 6 h. The data suggest that ATF3-FL and C/EBPβ act as transcriptional suppressors for the ASNS gene to counterbalance the transcription rate activated by ATF4 following amino acid deprivation.