Promoter demethylation of the asparagine synthetase gene is required for ATF4-dependent adaptation to asparagine depletion Journal Article


Authors: Jiang, J.; Srivastava, S.; Seim, G.; Pavlova, N. N.; King, B.; Zou, L.; Zhang, C.; Zhong, M.; Feng, H.; Kapur, R.; Wek, R. C.; Fan, J.; Zhang, J.
Article Title: Promoter demethylation of the asparagine synthetase gene is required for ATF4-dependent adaptation to asparagine depletion
Abstract: Tumor cells adapt to nutrient-limited environments by inducing gene expression that ensures adequate nutrients to sustain metabolic demands. For example, during amino acid limitations, ATF4 in the amino acid response induces expression of asparagine synthetase (ASNS), which provides for asparagine biosynthesis. Acute lymphoblastic leukemia (ALL) cells are sensitive to asparagine depletion, and administration of the asparagine depletion enzyme L-asparaginase is an important therapy option. ASNS expression can counterbalance L-asparaginase treatment by mitigating nutrient stress. Therefore, understanding the mechanisms regulating ASNS expression is important to define the adaptive processes underlying tumor progression and treatment. Here we show that DNA hypermethylation at the ASNS promoter prevents its transcriptional expression following asparagine depletion. Insufficient expression of ASNS leads to asparagine deficiency, which facilitates ATF4-independent induction of CCAAT-enhancer-binding protein homologous protein (CHOP), which triggers apoptosis. We conclude that chromatin accessibility is critical for ATF4 activity at the ASNS promoter, which can switch ALL cells from an ATF4-dependent adaptive response to ATF4-independent apoptosis during asparagine depletion. This work may also help explain why ALL cells are most sensitive to L-asparaginase treatment compared with other cancers. © 2019 Jiang et al. Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.
Keywords: proteins; cell death; gene expression; acute lymphoblastic leukemia; tumors; amino acids; biochemistry; diseases; dna hypermethylation; tumor progressions; nutrients; amino acid response; enhancer binding proteins; homologous proteins; metabolic demands; nutrient-limited environment
Journal Title: Journal of Biological Chemistry
Volume: 294
Issue: 49
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 2019-12-06
Start Page: 18674
End Page: 18684
Language: English
DOI: 10.1074/jbc.RA119.010447
PUBMED: 31659118
PROVIDER: scopus
PMCID: PMC6901317
DOI/URL:
Notes: Article -- Export Date: 2 January 2020 -- Source: Scopus
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  1. Natalya Nickolayevna Pavlova
    12 Pavlova
  2. Bryan Christopher King
    11 King