ZBTB1 Regulates Asparagine Synthesis and Leukemia Cell Response to L-Asparaginase.

TitleZBTB1 Regulates Asparagine Synthesis and Leukemia Cell Response to L-Asparaginase.
Publication TypeJournal Article
Year of Publication2020
AuthorsWilliams RT, Guarecuco R, Gates LA, Barrows D, Passarelli MC, Carey B, Baudrier L, Jeewajee S, La K, Prizer B, Malik S, Garcia-Bermudez J, Zhu XGe, Cantor J, Molina H, Carroll T, Roeder RG, Abdel-Wahab O, C Allis D, Birsoy K
JournalCell Metab
Volume31
Issue4
Pagination852-861.e6
Date Published2020 Apr 07
ISSN1932-7420
Abstract

Activating transcription factor 4 (ATF4) is a master transcriptional regulator of the integrated stress response (ISR) that enables cell survival under nutrient stress. The mechanisms by which ATF4 couples metabolic stresses to specific transcriptional outputs remain unknown. Using functional genomics, we identified transcription factors that regulate the responses to distinct amino acid deprivation conditions. While ATF4 is universally required under amino acid starvation, our screens yielded a transcription factor, Zinc Finger and BTB domain-containing protein 1 (ZBTB1), as uniquely essential under asparagine deprivation. ZBTB1 knockout cells are unable to synthesize asparagine due to reduced expression of asparagine synthetase (ASNS), the enzyme responsible for asparagine synthesis. Mechanistically, ZBTB1 binds to the ASNS promoter and promotes ASNS transcription. Finally, loss of ZBTB1 sensitizes therapy-resistant T cell leukemia cells to L-asparaginase, a chemotherapeutic that depletes serum asparagine. Our work reveals a critical regulator of the nutrient stress response that may be of therapeutic value.

DOI10.1016/j.cmet.2020.03.008
Alternate JournalCell Metab.
PubMed ID32268116
PubMed Central IDPMC7219601
Grant ListR01 CA178765 / CA / NCI NIH HHS / United States
F30 CA247199 / CA / NCI NIH HHS / United States
R01 CA163086 / CA / NCI NIH HHS / United States
DP2 CA228042 / CA / NCI NIH HHS / United States
T32 GM007739 / GM / NIGMS NIH HHS / United States
F30 CA247026 / CA / NCI NIH HHS / United States

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