| Literature DB >> 32268116 |
Robert T Williams1, Rohiverth Guarecuco1, Leah A Gates2, Douglas Barrows2, Maria C Passarelli3, Bryce Carey2, Lou Baudrier1, Swarna Jeewajee1, Konnor La1, Benjamin Prizer1, Sohail Malik4, Javier Garcia-Bermudez1, Xiphias Ge Zhu1, Jason Cantor5, Henrik Molina6, Thomas Carroll7, Robert G Roeder4, Omar Abdel-Wahab8, C David Allis2, Kıvanç Birsoy9.
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.Entities:
Keywords: ATF4; CRISPR; asparaginase; cancer metabolism; genetic screen; leukemia; transcription
Year: 2020 PMID: 32268116 PMCID: PMC7219601 DOI: 10.1016/j.cmet.2020.03.008
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287