天冬酰胺酶
ATF4
综合应力响应
转录因子
天冬酰胺
白血病
调节器
癌症研究
未折叠蛋白反应
转录调控
天冬酰胺合成酶
抄写(语言学)
氨基酸
细胞生物学
生物
生物化学
淋巴细胞白血病
遗传学
基因
信使核糖核酸
哲学
翻译(生物学)
语言学
作者
Christina Williamson,Rohiverth Guarecuco,Leah Gates,Douglas Barrows,Maria C. Passarelli,Bryce W. Carey,Lou Baudrier,Swarna K. A. Jeewajee,Konnor La,Benjamin Prizer,Sohail Malik,Javier García‐Bermúdez,Xiphias Ge Zhu,Jason R. Cantor,Henrik Molina,Thomas Carroll,Robert G. Roeder,Omar Abdel‐Wahab,C. David Allis,Kıvanç Birsoy
出处
期刊:Cell Metabolism
[Elsevier]
日期:2020-04-01
卷期号:31 (4): 852-861.e6
被引量:44
标识
DOI:10.1016/j.cmet.2020.03.008
摘要
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.
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