| Literature DB >> 30184506 |
Wei-Cheng Lin1, Archan Chakraborty2, Shih-Chia Huang3, Pei-Yu Wang1, Ya-Ju Hsieh4, Kun-Yi Chien5, Yen-Hsien Lee6, Chia-Chun Chang7, Hsiang-Yu Tang8, Yu-Tsun Lin6, Chang-Shung Tung9, Ji-Dung Luo10, Ting-Wen Chen11, Tzu-Yang Lin12, Mei-Ling Cheng13, Yi-Ting Chen14, Chau-Ting Yeh15, Ji-Long Liu16, Li-Ying Sung17, Ming-Shi Shiao18, Jau-Song Yu19, Yu-Sun Chang20, Li-Mei Pai21.
Abstract
CTP synthase (CTPS) forms compartmentalized filaments in response to substrate availability and environmental nutrient status. However, the physiological role of filaments and mechanisms for filament assembly are not well understood. Here, we provide evidence that CTPS forms filaments in response to histidine influx during glutamine starvation. Tetramer conformation-based filament formation restricts CTPS enzymatic activity during nutrient deprivation. CTPS protein levels remain stable in the presence of histidine during nutrient deprivation, followed by rapid cell growth after stress relief. We demonstrate that filament formation is controlled by methylation and that histidine promotes re-methylation of homocysteine by donating one-carbon intermediates to the cytosolic folate cycle. Furthermore, we find that starvation stress and glutamine deficiency activate the GCN2/ATF4/MTHFD2 axis, which coordinates CTPS filament formation. CTPS filament formation induced by histidine-mediated methylation may be a strategy used by cancer cells to maintain homeostasis and ensure a growth advantage in adverse environments.Entities:
Keywords: ATF4; CTP synthase; CTPS filament; MTHFD2; cancer; folate cycle; histidine; methylation; nutrient deprivation; one carbon
Mesh:
Substances:
Year: 2018 PMID: 30184506 DOI: 10.1016/j.celrep.2018.08.007
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423