Histidine-Dependent Protein Methylation Is Required for Compartmentalization of CTP Synthase

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...

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Veröffentlicht in:Cell reports (Cambridge) 2018-09, Vol.24 (10), p.2733-2745.e7
Hauptverfasser: Lin, Wei-Cheng, Chakraborty, Archan, Huang, Shih-Chia, Wang, Pei-Yu, Hsieh, Ya-Ju, Chien, Kun-Yi, Lee, Yen-Hsien, Chang, Chia-Chun, Tang, Hsiang-Yu, Lin, Yu-Tsun, Tung, Chang-Shung, Luo, Ji-Dung, Chen, Ting-Wen, Lin, Tzu-Yang, Cheng, Mei-Ling, Chen, Yi-Ting, Yeh, Chau-Ting, Liu, Ji-Long, Sung, Li-Ying, Shiao, Ming-Shi, Yu, Jau-Song, Chang, Yu-Sun, Pai, Li-Mei
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Sprache:eng
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Zusammenfassung: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. [Display omitted] •Histidine is essential and sufficient for CTPS filament formation during starvation•The enzymatic activity of CTPS is reduced when it is in a filamentous structure•The GCN2/ATF4/MTHFD2 stress response pathway coordinates CTPS filament formation•Histidine-mediated regulation of cytosolic folate cycle promotes protein methylation Metabolic enzymes form membraneless compartments to adapt to environmental changes. Lin et al. demonstrate that histidine catabolism coupled with the folate cycle contributes to methionine synthesis, which promotes protein methylation. This post-translational modification in turn induces CTPS filament formation to preserve CTPS but reduces its enzymatic activity under starvation.
ISSN:2211-1247
2211-1247
DOI:10.1016/j.celrep.2018.08.007