Academic Journal

The conversion of formate into purines stimulates mTORC1 leading to CAD-dependent activation of pyrimidine synthesis

التفاصيل البيبلوغرافية
العنوان: The conversion of formate into purines stimulates mTORC1 leading to CAD-dependent activation of pyrimidine synthesis
المؤلفون: Jacqueline Tait-Mulder, Kelly Hodge, David Sumpton, Sara Zanivan, Alexei Vazquez
المصدر: Cancer & Metabolism, Vol 8, Iss 1, Pp 1-10 (2020)
بيانات النشر: BMC
سنة النشر: 2020
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Background Mitochondrial serine catabolism to formate induces a metabolic switch to a hypermetabolic state with high rates of glycolysis, purine synthesis and pyrimidine synthesis. While formate is a purine precursor, it is not clear how formate induces pyrimidine synthesis. Methods Here we combine phospho-proteome and metabolic profiling to determine how formate induces pyrimidine synthesis. Results We discover that formate induces phosphorylation of carbamoyl phosphate synthetase (CAD), which is known to increase CAD enzymatic activity. Mechanistically, formate induces mechanistic target of rapamycin complex 1 (mTORC1) activity as quantified by phosphorylation of its targets S6, 4E-BP1, S6K1 and CAD. Treatment with the allosteric mTORC1 inhibitor rapamycin abrogates CAD phosphorylation and pyrimidine synthesis induced by formate. Furthermore, we show that the formate-dependent induction of mTOR signalling and CAD phosphorylation is dependent on an increase in purine synthesis. Conclusions We conclude that formate activates mTORC1 and induces pyrimidine synthesis via the mTORC1-dependent phosphorylation of CAD.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 2049-3002
Relation: http://link.springer.com/article/10.1186/s40170-020-00228-3; https://doaj.org/toc/2049-3002; https://doaj.org/article/3b75c2ea9e3f4616aa20135e76721224
DOI: 10.1186/s40170-020-00228-3
الاتاحة: https://doi.org/10.1186/s40170-020-00228-3
https://doaj.org/article/3b75c2ea9e3f4616aa20135e76721224
رقم الانضمام: edsbas.1517DDA2
قاعدة البيانات: BASE
الوصف
تدمد:20493002
DOI:10.1186/s40170-020-00228-3