Literature DB >> 26567272

Division of labour: how does folate metabolism partition between one-carbon metabolism and amino acid oxidation?

Margaret E Brosnan1, Luke MacMillan1, Jennifer R Stevens1, John T Brosnan2.   

Abstract

One-carbon metabolism is usually represented as having three canonical functions: purine synthesis, thymidylate synthesis and methylation reactions. There is however a fourth major function: the metabolism of some amino acids (serine, glycine, tryptophan and histidine), as well as choline. These substrates can provide cells with more one-carbon groups than they need for these three canonical functions. Therefore, there must be mechanisms for the disposal of these one-carbon groups (when in excess) which maintain the complement of these groups required for the canonical functions. The key enzyme for these mechanisms is 10-formyl-THF (tetrahydrofolate) dehydrogenase (both mitochondrial and cytoplasmic isoforms) which oxidizes the formyl group to CO2 with the attendant reduction of NADP(+) to NADPH and release of THF. In addition to oxidizing the excess of these compounds, this process can reduce substantial quantities of NADP(+) to NADPH.
© 2015 Authors; published by Portland Press Limited.

Entities:  

Keywords:  NADPH; S-adenosylmethionine; folate; formate; glycine metabolism; serine neogenesis

Mesh:

Substances:

Year:  2015        PMID: 26567272     DOI: 10.1042/BJ20150837

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  30 in total

Review 1.  Serine and one-carbon metabolism in cancer.

Authors:  Ming Yang; Karen H Vousden
Journal:  Nat Rev Cancer       Date:  2016-09-16       Impact factor: 60.716

Review 2.  One-Carbon Metabolism in Health and Disease.

Authors:  Gregory S Ducker; Joshua D Rabinowitz
Journal:  Cell Metab       Date:  2016-09-15       Impact factor: 27.287

3.  Metabolic Reprogramming by Folate Restriction Leads to a Less Aggressive Cancer Phenotype.

Authors:  Zahra Ashkavand; Ciara O'Flanagan; Mirko Hennig; Xiuxia Du; Stephen D Hursting; Sergey A Krupenko
Journal:  Mol Cancer Res       Date:  2017-02       Impact factor: 5.852

4.  Plasma Formate Is Greater in Fetal and Neonatal Rats Compared with Their Mothers.

Authors:  Margaret E Brosnan; Garrett Tingley; Luke MacMillan; Brian Harnett; Theerawat Pongnopparat; Jenika D Marshall; John T Brosnan
Journal:  J Nutr       Date:  2020-05-01       Impact factor: 4.798

Review 5.  Loss of ALDH1L1 folate enzyme confers a selective metabolic advantage for tumor progression.

Authors:  Sergey A Krupenko; Natalia I Krupenko
Journal:  Chem Biol Interact       Date:  2019-02-20       Impact factor: 5.192

6.  Lifestyle, metabolite, and genetic determinants of formate concentrations in a cross-sectional study in young, healthy adults.

Authors:  John T Brosnan; James L Mills; Per M Ueland; Barry Shane; Ruzong Fan; Chi-Yang Chiu; Faith Pangilinan; Lawrence C Brody; Margaret E Brosnan; Theerawat Pongnopparat; Anne M Molloy
Journal:  Am J Clin Nutr       Date:  2018-03-01       Impact factor: 7.045

7.  Riboflavin Deficiency in Rats Decreases de novo Formate Production but Does Not Affect Plasma Formate Concentration.

Authors:  Luke MacMillan; Simon G Lamarre; Robin P daSilva; René L Jacobs; Margaret E Brosnan; John T Brosnan
Journal:  J Nutr       Date:  2017-01-25       Impact factor: 4.798

8.  Two-carbon folate cycle of commensal Lactobacillus reuteri 6475 gives rise to immunomodulatory ethionine, a source for histone ethylation.

Authors:  Daniel Röth; Abby J Chiang; Weidong Hu; Gabriel B Gugiu; Christina N Morra; James Versalovic; Markus Kalkum
Journal:  FASEB J       Date:  2018-11-19       Impact factor: 5.191

9.  Histidine Metabolism and Function.

Authors:  Margaret E Brosnan; John T Brosnan
Journal:  J Nutr       Date:  2020-10-01       Impact factor: 4.798

Review 10.  Creatine kinase in ischemic and inflammatory disorders.

Authors:  David Kitzenberg; Sean P Colgan; Louise E Glover
Journal:  Clin Transl Med       Date:  2016-08-15
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