TY - JOUR KW - C13orf31 KW - Crohn's disease KW - FAMIN KW - LACC1 KW - Still's disease KW - immunometabolism KW - pH homeostasis KW - purine metabolism KW - purine nucleotide cycle KW - redox homeostasis AU - Cader ZM AU - Rodrigues R AU - West J AU - Sewell G AU - Md-Ibrahim M AU - Reikine S AU - Sirago G AU - Unger L AU - Inglesias-Romero A AU - Ramshorn K AU - Haag L AU - Saveljeva S AU - Ebel J AU - Rosenstiel P AU - Kaneider N AU - Lee J AU - Lawley T AU - Bradley A AU - Dougan G AU - Modis Y AU - Griffin J AU - Kaser A AB -

Mutations in FAMIN cause arthritis and inflammatory bowel disease in early childhood, and a common genetic variant increases the risk for Crohn's disease and leprosy. We developed an unbiased liquid chromatography-mass spectrometry screen for enzymatic activity of this orphan protein. We report that FAMIN phosphorolytically cleaves adenosine into adenine and ribose-1-phosphate. Such activity was considered absent from eukaryotic metabolism. FAMIN and its prokaryotic orthologs additionally have adenosine deaminase, purine nucleoside phosphorylase, and S-methyl-5'-thioadenosine phosphorylase activity, hence, combine activities of the namesake enzymes of central purine metabolism. FAMIN enables in macrophages a purine nucleotide cycle (PNC) between adenosine and inosine monophosphate and adenylosuccinate, which consumes aspartate and releases fumarate in a manner involving fatty acid oxidation and ATP-citrate lyase activity. This macrophage PNC synchronizes mitochondrial activity with glycolysis by balancing electron transfer to mitochondria, thereby supporting glycolytic activity and promoting oxidative phosphorylation and mitochondrial H and phosphate recycling.

BT - Cell C1 - https://www.ncbi.nlm.nih.gov/pubmed/31978345 DA - 01/2020 DO - 10.1016/j.cell.2019.12.017 IS - 2 J2 - Cell LA - eng N2 -

Mutations in FAMIN cause arthritis and inflammatory bowel disease in early childhood, and a common genetic variant increases the risk for Crohn's disease and leprosy. We developed an unbiased liquid chromatography-mass spectrometry screen for enzymatic activity of this orphan protein. We report that FAMIN phosphorolytically cleaves adenosine into adenine and ribose-1-phosphate. Such activity was considered absent from eukaryotic metabolism. FAMIN and its prokaryotic orthologs additionally have adenosine deaminase, purine nucleoside phosphorylase, and S-methyl-5'-thioadenosine phosphorylase activity, hence, combine activities of the namesake enzymes of central purine metabolism. FAMIN enables in macrophages a purine nucleotide cycle (PNC) between adenosine and inosine monophosphate and adenylosuccinate, which consumes aspartate and releases fumarate in a manner involving fatty acid oxidation and ATP-citrate lyase activity. This macrophage PNC synchronizes mitochondrial activity with glycolysis by balancing electron transfer to mitochondria, thereby supporting glycolytic activity and promoting oxidative phosphorylation and mitochondrial H and phosphate recycling.

PY - 2020 SP - 278 EP - 295.e23 T2 - Cell TI - FAMIN Is a Multifunctional Purine Enzyme Enabling the Purine Nucleotide Cycle. UR - 10.1016/j.cell.2019.12.017 VL - 180 SN - 1097-4172 ER -