| Literature DB >> 26924217 |
Joni Nikkanen1, Saara Forsström1, Liliya Euro1, Ilse Paetau1, Rebecca A Kohnz2, Liya Wang3, Dmitri Chilov1, Jenni Viinamäki4, Anne Roivainen5, Päivi Marjamäki6, Heidi Liljenbäck5, Sofia Ahola1, Jana Buzkova1, Mügen Terzioglu1, Nahid A Khan1, Sini Pirnes-Karhu1, Anders Paetau7, Tuula Lönnqvist8, Antti Sajantila4, Pirjo Isohanni9, Henna Tyynismaa10, Daniel K Nomura2, Brendan J Battersby1, Vidya Velagapudi11, Christopher J Carroll12, Anu Suomalainen13.
Abstract
Mitochondrial dysfunction affects cellular energy metabolism, but less is known about the consequences for cytoplasmic biosynthetic reactions. We report that mtDNA replication disorders caused by TWINKLE mutations-mitochondrial myopathy (MM) and infantile onset spinocerebellar ataxia (IOSCA)-remodel cellular dNTP pools in mice. MM muscle shows tissue-specific induction of the mitochondrial folate cycle, purine metabolism, and imbalanced and increased dNTP pools, consistent with progressive mtDNA mutagenesis. IOSCA-TWINKLE is predicted to hydrolyze dNTPs, consistent with low dNTP pools and mtDNA depletion in the disease. MM muscle also modifies the cytoplasmic one-carbon cycle, transsulfuration, and methylation, as well as increases glucose uptake and its utilization for de novo serine and glutathione biosynthesis. Our evidence indicates that the mitochondrial replication machinery communicates with cytoplasmic dNTP pools and that upregulation of glutathione synthesis through glucose-driven de novo serine biosynthesis contributes to the metabolic stress response. These results are important for disorders with primary or secondary mtDNA instability and offer targets for metabolic therapy.Entities:
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Year: 2016 PMID: 26924217 DOI: 10.1016/j.cmet.2016.01.019
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287