Sun, Ren
- Department of Animal Biosciences, Swedish University of Agricultural Sciences
Research article2014Peer reviewed
Sun, Ren; Wang, Liya
Mitochondrial thymidine kinase 2 (TK2) is a nuclear gene-encoded protein, synthesized in the cytosol and subsequently translocated into the mitochondrial mateix, where it catalyzes the phosphorylation of thymidine (dT) and deoxycytidine (dC). The kinetics of dT phosphorylation exhibits negative cooperativity, but dC phosphorylation follows hyperbolic Michaelis-Menten kinetics. The two substrates compete with each other in that dT competitive inhibitor of dC phosphorylation, while dC acts as a noncompetitive inhibitor of dT phosphorylation. In addition, TK2 feedback inhibited by dTTP and dCTP TK2 also phosphorylates a number of pyrimidine nucleoside analgues used in antiviral and anticancer therapy and thus plays an important role in mitochondrial toxicies caused by nucleoside analogues. Deficiency in TK2 activity due to genetic alterations causes devastating mitochondrial diseases, which are characterized by mitochondrial DNA (mtDNA) depletion or multiple deletions in the affected tissues. Severe TK2 deficiency iks associated with early onset fatal mitochondrial DNA depletion syndrome, while less severe deficiencies result in late-onset phenotypes. In this review, studies of the enzyme kinetic behavior of TK2 enzyme variants are used to explain the mechanism of mtDNA depletion caused by TK2 mutation, thymidine overload due to thymidine phosphorylase deficiency, and mitochondrial toxicity caused by antiviral thymidine analogues.
thymidine kinase 2, thymidine phosphorylase, mitochondrial DNA depletion, mutations, enzyme kinetics
Biochemistry
2014, Volume: 53, number: 39, pages: 6142-6150
Biochemistry and Molecular Biology
Cell Biology
Cell and Molecular Biology
DOI: https://doi.org/10.1021/bi5006877
https://res.slu.se/id/publ/62165