A computational model of mitochondrial deoxynucleotide metabolism and DNA replication. Export

@article{citeulike:2480433, abstract = {We present a computational model of mitochondrial deoxynucleotide metabolism and mitochondrial DNA (mtDNA) synthesis. The model includes the transport of deoxynucleosides and deoxynucleotides into the mitochondrial matrix space, as well as their phosphorylation and polymerization into mtDNA. Different simulated cell types (cancer, rapidly dividing, slowly dividing, and postmitotic cells) are represented in this model by different cytoplasmic deoxynucleotide concentrations. We calculated the changes in deoxynucleotide concentrations within the mitochondrion during the course of a mtDNA replication event and the time required for mtDNA replication in the different cell types. On the basis of the model, we define three steady states of mitochondrial deoxynucleotide metabolism: the phosphorylating state (the net import of deoxynucleosides and export of phosphorylated deoxynucleotides), the desphosphorylating state (the reverse of the phosphorylating state), and the efficient state (the net import of both deoxynucleosides and deoxynucleotides). We present five testable hypotheses based on this simulation. First, the deoxynucleotide pools within a mitochondrion are sufficient to support only a small fraction of even a single mtDNA replication event. Second, the mtDNA replication time in postmitotic cells is much longer than that in rapidly dividing cells. Third, mitochondria in dividing cells are net sinks of cytoplasmic deoxynucleotides, while mitochondria in postmitotic cells are net sources. Fourth, the deoxynucleotide carrier exerts the most control over the mtDNA replication rate in rapidly dividing cells, but in postmitotic cells, the NDPK and TK2 enzymes have the most control. Fifth, following from the previous hypothesis, rapidly dividing cells derive almost all of their mtDNA precursors from the cytoplasmic deoxynucleotides, not from phosphorylation within the mitochondrion.}, address = {Virginia Bioinformatics Institute, Virginia Polytechnic and State Univ., Bioinformatics Facility I (0477 Blacksburg, VA 24061, USA.}, author = {Bradshaw, P. C. and Samuels, D. C.}, citeulike-article-id = {2480433}, citeulike-linkout-0 = {http://dx.doi.org/10.1152/ajpcell.00530.2004}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/15634740}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=15634740}, doi = {10.1152/ajpcell.00530.2004}, issn = {0363-6143}, journal = {Am J Physiol Cell Physiol}, keywords = {aging, computational, mitochondria, model}, month = {May}, number = {5}, posted-at = {2008-03-06 21:16:42}, priority = {3}, title = {A computational model of mitochondrial deoxynucleotide metabolism and DNA replication.}, url = {http://dx.doi.org/10.1152/ajpcell.00530.2004}, volume = {288}, year = {2005} }

TY - JOUR ID - citeulike:2480433 L3 - citeulike-article-id:2480433 N2 - We present a computational model of mitochondrial deoxynucleotide metabolism and mitochondrial DNA (mtDNA) synthesis. The model includes the transport of deoxynucleosides and deoxynucleotides into the mitochondrial matrix space, as well as their phosphorylation and polymerization into mtDNA. Different simulated cell types (cancer, rapidly dividing, slowly dividing, and postmitotic cells) are represented in this model by different cytoplasmic deoxynucleotide concentrations. We calculated the changes in deoxynucleotide concentrations within the mitochondrion during the course of a mtDNA replication event and the time required for mtDNA replication in the different cell types. On the basis of the model, we define three steady states of mitochondrial deoxynucleotide metabolism: the phosphorylating state (the net import of deoxynucleosides and export of phosphorylated deoxynucleotides), the desphosphorylating state (the reverse of the phosphorylating state), and the efficient state (the net import of both deoxynucleosides and deoxynucleotides). We present five testable hypotheses based on this simulation. First, the deoxynucleotide pools within a mitochondrion are sufficient to support only a small fraction of even a single mtDNA replication event. Second, the mtDNA replication time in postmitotic cells is much longer than that in rapidly dividing cells. Third, mitochondria in dividing cells are net sinks of cytoplasmic deoxynucleotides, while mitochondria in postmitotic cells are net sources. Fourth, the deoxynucleotide carrier exerts the most control over the mtDNA replication rate in rapidly dividing cells, but in postmitotic cells, the NDPK and TK2 enzymes have the most control. Fifth, following from the previous hypothesis, rapidly dividing cells derive almost all of their mtDNA precursors from the cytoplasmic deoxynucleotides, not from phosphorylation within the mitochondrion. IS - 5 JF - Am J Physiol Cell Physiol SN - 0363-6143 AD - Virginia Bioinformatics Institute, Virginia Polytechnic and State Univ., Bioinformatics Facility I (0477 Blacksburg, VA 24061, USA. TI - A computational model of mitochondrial deoxynucleotide metabolism and DNA replication. VL - 288 KW - aging KW - computational KW - mitochondria KW - model AU - Bradshaw, PC AU - Samuels, DC PY - 2005/05// UR - http://dx.doi.org/10.1152/ajpcell.00530.2004 ER -