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Evolution and Physiological Roles of Phosphagen Systems
Abstract
▪ Abstract Phosphagens are phosphorylated guanidino compounds that are linked to energy state and ATP hydrolysis by corresponding phosphagen kinase reactions: phosphagen + MgADP + H+↔ guanidine acceptor + MgATP. Eight different phosphagens (and corresponding phosphagen kinases) are found in the animal kingdom distributed along distinct phylogenetic lines. By far, the creatine phosphate/creatine kinase (CP/CK) system, which is found in the vertebrates and is widely distributed throughout the lower chordates and invertebrates, is the most extensively studied phosphagen system. Phosphagen kinase reactions function in temporal ATP buffering, in regulating inorganic phosphate (Pi) levels, which impacts glycogenolysis and proton buffering, and in intracellular energy transport. Phosphagen kinase reactions show differences in thermodynamic poise, and the phosphagens themselves differ in terms of certain physical properties including intrinsic diffusivity. This review evaluates the distribution of phosphagen systems and tissue-specific expression of certain phosphagens in an evolutionary and functional context. The role of phosphagens in regulation of intracellular Pi levels likely evolved early. Thermodynamic poise of the phosphagen kinase reaction profoundly impacts this capacity. Furthermore, it is hypothesized that the capacity for intracellular targeting of CK evolved early as a means of facilitating energy transport in highly polarized cells and was subsequently exploited for temporal ATP buffering and dynamic roles in metabolic regulation in cells displaying high and variable rates of aerobic energy production.
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Cites
Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock
Doolittle, R. F., Feng, D.-F., Tsang, S., Cho, G., & Little, E. (1996) · Science · doi:10.1126/science.271.5248.470 · Cited by 581
Physiological and metabolic responses to hypoxia in invertebrates
Grieshaber, M. K., Hardewig, I., Kreutzer, U., & Pörtner, H.-O. (1993) · Reviews of Physiology, Biochemistry and Pharmacology · doi:10.1007/bfb0030909 · Cited by 398
Wallimann, T., Dolder, M., Schlattner, U., Eder, M., Hornemann, T., O'Gorman, E., Rück, A., & Brdiczka, D. (1998) · BioFactors · doi:10.1002/biof.5520080310 · Cited by 230
‘Hot spots’ of creatine kinase localization in brain: cerebellum, hippocampus and choroid plexus
Kaldis, P., Hemmer, W., Zanolla, E., Holtzman, D., & Wallimann, T. (2009) · Developmental Neuroscience · doi:10.1159/000111452 · Cited by 99
Cited by
Creatine: Endogenous Metabolite, Dietary, and Therapeutic Supplement
Brosnan, J. T., & Brosnan, M. E. (2007) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.27.061406.093621 · Cited by 347
Synthesis and transport of creatine in the CNS: Importance for cerebral functions
Béard, E., & Braissant, O. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06935.x · Cited by 192
Schlattner, U., Klaus, A., Ramirez Rios, S., Guzun, R., Kay, L., & Tokarska-Schlattner, M. (2016) · Amino Acids · doi:10.1007/s00726-016-2267-3 · Cited by 96
The advantage of channeling nucleotides for very processive functions
Zala, D., Schlattner, U., Desvignes, T., Bobe, J., Roux, A., Chavrier, P., & Boissan, M. (2017) · F1000Research · doi:10.12688/f1000research.11561.2 · Cited by 79
Evolution and divergence of the genes for cytoplasmic, mitochondrial, and flagellar creatine kinases
Suzuki, T., Mizuta, C., Uda, K., Ishida, K., Mizuta, K., Sona, S., Compaan, D. M., & Ellington, W. R. (2004) · Journal of Molecular Evolution · doi:10.1007/s00239-004-2615-x · Cited by 43
Metadata
- Authors
- Ellington, W. R.
- Venue
- Annual Review of Physiology
- Publisher
- Annual Reviews
- Published
- 2001-03
- Volume
- 63
- Issue
- 1
- Pages
- 289-325
- ISSN
- 0066-4278 (ISSN-L)
- 1545-1585
- OpenAlex
- W2144699036
- Cited by
- 517
- References
- 4
- FWCI
- 0.94
- Type
- journal article
- Language
- en
- Open access
- closed
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