Preview

Vavilov Journal of Genetics and Breeding

Advanced search

A Drosophila melanogaster mitotype may have an adaptive meaning

https://doi.org/10.18699/VJ19.504

Abstract

Several different mitochondrial clades have been found in natural populations of Drosophila melanogaster. Most often, the difference is in single nucleotide substitutions, some of which are conservative. Some clades are rare, and others dominate. It has been reported that clade III dominates over clades V and VI in seven populations of D. melanogaster. We compared D. melanogaster strains with different mitotypes by locomotor activity (using TriKinetics Drosophila Activity Monitor), energy expenditure (by indirect calorimetry, based on measuring oxygen consumption) and life span (under extreme conditions at 29 °C). The nuclear genomes of these strains were aligned for several generations by backcrosses. According to our data, individuals with the mitotype from clade III had a higher level of locomotor activity and longer life span. In terms of energy expenditure, the strains studied did not differ. However, the same level of energy expenditure may be differently distributed between the state of activity and the state of rest or sleep. If the energy expenditure during the sleep in flies with different locomotor activity is the same, then an individual with the same overall energy expenditure can move a greater distance or be active longer. This can be interpreted as an advantage of the strain with the mitotype from clade III compared to the other two mitotypes studied. If individuals have different energy expenditure values at rest, the strains with lower energy expenditure at rest spend less energy during forced inactivity. In this case, the mitotype from clade III should also be advantageous. What nucleotide substitutions in the mitotype from clade III can provide an adaptive advantage is not clear yet. We assume that individuals with widespread clade М(III) may have adaptive advantages compared to other mitotypes due to their greater locomotor activity even with the same energy expenditure. Further studies are required, for mitotypes are polymorphic for single nucleotide polymorphism not only between but also within the clades.

About the Authors

D. V. Petrovskii
Institute of Cytology and Genetics, SB RAS; Institute of Systematics and Ecology of Animals, SB RAS
Russian Federation


L. P. Zakharenko
Institute of Cytology and Genetics, SB RAS; Novosibirsk State University
Russian Federation


References

1. Bland J.M., Altman D.G. The logrank test. The BMJ. 2004;328:1073- 1074. Clancy D.J. Variation in mitochondrial genotype has substantial lifespan effects which may be modulated by nuclear background. Aging Cell. 2008;7(6):795-804. DOI 10.1111/j.1474-9726.2008. 00428.x.

2. Diarra G.M., Roberts T.W., Christensen B.M. Automated measurement of oxygen consumption by the yellow fever mosquito, Aedes aegypti. Am. J. Trop. Med. Hyg. 1999;60:859-864.

3. Early A.M., Clark A.G. Monophyly of Wolbachia pipientis genomes within Drosophila melanogaster: geographic structuring, titre variation and host effects across five populations. Mol. Ecol. 2013;23: 5765-5778. DOI 10.1111/mec.12530.

4. Gruntenko N.Е., Ilinsky Y.Y., Adonyeva N.V., Burdina E.V., Bykov R.A., Menshanov P.N., Rauschenbach I.Y. Various Wolbachia genotypes differently influence host Drosophila dopamine metabolism and survival under heat stress conditions. BMC Evol. Biol. 2017;17(Suppl. 2):252. DOI 10.1186/s12862-017-1104-y.

5. Halliwell B. Free radicals and antioxidants: updating a personal view. Nutr. Rev. 2012;70:257-265. DOI 10.1111/j.1753-4887.2012. 00476.x.

6. Harman D. Aging: a theory based on free radical and radiation chemistry. J. Gerontol. 1956;11:298-300. DOI 10.1093/geronj/11.3.298.

7. Ilinsky Y. Coevolution of Drosophila melanogaster mtDNA and Wolbachia genotypes. PLoS One. 2013;8(1):e54373. DOI 10.1371/journal.pone.0054373.

8. Ilinsky Yu.Yu., Bykov R.A., Zakharov I.K. Cytotypes of mutant Drosophila melanogaster stocks from the collection of the genetics of population laboratory of the Institute of Cytology and Genetics sb ras: genotypes of the Wolbachia endosymbiont and host mitotypes. Vavilovskii Zhurnal Genetiki i Selektsii = Vavilov Journal of Genetics and Breeding. 2013;17:407-415. (in Russian)

9. Katewa S.D., Ballard J.W. Sympatric Drosophila simulans flies with distinct mtDNA show difference in mitochondrial respiration and electron transport. Insect Biochem. Mol. Biol. 2007;37(3):213-222.

10. Lehmann G., Segal E., Muradian K.K., Fraifeld V.E. Do mitochondrial DNA and metabolic rate complement each other in determination of the mammalian maximum longevity? Rejuvenation Res. 2008; 11:409-417.

11. Maklakov A.A., Friberg U., Dowling D.K., Arnqvist G. Within-population variation in cytoplasmic genes affects female life span and aging in Drosophila melanogaster. Evolution. 2006;60:2081-2086.

12. Melvin R.G., Van Voorhies W.A., Ballard J.W. Working harder to stay alive: metabolic rate increases with age in Drosophila simulans but does not correlate with life span. J. Insect Physiol. 2007;53: 1300-1306.

13. Min K.T., Benzer S. Wolbachia, normally a symbiont of Drosophila, can be virulent, causing degeneration and early death. Proc. Natl. Acad. Sci. USA. 1997;94:10792-10796.

14. Muradian K.K., Lehmann G., Fraifeld V.E. NUMT (“new mighty”) hypothesis of longevity. Rejuvenation Res. 2010;13:152-155. DOI 10.1089/rej.2009.0974.

15. Richardson M.F., Weinert L.A., Welch J.J., Linheiro R.S., Magwire M.M., Jiggins F.M., Bergman C.M. Population genomics of the Wolbachia endosymbiont in Drosophila melanogaster. PLoS Genet. 2012;8(12):e1003129. DOI 10.1371/journal.pgen.1003129.

16. Rottenberg H. Coevolution of exceptional longevity, exceptionally high metabolic rates, and mitochondrial DNA-coded proteins in mammals. Exp. Gerontol. 2007;42(4):364-373.

17. Schmidt-Nielsen K. Animal Physiology: Adaptation and Environment. London–New York, Cambridge University Press, 1975. (Russ. ed. Schmidt-Nielsen K. Animal Physiology: Adaptation and Environment. Book 1. Moscow: Mir Publ., 1982). (in Russian)

18. Stuart J.A., Brown M.F. Mitochondrial DNA maintenance and bioenergetics. Biochim. Biophys. Acta. 2006;1757(2):79-89.

19. Zhu C.T., Ingelmo P., Rand D.M. G×G×E for lifespan in Drosophila: mitochondrial, nuclear, and dietary interactions that modify longevity. PLoS Genet. 2014;10(5):e1004354. DOI 10.1371/journal. pgen.1004354.


Review

Views: 689


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2500-3259 (Online)