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Скорость митохондриального мутагенеза у животных, растений и базальных метазоев

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Возникновение разделения на сому и зародышевую линию

Allen, J. F., and W. B. M. de Paula Mitochondrial genome function and maternal inheritance // Biochemical Society Transactions 41: 1298–1304 (2013).

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Radzvilavicius, A. L., Hadjivasiliou, Z., Pomiankowski, A., and N. Lane Mitochondrial variation drives the evolution of sexes and the germline-soma distinction // PloS Biol. 2016 Dec 20;14 (12): e2000410 (2016).

Глава 7. Сила и слава

“Мозаичная” дыхательная цепь

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Гибридное разрушение, цибриды и происхождение видов

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Blier, P. U., Dufresne, F., and R. S. Burton Natural selection and the evolution of mtDNA-encoded peptides: evidence for intergenomic co-adaptation // Trends in Genetics 17: 400–406 (2001).

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Burton, R. S., Ellison, C. K., and J. S. Harrison The sorry state of F2 hybrids: consequences of rapid mitochondrial DNA evolution in allopatric populations // American Naturalist 168 Supplement 6: S14–24 (2006).

Gershoni, M., Templeton, A. R., and D. Mishmar Mitochondrial biogenesis as a major motive force of speciation // Bioessays 31: 642–650 (2009).

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Митохондриальный контроль апоптоза

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Koonin, E. V., and L. Aravind Origin and evolution of eukaryotic apoptosis: the bacterial connection // Cell Death and Differentiation 9: 394–404 (2002).

Lane, N. Origins of death // Nature 453: 583–585 (2008).

Zamzami, N., and G. Kroemer The mitochondrion in apoptosis: how Pandora’s box opens // Nature Reviews Molecular Cell Biology 2: 67–71 (2001).

Быстрая эволюция митохондриальных генов у животных и приспособление к среде

Bazin, E., Glémin, S., and N. Galtier Population size dies not influence mitochondrial genetic diversity in animals // Science 312: 570–572 (2006).

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Nabholz, B., Glémin, S., and N. Galtier The erratic mitochondrial clock: variations of mutation rate, not population size, affect mtDNA diversity across birds and mammals // BMC Evolutionary Biology 9: 54 (2009).

Wallace, D. C. Bioenergetics in human evolution and disease: implications for the origins of biological compolexity and the missing genetic variation of common diseases // Phil. Trans. R. Soc. B 368: 20120267 (2013).

Отбор по митохондриальной ДНК в зародышевой линии

Fan, W., Waymire, K. G., Narula, N., et al. A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations // Science 319: 958–962 (2008).

Stewart, J. B., Freyer, C., Elson, J. L., Wredenberg, A., Cansu, Z., Trifunovic, A., and N.-G. Larsson Strong purifying selection in transmission of mammalian mitochondrial DNA // PloS Biology 6: e10 (2008).

Правило Холдейна

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Haldane, J. B. S. Sex ratio and unisexual sterility in hybrid animals // Journal of Genetics 12: 101–109 (1922).

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Роль митохондрий и скорости метаболизма в определении пола

Bogani, D., Siggers, P., Brixet, R., et al. Loss of mitogen-activated protein kinase kinase kinase 4 (MAP3K4) reveals a requirement for MAPK signalling in mouse sex determination // PLoS Biology 7: e1000196 (2009).

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Mittwoch, U. The elusive action of sex-determining genes: mitochondria to the rescue? // Journal of Theoretical Biology 228: 359–365 (2004).