Ознакомительная версия. Доступно 20 страниц из 99
Lane, N. Power, Sex, Suicide: Mitochondria and the Meaning of Life. Oxford University Press, Oxford (2005).
Скорость митохондриального мутагенеза у животных, растений и базальных метазоев
Galtier, N. The intriguing evolutionary dynamics of plant mitochondrial DNA // BMC Biology 9: 61 (2011).
Huang, D., Meier, R., Todd, P. A., and L. M. Chou Slow mitochondrial COI sequence evolution at the base of the metazoan tree and its implications for DNA barcoding // Journal of Molecular Evolution 66: 167–174 (2008).
Lane, N. On the origin of barcodes // Nature 462: 272–274 (2009).
Linnane, A. W., Ozawa, T., Marzuki, S., and M. Tanaka Mitochondrial DNA mutations as an important contributor to ageing and degenerative disease // Lancet 333: 642–645 (1989).
Pesole, G., Gissi, C., De Chirico, A., and C. Saccone Nucleotide substitution rate of mammalian mitochondrial genomes // Journal of Molecular Evolution 48: 427–434 (1999).
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).
Allen, J. F. Separate sexes and the mitochondrial theory of ageing // Journal of Theoretical Biology 180: 135–140 (1996).
Buss, L. The Evolution of Individuality. Princeton University Press, Princeton (1987).
Clark, W. R. Sex and the Origins of Death. Oxford University Press, New York (1997).
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
Allen, J. F. The function of genomes in bioenergetic organelles // Phil. Trans. R. Soc. B 358: 19–37 (2003).
Lane, N. The costs of breathing // Science 334: 184–185 (2011).
Moser, C. C., Page, C. C., and P. L. Dutton Darwin at the molecular scale: selection and variance in electron tunnelling proteins including cytochrome c oxidase // Phil. Trans. R. Soc. B 361: 1295–1305 (2006).
Schatz, G., and T. L. Mason The biosynthesis of mitochondrial proteins // Annual Review Biochemistry 43: 51–87 (1974).
Vinothkumar, K. R., Zhu, J., and J. Hirst Architecture of the mammalian respiratory complex I // Nature 515: 80–84 (2014).
Гибридное разрушение, цибриды и происхождение видов
Barrientos, A., Kenyon, L., and C. T. Moraes Human xenomitochondrial cybrids. Cellular models of mitochondrial complex I deficiency // Journal of Biological Chemistry 273: 14210–14217 (1998).
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).
Burton, R. S., and F. S. Barreto A disproportionate role for mtDNA in Dobzhansky – Muller incompatibilities? // Molecular Ecology 21: 4942–4957 (2012).
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).
Lane, N. On the origin of barcodes // Nature 462: 272–274 (2009).
Митохондриальный контроль апоптоза
Hengartner, M. O. Death cycle and Swiss army knives // Nature 391: 441–442 (1998).
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).
Lane, N. On the origin of barcodes // Nature 462: 272–274 (2009).
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
Coyne, J. A., and H. A. Orr Speciation. Sinauer Associates, Sunderland MA (2004).
Haldane, J. B. S. Sex ratio and unisexual sterility in hybrid animals // Journal of Genetics 12: 101–109 (1922).
Johnson, N. A. Haldane’s rule: the heterogametic sex // Nature Education 1: 58 (2008).
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).
Mittwoch, U. Sex determination // EMBO Reports 14: 588–592 (2013).
Mittwoch, U. The elusive action of sex-determining genes: mitochondria to the rescue? // Journal of Theoretical Biology 228: 359–365 (2004).
Ознакомительная версия. Доступно 20 страниц из 99
