Ник Лэйн - Вопрос жизни [Энергия, эволюция и происхождение сложности]

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., Glé min, 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., Glé min, 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 (MAP 3 K 4 ) 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).

Температура и скорость метаболизма

Clarke, A., and H.-A. Pö rtner Temperature, metabolic power and the evolution of endothermy // Biological Reviews 85: 703–727 (2010).

Митохондриальные заболевания

Lane, N. Powerhouse of disease // Nature 440: 600–602 (2006).

Schon, E. A., DiMauro, S., and M. Hirano Human mitochondrial DNA: roles of inherited and somatic mutations // Nature Reviews Genetics 13: 878–890 (2012).

Wallace, D. C. A mitochondrial bioenergetic etiology of disease // Journal of Clinical Investigation 123: 1405–1412 (2013).

Zeviani, M, and V. Carelli Mitochondrial disorders // Current Opinion in Neurology 20: 564–571 (2007).

Цитоплазматическая мужская стерильность

Chen, L., and Y. G. Liu Male sterility and fertility restoration in crops // Annual Review Plant Biology 65: 579–606 (2014).

Innocenti, P., Morrow, E. H., and D. K. Dowling Experimental evidence supports a sex-specific selective sieve in mitochondrial genome evolution // Science 332: 845–848 (2011).

Sabar, M., Gagliardi, D., Balk, J., and C. J. Leaver ORFB is a subunit of F 1 F O -ATP synthase: insight into the basis of cytoplasmic male sterility in sunflower // EMBO Reports 4: 381–386 (2003).

Правило Холдейна и птицы

Hill, G. E., and J. D. Johnson The mitonuclear compatibility hypothesis of sexual selection // Proc. R. Soc. B 280: 20131314 (2013).

Mittwoch, U. Phenotypic manifestations during the development of the dominant and default gonads in mammals and birds // Journal of Experimental Zoology 281: 466–471 (1998).

Что нужно для полета

Suarez, R. K. Oxygen and the upper limits to animal design and performance // Journal of Experimental Biology 201: 1065–1072 (1998).

Апоптотический порог

Lane, N. Bioenergetic constraints on the evolution of complex life // Cold Spring Harbor Perspectives in Biology, doi: 10.1101/cshperspect.a015982 (2014).

Lane, N. The costs of breathing // Science 334: 184–185 (2011).

Скрытый выкидыш на ранних стадиях у людей

Van Blerkom, J., Davis, P. W., and J. Lee ATP content of human oocytes and developmental potential and outcome after in-vitro fertilization and embryo transfer // Human Reproduction 10: 415–424 (1995).

Zinaman, M. J., O’Connor, J., Clegg, E. D., Selevan, S. G., and C. C. Brown Estimates of human fertility and pregnancy loss // Fertility and Sterility 65: 503–509 (1996).

Свободнорадикальная теория старения

Barja, G. Updating the mitochondrial free-radical theory of aging: an integrated view, key aspects, and confounding concepts // Antioxidants and Redox Signalling 19: 1420–1445 (2013).

Gerschman, R., Gilbert, D. L., Nye, S. W., Dwyer, P., and W. O. Fenn Oxygen poisoning and X irradiation: a mechanism in common // Science 119: 623–626 (1954).

Harmann, D. Aging – a theory based on free-radical and radiation chemistry // Journal of Gerontology 11: 298–300 (1956).

Murphy, M. P. How mitochondria produce reactive oxygen species // Biochemical Journal 417: 1–13 (2009).

Проблемы свободнорадикальной теории старения

Bjelakovic, G., Nikolova, D., Gluud, L. L., Simonetti, R. G., and C. Gluud Antioxidant supplements for prevention of mortality in healthy participants and patients with various diseases // Cochrane Database of Systematic Reviews, doi: 10.1002/14651858. CD007176 (2008).

Gutteridge, J. M. C., and B. Halliwell Antioxidants: Molecules, medicines, and myths // Biochemical Biophysical Research Communications 393: 561–564 (2010).

Gnaiger, E., Mendez, G., and S. C. Hand High phosphorylation efficiency and depression of uncoupled respiration in mitochondria under hypoxia // Proceedings National Academy Sciences 97: 11080–11085 (2000).

Moyer, M. W. The myth of antioxidants // Scientific American 308: 62–67 (2013).

Свободнорадикальная сигнализация при старении

Lane, N. Mitonuclear match: optimizing fitness and fertility over generations drives ageing within generations // BioEssays 33: 860–869 (2011).

Moreno-Loshuertos, R., Acin-Perez, R., Fernandez-Silva, P., Movilla, N., Perez-Martos, A., de Cordoba S. R., Gallardo, M. E., and J. A. Enriquez Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants // Nature Genetics 38: 1261–1268 (2006).

Sobek, S., Rosa, I. D., Pommier, Y.,et al. Negative regulation of mitochondrial transcrioption by mitochondrial topoisomerase I // Nucleic Acids Research 41: 9848–9857 (2013).

Свободные радикалы в контексте теории скорости жизни

Barja, G. Mitochondrial oxygen consumption and reactive oxygen species production are independently modulated: implications for aging studies // Rejuvenation Research 10: 215–224 (2007).

Boveris, A., and B. Chance Mitochondrial generation of hydrogen peroxide – general properties and effect of hyperbaric oxygen // Biochemical Journal 134: 707–716 (1973).

Pearl, R. The Rate of Living. Being an Account of some Experimental Studies on the Biology of Life Duration . University of London Press, London (1928).

Свободные радикалы и болезни пожилого возраста

Desler, C., Marcker, M. L., Singh, K. K., and L. J. Rasmussen The importance of mitochondrial DNA in aging and cancer // Journal of Aging Research 2011: 407536 (2011).

Halliwell, B., and J. M. C. Gutteridge Free Radicals in Biology and Medicine . 4 thedn. Oxford University Press, Oxford (2007).

He, Y., Wu, J., Dressman, D. C.,et al. Heteroplasmic mitochondrial DNA mutations in normal and tumour cells // Nature 464: 610–614 (2010).

Lagouge, M., and N.-G. Larsson The role of mitochondrial DNA mutations and free radicals in disease and ageing // Journal of Internal Medicine 273: 529–543 (2013).

Lane, N. A unifying view of aging and disease: the double agent theory // Journal of Theoretical Biology 225: 531–540 (2003).

Moncada, S., Higgs, A. E., and S. L. Colombo Fulfilling the metabolic requirements for cell proliferation // Biochemical Journal 446: 1–7 (2012).

Аэробная производительность и срок жизни

Bennett, A. F., and J. A. Ruben Endothermy and activity in vertebrates // Science 206: 649–654 (1979).

Bramble, D. M., and D. E. Lieberman Endurance running and the evolution of Homo // Nature 432: 345–352 (2004).

Koch, L. G., Kemi, O. J., Qi, N.,et al. Intrinsic aerobic capacity sets a divide for aging and longevity // Circulation Research 109: 1162–1172 (2011).

Wislø ff, U., Najjar, S. M., Ellingsen, O.,et al. Cardiovascular risk factors emerge after artificial selection for low aerobic capacity // Science 307: 418–420 (2005).

Прокариота или эукариота?

Wujek, D. E. Intracellular bacteria in the blue-green-alga Pleurocapsa minor // Transactions American Microscopical Society 98: 143–145 (1979).

Yamaguchi, M., Mori, Y., Kozuka, Y.,et al. Prokaryote or eukaryote? A unique organism from the deep sea // Journal of Electron Microscopy 61: 423–431 (2012).