Developmental aspects of respiratory chain from fetus to infancy

Seminars in Fetal and Neonatal Medicine

Volumn 16, Issue 4, 2011, Pages 175-180

  Yanicostas, Constantin ^a,b   Soussi Yanicostas, Nadia ^a,b   El Khoury, Riyad ^a,b   Bénit, Paule ^a,b   Rustin, Pierre ^a,b  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Energetic; Epigenetics; Fetal development; Mitochondria; Mitochondrial diseases; Oocyte

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; MITOCHONDRIAL DNA; REACTIVE OXYGEN METABOLITE; RNA DIRECTED DNA POLYMERASE INHIBITOR; ZIDOVUDINE;

CHILD DEVELOPMENT; DEVELOPMENTAL GENETICS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENERGY METABOLISM; ENERGY TRANSFER; ENVIRONMENTAL FACTOR; EPIGENETICS; HEREDITY; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; MITOCHONDRIAL GENETICS; MITOCHONDRIAL RESPIRATION; NONHUMAN; OXIDATIVE STRESS; PRENATAL DEVELOPMENT; PRENATAL DRUG EXPOSURE; RESPIRATORY CHAIN; REVIEW; SYMPTOMATOLOGY; TERATOGENICITY;

ELECTRON TRANSPORT; EPIGENESIS, GENETIC; FETAL DEVELOPMENT; HUMANS; INFANT; INFANT, NEWBORN; MITOCHONDRIA;

EID: 79959892537     PISSN: 1744165X     EISSN: 18780946     Source Type: Journal    
DOI: 10.1016/j.siny.2011.05.005     Document Type: Review

References (57)

1. Sutovsky P. Ubiquitin-dependent proteolysis in mammalian spermatogenesis, fertilization, and sperm quality control: killing three birds with one stone. Microsc Res Tech 2003, 61:88-102.
2. Wolff J.N., Gemmell N.J. Lost in the zygote: the dilution of paternal mtDNA upon fertilization. Heredity 2008, 101:429-434.
3. Schwartz M., Vissing J. Paternal inheritance of mitochondrial DNA. N Engl J Med 2002, 347:576-580.
4. Taylor R.W., McDonnell M.T., Blakely E.L., et al. Genotypes from patients indicate no paternal mitochondrial DNA contribution. Ann Neurol 2003, 54:521-524.
5. Filosto M., Mancuso M., Vives-Bauza C., et al. Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies. Ann Neurol 2003, 54:524-526.
6. Quintana-Murci L., Rotig A., Munnich A., et al. Mitochondrial DNA inheritance in patients with deleted mtDNA. J Med Genet 2001, 38. E28.
7. Hiendleder S. Mitochondrial DNA inheritance after SCNT. Adv Exp Med Biol 2007, 591:103-116.
8. Devreker F., Englert Y. In vitro development and metabolism of the human embryo up to the blastocyst stage. Eur J Obstet Gynecol Reprod Biol 2000, 92:51-56.
9. Wai T., Teoli D., Shoubridge E.A. The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes. Nat Genet 2008, 40:1484-1488.
10. Ottosen L.D., Hindkaer J., Husth M., et al. Observations on intrauterine oxygen tension measured by fibre-optic microsensors. Reprod Biomed Online 2006, 13:380-385.
11. Burton G.J., Jauniaux E., Charnock-Jones D.S. The influence of the intrauterine environment on human placental development. Int J Dev Biol 2010, 54:303-312.
12. Trimarchi J.R., Liu L., Porterfield D.M., et al. Oxidative phosphorylation-dependent and -independent oxygen consumption by individual preimplantation mouse embryos. Biol Reprod 2000, 62:1866-1874.
13. Van Blerkom J., Davis P., Alexander S. Differential mitochondrial distribution in human pronuclear embryos leads to disproportionate inheritance between blastomeres: relationship to microtubular organization, ATP content and competence. Hum Reprod 2000, 15:2621-2633.
14. Dumollard R., Duchen M., Carroll J. The role of mitochondrial function in the oocyte and embryo. Curr Top Dev Biol 2007, 77:21-49.
15. Dumollard R., Ward Z., Carroll J., et al. Regulation of redox metabolism in the mouse oocyte and embryo. Development 2007, 134:455-465.
16. Acton B.M., Jurisicova A., Jurisica I., et al. Alterations in mitochondrial membrane potential during preimplantation stages of mouse and human embryo development. Molec Hum Reprod 2004, 10:23-32.
17. Van Blerkom J. Mitochondria in early mammalian development. Semin Cell Dev Biol 2009, 20:354-364.
18. Van Blerkom J., Davis P. Mitochondrial signaling and fertilization. Molec Hum Reprod 2007, 13:759-770.
19. Larsson N.G., Wang J., Wilhelmsson H., et al. Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice. Nat Genet 1998, 18:231-236.
20. Johnson M.T., Mahmood S., Hyatt S.L., et al. Inactivation of the murine pyruvate dehydrogenase (Pdha1) gene and its effect on early embryonic development. Mol Genet Metab 2001, 74:293-302.
21. Li K., Li Y., Shelton J.M., et al. Cytochrome c deficiency causes embryonic lethality and attenuates stress-induced apoptosis. Cell 2000, 101:389-399.
22. Cui X.S., Li X.Y., Jeong Y.J., et al. Gene expression of cox5a, 5b, or 6b1 and their roles in preimplantation mouse embryos. Biol Reprod 2006, 74:601-610.
23. Jauniaux E., Watson A.L., Hempstock J., et al. Onset of maternal arterial blood flow and placental oxidative stress. A possible factor in human early pregnancy failure. Am J Pathol 2000, 157:2111-2122.
24. Frendo J.L., Therond P., Bird T., et al. Overexpression of copper zinc superoxide dismutase impairs human trophoblast cell fusion and differentiation. Endocrinology 2001, 142:3638-3648.
25. Faivre L., Cormier-Daire V., Chretien D., et al. Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency. Prenat Diagn 2000, 20:732-737.
26. Rustin P., Chretien D., Bourgeron T., et al. Biochemical and molecular investigations in respiratory chain deficiencies. Clin Chim Acta 1994, 228:35-51.
27. Larsson N.G., Clayton D.A. Molecular genetic aspects of human mitochondrial disorders. Annu Rev Genet 1995, 29:151-178.
28. von Kleist-Retzow J.C., Cormier-Daire V., Viot G., et al. Antenatal manifestations of mitochondrial respiratory chain deficiency. J Pediatr 2003, 143:208-212.
29. Cao L., Shitara H., Sugimoto M., et al. New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice. PLoS Genet 2009, 5. e1000756.
30. Fan W., Waymire K.G., Narula N., et al. A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations. Science 2008, 319:958-962.
31. Poulton J., Chiaratti M.R., Meirelles F.V., et al. Transmission of mitochondrial DNA diseases and ways to prevent them. PLoS Genet 2010, 6.
32. Feinberg A.P. Phenotypic plasticity and the epigenetics of human disease. Nature 2007, 447:433-440.
33. Wallace D.C., Fan W. Energetics, epigenetics, mitochondrial genetics. Mitochondrion 2010, 10:12-31.
34. McArdle H.J., Andersen H.S., Jones H., et al. Fetal programming: causes and consequences as revealed by studies of dietary manipulation in rats - a review. Placenta 2006, 27(Suppl. A):S56-S60.
35. Wallace D.C. Mitochondria, bioenergetics, and the epigenome in eukaryotic and human evolution. Cold Spring Harbor Symp Quant Biol 2009, 74:383-393.
36. Fuchs S.M., Laribee R.N., Strahl B.D. Protein modifications in transcription elongation. Biochim Biophys Acta 2009, 1789:26-36.
37. Yu J., Auwerx J. The role of sirtuins in the control of metabolic homeostasis. Ann NY Acad Sci 2009, 1173(Suppl. 1):E10-E19.
38. Cervera A.M., Bayley J.P., Devilee P., et al. Inhibition of succinate dehydrogenase dysregulates histone modification in mammalian cells. Molec Cancer 2009, 8:89.
39. Poon H.K., Lee K.H., Wong C.L., et al. Absence of paternal accessory sex gland secretions disturbs epigenetic reprogramming and expression of Igf2 and Dlk1 in golden hamster embryos. Theriogenology 2009, 71:1367-1380.
40. Assou S., Boumela I., Haouzi D., et al. Dynamic changes in gene expression during human early embryo development: from fundamental aspects to clinical applications. Hum Reprod Update 2011, 17:272-290.
41. Houghton F.D., Leese H.J. Metabolism and developmental competence of the preimplantation embryo. Eur J Obstet Gynecol Reprod Biol 2004, 115(Suppl. 1):S92-S96.
42. Van Blerkom J., Davis P.W., Lee J. ATP content of human oocytes and developmental potential and outcome after in-vitro fertilization and embryo transfer. Hum Reprod 1995, 10:415-424.
43. Nissenkorn A., Michelson M., Ben-Zeev B., et al. Inborn errors of metabolism: a cause of abnormal brain development. Neurology 2001, 56:1265-1272.
44. Rotig A., de Lonlay P., Chretien D., et al. Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia. Nat Genet 1997, 17:215-217.
45. Harding A.E. Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features. Brain 1981, 104:589-620.
46. Yu-Wai-Man P., Griffiths P.G., Hudson G., et al. Inherited mitochondrial optic neuropathies. J Med Genet 2009, 46:145-158.
47. Peixoto P.M., Ryu S.Y., Pruzansky D.P., et al. Mitochondrial apoptosis is amplified through gap junctions. Biochem Biophys Res Commun 2009, 390:38-43.
48. Dassa E.P., Dufour E., Goncalves S., et al. Expressing the alternative oxidase complements cytochrome c oxidase deficiency in human cells. EMBO Molec Med 2009, 1:30-36.
49. Shao J., White C.C., Dabrowski M.J., et al. The role of mitochondrial and oxidative injury in BDE 47 toxicity to human fetal liver hematopoietic stem cells. Toxicol Sci 2008, 101:81-90.
50. Wang Y.Y., Sui K.X., Li H., et al. The effects of lead exposure on placental NF-kappaB expression and the consequences for gestation. Reprod Toxicol 2009, 27:190-195.
51. Marx J., Pretorius E., Bornman M.S. The neurotoxic effects of prenatal cardiac glycoside exposure: a hypothesis. Neurotoxicol Teratol 2006, 28:135-143.
52. Henderson G.I., Chen J.J., Schenker S. Ethanol, oxidative stress, reactive aldehydes, and the fetus. Front Biosci 1999, 4:D541-D550.
53. Blanche S., Tardieu M., Rustin P., et al. Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues. Lancet 1999, 354:1084-1089.
54. Martin F., Taylor G.P. The safety of highly active antiretroviral therapy for the HIV-positive pregnant mother and her baby: is 'the more the merrier'?. J Antimicrob Chemother 2009, 64:895-900.
55. Power J.D., Fair D.A., Schlaggar B.L., et al. The development of human functional brain networks. Neuron 2010, 67:735-748.
56. Schofield P.N., Gkoutos G.V., Gruenberger M., et al. Phenotype ontologies for mouse and man: bridging the semantic gap. Dis Model Mech 2010, 3:281-289.
57. Bezek S., Ujhazy E., Dubovicky M., et al. Nongenomic memory of foetal history in chronic diseases development. Neuroendocrinol Lett 2008, 29:620-626.