New patterns of inheritance in mitochondrial disease.

With the identification of a patient with mutated mitochondrial DNA (mtDNA) of paternal origin, it has been unequivocally proven that not only does paternal mtDNA survive in the zygote, but it can also contribute substantially to the mtDNA pool of adult, human skeletal muscle. The questions are: how often does paternal mtDNA inheritance occur and what mechanisms are involved? In this paper, we will review current knowledge on the fate of sperm mitochondria after fertilization and discuss the impact paternal inheritance may have on our understanding of mitochondrial biology.

[1]  A. Wilson,et al.  Paternal inheritance of mitochondrial DNA in mice , 1991, Nature.

[2]  M. Stoneking,et al.  Mitochondrial mutation rate revisited: hot spots and polymorphism , 1998, Nature Genetics.

[3]  M. Stoneking,et al.  Mitochondrial DNA and human evolution , 1987, Nature.

[4]  G. Schatten,et al.  Ubiquitinated Sperm Mitochondria, Selective Proteolysis, and the Regulation of Mitochondrial Inheritance in Mammalian Embryos1 , 2000, Biology of reproduction.

[5]  A. Eyre-Walker,et al.  Mitochondrial Steve: paternal inheritance of mitochondria in humans , 2003 .

[6]  V. Salas,et al.  A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria , 1996, Nature Genetics.

[7]  L. Kvist,et al.  Paternal leakage of mitochondrial DNA in the great tit (Parus major). , 2003, Molecular biology and evolution.

[8]  P. Sutovsky,et al.  Ubiquitination of Prohibitin in Mammalian Sperm Mitochondria: Possible Roles in the Regulation of Mitochondrial Inheritance and Sperm Quality Control1 , 2003, Biology of reproduction.

[9]  S. Dimauro,et al.  A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria , 1999, Annals of neurology.

[10]  B. N. Day,et al.  Early Degradation of Paternal Mitochondria in Domestic Pig (Sus scrofa) Is Prevented by Selective Proteasomal Inhibitors Lactacystin and MG1321 , 2003, Biology of reproduction.

[11]  A. Eyre-Walker,et al.  Do mitochondria recombine in humans? , 2000, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[12]  Elimination of paternal mitochondrial DNA in intraspecific crosses during early mouse embryogenesis. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Yau-Huei Wei,et al.  Oxidative Stress and Mitochondrial DNA Mutations in Human Aging , 1998, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[14]  H. Cann,et al.  Maternal inheritance of human mitochondrial DNA. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[15]  D. Turnbull,et al.  Analysis of European mtDNAs for recombination. , 2001, American journal of human genetics.

[16]  F. Sanger,et al.  Sequence and organization of the human mitochondrial genome , 1981, Nature.

[17]  B. Milligan Is organelle DNA strictly maternally inherited? Power analysis of a binomial distribution , 1992 .

[18]  S. Dimauro,et al.  Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA. , 1999, The New England journal of medicine.

[19]  C. Cazeneuve,et al.  Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection. , 1999, American journal of human genetics.

[20]  A. Hall,et al.  Mismatch repair activity in mammalian mitochondria. , 2003, Nucleic acids research.

[21]  P. Awadalla,et al.  Does Human mtDNA Recombine? , 2001, Journal of Molecular Evolution.

[22]  P. Donnelly,et al.  The mutation rate in the human mtDNA control region. , 2000, American journal of human genetics.

[23]  C. Birky Uniparental inheritance of mitochondrial and chloroplast genes: mechanisms and evolution. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[24]  M. Schwartz,et al.  Paternal inheritance of mitochondrial DNA. , 2002, The New England journal of medicine.

[25]  A. Eyre-Walker,et al.  How clonal are human mitochondria? , 1999, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[26]  A. Ciechanover,et al.  The ubiquitin system. , 1998, Annual review of biochemistry.

[27]  J. Cummins,et al.  Misconceptions about mitochondria and mammalian fertilization: implications for theories on human evolution. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[28]  The inheritance of genes in mitochondria and chloroplasts: laws, mechanisms, and models. , 2001 .

[29]  S. Dimauro,et al.  Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA , 2000, Neurology.

[30]  H. Yonekawa,et al.  Maternal inheritance of mouse mtDNA in interspecific hybrids: segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakage. , 1998, Genetics.

[31]  J. Cummins Mitochondrial DNA in mammalian reproduction. , 1998, Reviews of reproduction.

[32]  H. Jacobs,et al.  Behaviour of a population of partially duplicated mitochondrial DNA molecules in cell culture: segregation, maintenance and recombination dependent upon nuclear background. , 1997, Human molecular genetics.

[33]  H. Yonekawa,et al.  Selective and continuous elimination of mitochondria microinjected into mouse eggs from spermatids, but not from liver cells, occurs throughout embryogenesis. , 2000, Genetics.

[34]  S. Pääbo,et al.  Mitochondrial genome variation and the origin of modern humans , 2000, Nature.

[35]  D. Bozon,et al.  A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance. , 1996, Molecular and cellular probes.

[36]  James B. Anderson,et al.  mtDNA recombination in a natural population. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[37]  E. Ruiz-Pesini,et al.  Mitochondrial DNA Content of Human Spermatozoa1 , 2003, Biology of reproduction.

[38]  P. Awadalla,et al.  Linkage disequilibrium and recombination in hominid mitochondrial DNA. , 1999, Science.

[39]  R. Rosenberg The Molecular and Genetic Basis of Neurological Disease , 1997 .

[40]  B. Thyagarajan,et al.  Mammalian Mitochondria Possess Homologous DNA Recombination Activity* , 1996, The Journal of Biological Chemistry.

[41]  C. Jonge,et al.  Failure of elimination of paternal mitochondrial DNA in abnormal embryos , 2000, The Lancet.

[42]  P. Heckerling Paternal inheritance of mitochondrial DNA. , 2002 .

[43]  E. Hagelberg Recombination or mutation rate heterogeneity? Implications for Mitochondrial Eve. , 2003, Trends in genetics : TIG.

[44]  H. Jacobs,et al.  No sex please, we're mitochondria: a hypothesis on the somatic unit of inheritance of mammalian mtDNA. , 2000, BioEssays : news and reviews in molecular, cellular and developmental biology.

[45]  P Barrière,et al.  Mitochondrial DNA content affects the fertilizability of human oocytes. , 2001, Molecular human reproduction.

[46]  G. Schatten,et al.  Development: Ubiquitin tag for sperm mitochondria , 1999, Nature.