Association of mitochondrial DNA deletions and cochlear pathology: A molecular biologic tool

Laryngoscope

Volumn 106, Issue 6, 1996, Pages 777-783

  Seidman, Michael D ^a   Bai, Uma ^a   Khan, Mumtaz J ^a   Murphy, Michael P ^a   Quirk, Wayne S ^b   Castora, Frank J ^c   Hinojosa, Raul ^d  

^a HENRY FORD HOSPITAL   (United States)

^b WAYNE STATE UNIVERSITY   (United States)

^c EASTERN VIRGINIA MEDICAL SCHOOL   (United States)

^d UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ANIMAL TISSUE; ARTICLE; BASE PAIRING; DNA DETERMINATION; GENE DELETION; HEARING LOSS; HUMAN; HUMAN TISSUE; NONHUMAN; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRESBYACUSIS; PRIORITY JOURNAL; RAT; SEQUENCE ANALYSIS;

AGED; ANIMALS; BASE SEQUENCE; CHROMOSOME DELETION; COCHLEAR DISEASES; DNA PRIMERS; DNA, MITOCHONDRIAL; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; PRESBYCUSIS; RATS; STRIA VASCULARIS; TEMPORAL MUSCLE; VESTIBULOCOCHLEAR NERVE;

EID: 0029945725     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-199606000-00021     Document Type: Article

References (44)

1. Schapira AH, Cooper JM, Dexter D, et al. Mitochondrial complex I deficiency in Parkinson's disease. Lancet. 1989;1: (8649):1269.
2. Miyabayashi S, Hanamizu H, Endo H, et al. A new type of mitochondrial DNA deletion in patients with encephalomyopathy. J Inherit Metab Dis. 1991;14:805-812.
3. Ballinger SW, Shoffner JM, Hedaya EV, et al. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion. Nat Genet. 1992;1:3-7.
4. Corral-Debrinski M, Sapien G, Shoffner JM, et al. Hypoxemia is associated with mitochondrial DNA damage and gene induction. JAMA. 1991;266:1812-1816.
5. Shoffner JM, Wallace DC. Mitochondrial genetics: principles and practice. Am J Human Genet. 1992;51:1179-1186.
6. Cortopassi GA, Arnheim M. Detection of a specific mitochondrial DNA deletion in tissues of older humans. Nucleic Acids Res. 1990;18:6927-6933.
7. Wallace DC. Mitochondrial genes and disease. Hosp Pract (Off Ed). 1986;21:77-87.
8. Wallace DC, Lott MT, Lezza AM, et al. Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction. Paediatr Res. 1990;28:525-528.
9. Yen TC, Chen YS, King KL, et al. Liver mitochondrial respiratory functions decline with age. Biochem Biophys Res Comm. 1989;165:944-1003.
10. Anderson S, Bankier AT, Barrel BG, et al. Sequence and organization of the human mitochondrial genome. Nature. 1981; 290:457-465.
11. Linnane AW, Marzuki S, Ozawa T, et al. Mitochondrial DNA mutations as an important contributor to ageing and degenerative disease. Lancet. 1985;1(8639):642-645.
12. Wallace DC. Mitochondrial genes and disease. Hosp Pract. 1986;21:77-92.
13. Wallace DC. Mitochondrial DNA mutations and neuromuscular disease. Trends Genet. 1989;5:9-13.
14. Wallace DC. Mitochondrial genetics: a paradigm for ageing and degenerative diseases? Science. 1992;256:628-632.
15. Giles RE, Blanc H, Cann HM, et al. Maternal inheritance of mitochondrial DNA. Proc Natl Acad Sci U S A. 1980;77:6715-6719.
16. Case JT, Wallace DC. Maternal inheritance of mitochondrial DNA polymorphism in cultured human fibroblasts. Somat Cell Genet. 1981;7:103-108.
17. Shoffner JM, Lott MT, Voljavec AS, et al. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip replication model and metabolic therapy. Proc Natl Acad Sci U S A. 1989;86:7952-7956.
18. Grossman LI. Mitochondrial DNA in sickness and in health. Am J Hum Genet. 1990;46:415-417.
19. DiMauro S, Bonilla E, Lombes A, et al. Mitochondrial encephalomyopathies. Neurol Clin. 1990;8:483-506.
20. Pavlakis SG, Phillips PC, DiMauro S, et al. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: a distinctive clinical syndrome. Ann Neurol. 1984; 16:481-488.
21. Seibel P, Degoul F, Romero N, et al. Identification of point mutations by mispairing PCR as exemplified by MERRF disease. Biochem Biophys Res Comm. 1990;173:561-565.
22. Shoffner JM, Lott MT, Lezza AM, et al. Myoclonic epilepsy and ragged-red fiber disease is associated with a mitochondrial DNA tRNA (Lys) mutation. Cell. 1990;61:931-937.
23. Piper HM, Sezer O, Schleyer M, et al. Development of ischemia induced damage in defined mitochondrial subpopulations. J Mol Cell Cardiol. 1985;17:885-896.
24. Gold M, Rapin I, Shanske S. Mitochondrial inheritance of acquired deafness. Ann N Y Acad Sci. 1991;301-302.
25. Prezant TR, Fischel-Ghodsian N, Bu X, et al. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Am J Otolaryngol. 1993;14630:399-403.
26. Wackym PA, Simpson TA, Gantz BJ. Polymerase chain reaction amplification of DNA from archival celloidin-embedded human temporal bone sections. LARYNGOSCOPE. 1993;103: 583-588.
27. Simpson TA, Smith RJH. Amplification of mitochondrial DNA from archival temporal bone specimens. LARYNGOSCOPE. 1995;105:28-34.
28. Maniatis T, Sambrook J, Fritsch EF. Molecular Cloning: A Laboratory Manual. 2nd ed. Cold Spring Harbor: Cold Spring Harbor Laboratory; 1989.
29. Gates GA, Caspery DM, Clark W, et al. Presbyacusis. Otolaryngol Head Neck Surg. 1986;100:266-271.
30. Bjorksten J. Theoretical Aspects of Ageing. New York: New York Academic Press; 1974.
31. Leibovitz BE, Siegl BV. Aspects of free radical reactions in biological systems: ageing. J Gerontol. 1980;35:45-56.
32. Shoffner JM, Wallace DC. Heart disease a mitochondrial DNA mutations. Heart Dis Stroke. 1992;1:235-41.
33. Hattori K, Tanaka M, Sugiyama S, et al. Age-dependent increase in deleted mitochondrial DNA in the human heart: possible contributory factor to presbycardia. Am Heart J. 1991;121:1735-1742.
34. Ames BN. Dietary carcinogens and anticarcinogens. Oxygen radicals and degenerative diseases. Science. 1983;221:1256-1264.
35. Trounce I, Byrne E, Marzuki S. Decline in skeletal muscle mitochondrial respiratory chain function: possible factor in ageing (see Comments). Lancet. 1989;1(8639):637-639.
36. Richter C, Park JW, Ames BN. Normal oxidative damage to mitochondrial DNA and nuclear DNA is extensive. Proc Natl Acad Sci U S A. 1988;85:6465-6467.
37. Nohl H, Hegner D. Do mitochondria produce oxygen radicals in vivo? Eur J Biochem. 1978;82:563-567.
38. Piko L, Houghman AJ, Bulpitt KJ. Studies of sequence heterogeneity of mitochondrial DNA from rat and mouse tissue: evidence of an increased frequency of deletions/additions with ageing. Mech Ageing Dev. 1988;43:279-293.
39. Muller-Hocker J. Cytochrome-c oxidase deficient cardiomyocytes in the human heart: an age related phenomenon. A histochemical cytochemical study. Am J Pathol. 1989;134: 1167-1173.
40. Bandy B, Davison AJ. Mitochondrial mutations may increase oxidative stress: implications for carcinogenesis and aging? Free Radic Biol Med. 1990;8:523-539.
41. Kerner MM, Wackym PA, Popper P, et al. Cloning and sequencing of genomic DNA extracted from archival human temporal bone sections. LARYNGOSCOPE. 1994;104:127-134.
42. Burgess RC, Michaels L, Bale JF Jr, et al. Polymerase chain reaction amplification of herpes simplex viral DNA from the geniculate ganglion of a patient with Bell's palsy. Ann Otol Rhinol Laryngol. 1994;103;775-779.
43. Manaligod J, Fischel-Ghodsian N, Keithley EM, et al. Molecular analysis of archival temporal bone tissues. Presentation to the Meeting of the Association for Research in Otolaryngology. St. Petersburg, Fla., Feb. 1996.
44. McKenna MJ, Kristiansen AJ, Haines JL. Reverse transcription - polymerase chain reaction (RT-PCR) for the demonstration of RNA sequences in archival human temporal bones. Presentation to the Meeting of the Association for Research in Otolaryngology. St. Petersburg, Fla., Feb. 1996.