QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

HOME  |   SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article Full Text Full Text (PDF) Submit an eLetter Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via ISI Web of Science (24) Citing Articles via Google Scholar Google Scholar Articles by Zhou, L. Articles by Miller, C. A. Search for Related Content PubMed PubMed Citation Articles by Zhou, L. Articles by Miller, C. A.

 Previous Article  |  Next Article 

Volume 17, Number 20, Issue of October 15, 1997 pp. 7746-7753
Copyright ©1997 Society for Neuroscience

Myoclonic Epilepsy and Ragged Red Fibers (MERRF) Syndrome: Selective Vulnerability of CNS Neurons Does Not Correlate with the Level of Mitochondrial tRNA^lys Mutation in Individual Neuronal Isolates

Received Feb. 27, 1997; revised July 15, 1997; accepted July 30, 1997.

Li Zhou¹, Anne Chomyn², Giuseppe Attardi², and Carol A. Miller¹

¹ Departments of Pathology and Neurology, University of Southern California School of Medicine, Los Angeles, California 90033, and ² Division of Biology, California Institute of Technology, Pasadena, California 91125

Selective vulnerability of subpopulations of neurons is a striking feature of neurodegeneration. Mitochondrially transmitted diseases are no exception. In this study CNS tissues from a patient with myoclonus epilepsy and ragged red fibers (MERRF) syndrome, which results from an A to G transition of nucleotide (nt) 8344 in the mitochondrial tRNA^Lys gene, were examined for the proportion of mutant mtDNA. Either individual neuronal somas or the adjacent neuropil and glia were microdissected from cryostat tissue sections of histologically severely affected brain regions, including dentate nuclei, Purkinje cells, and inferior olivary nuclei, and from a presumably less affected neuronal subpopulation, the anterior horn cells of the spinal cord. Mutant and normal mtDNA were quantified after PCR amplification with a mismatched primer and restriction enzyme digestion. Neurons and the surrounding neuropil and glia from all CNS regions that were analyzed exhibited high proportions of mutant mtDNA, ranging from 97.6 ± 0.7% in Purkinje cells to 80.6 ± 2.8% in the anterior horn cells. Within each neuronal group that was analyzed, neuronal soma values were similar to those in the surrounding neuropil and glia or in the regional tissue homogenate. Surprisingly, as compared with controls, neuronal loss ranged from 7% of the Purkinje cells to 46% of the neurons of the dentate nucleus in MERRF cerebellum. Thus, factors other than the high proportion of mutant mtDNA, in particular nuclear-controlled neuronal differences among various regions of the CNS, seem to contribute to the mitochondrial dysfunction and ultimate cell death.

Key words: MERRF syndrome; CNS microdissection; PCR; neurodegeneration; tRNA^Lys; mtDNA

This article has been cited by other articles:

				L. Jacobs, M. Gerards, P. Chinnery, J. Dumoulin, I. de Coo, J. Geraedts, and H. Smeets mtDNA point mutations are present at various levels of heteroplasmy in human oocytes Mol. Hum. Reprod., March 1, 2007; 13(3): 149 - 154*. [Abstract] [Full Text] [PDF]

				S. Winterthun, G. Ferrari, L. He, R. W. Taylor, M. Zeviani, D. M. Turnbull, B. A. Engelsen, G. Moen, and L. A. Bindoff Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase {gamma} mutations Neurology, April 12, 2005; 64(7): 1204 - 1208. [Abstract] [Full Text] [PDF]

				D. Prayer, N. Grois, H. Prosch, H. Gadner, and A. J. Barkovich MR Imaging Presentation of Intracranial Disease Associated with Langerhans Cell Histiocytosis AJNR Am. J. Neuroradiol., May 1, 2004; 25(5): 880 - 891. [Abstract] [Full Text] [PDF]

				J. Uusimaa, S. Finnila, L. Vainionpaa, M. Karppa, R. Herva, H. Rantala, I. E. Hassinen, and K. Majamaa A Mutation in Mitochondrial DNA-Encoded Cytochrome c Oxidase II Gene in a Child With Alpers-Huttenlocher-Like Disease Pediatrics, March 1, 2003; 111(3): e262 - 268. [Abstract] [Full Text] [PDF]

				L. He, P. F. Chinnery, S. E. Durham, E. L. Blakely, T. M. Wardell, G. M. Borthwick, R. W. Taylor, and D. M. Turnbull Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR Nucleic Acids Res., July 15, 2002; 30(14): e68 - e68. [Abstract] [Full Text] [PDF]

				R. W. Taylor, G. A. Taylor, S. E. Durham, and D. M. Turnbull The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations Nucleic Acids Res., August 1, 2001; 29(15): e74 - e74. [Abstract] [Full Text] [PDF]

				G. Silvestri, T. Mongini, F. Odoardi, A. Modoni, G. deRosa, C. Doriguzzi, L. Palmucci, P. Tonali, and S. Servidei A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency Neurology, April 25, 2000; 54(8): 1693 - 1696. [Abstract] [Full Text] [PDF]

				R. Rossignol, M. Malgat, J.-P. Mazat, and T. Letellier Threshold Effect and Tissue Specificity. IMPLICATION FOR MITOCHONDRIAL CYTOPATHIES J. Biol. Chem., November 19, 1999; 274(47): 33426 - 33432. [Abstract] [Full Text] [PDF]

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help