Publication Date:
1989-04-21
Description:
Kearns-Sayre syndrome (KSS) and progressive external ophthalmoplegia (PEO) are related neuromuscular disorders characterized by ocular myopathy and ophthalmoplegia. Almost all patients with KSS and about half with PEO harbor large deletions in their mitochondrial genomes. The deletions differ in both size and location, except for one, 5 kilobases long, that is found in more than one-third of all patients examined. This common deletion was found to be flanked by a perfect 13-base pair direct repeat in the normal mitochondrial genome. This result suggests that homologous recombination deleting large regions of intervening mitochondrial DNA, which previously had been observed only in lower eukaryotes and plants, operates in mammalian mitochondrial genomes as well, and is at least one cause of the deletions found in these two related mitochondrial myopathies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schon, E A -- Rizzuto, R -- Moraes, C T -- Nakase, H -- Zeviani, M -- DiMauro, S -- NS11766/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1989 Apr 21;244(4902):346-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurology, Columbia University, New York, NY 10032.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2711184" target="_blank"〉PubMed〈/a〉
Keywords:
Base Composition
;
Base Sequence
;
Chromosome Deletion
;
DNA, Mitochondrial/*genetics
;
Gene Amplification
;
Humans
;
Kearns-Sayre Syndrome/*genetics
;
Molecular Sequence Data
;
Ophthalmoplegia/*genetics
;
RNA, Messenger/genetics
;
Recombination, Genetic
;
Repetitive Sequences, Nucleic Acid
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
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