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  1. 原著論文

Aging-dependent large accumulation of muscle-specific point mutations in the transcription/replication control region of human mitochondrial DNA

https://repo.qst.go.jp/records/45400
https://repo.qst.go.jp/records/45400
33511e80-7a7e-4a57-8598-561895c76519
Item type 学術雑誌論文 / Journal Article(1)
公開日 2009-01-15
タイトル
タイトル Aging-dependent large accumulation of muscle-specific point mutations in the transcription/replication control region of human mitochondrial DNA
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Michikawa, Yuichi

× Michikawa, Yuichi

WEKO 450979

Michikawa, Yuichi

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道川 祐市

× 道川 祐市

WEKO 450980

en 道川 祐市

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内容記述タイプ Abstract
内容記述 The aging-dependent large accumulation of specific point mutations, especially the most frequent mutation T414G, in the cultured human skin fibroblast mtDNA transcription/replication regulatory region raised the question of their occurrence in post-mitotic tissues. In the present work, analysis of biopsied or autopsied human skeletal muscle from variously aged individuals revealed the absence or only minimal presence of those skin fibroblast mutations. By contrast, surprisingly, most of 26 individuals 53 to 92 years old, without a known history of neuromuscular disease, exhibited at the same region of human mtDNA in muscle an accumulation of two new point mutations, i.e., A189G and T408A, which were absent or marginally present in the muscle of 19 individuals younger than 34 years. These two mutations were not found in the skin fibroblasts from 22 subjects 64 to 101 years of age (T408A), or were present only in three subjects in very low amounts (A189G). Furthermore, in several older individuals exhibiting an accumulation in muscle of one or both of these mutations, they were nearly absent in other post-mitotic tissues, whereas the most frequent fibroblast-specific mutation (T414G) was present in skin autopsy, but not in muscle. The striking tissue specificity of the aging-dependent mtDNA point mutations and their mapping at critical sites for mtDNA transcription/replication strongly point to the involvement of a specific mutagenic machinery or a specific advantage for the mtDNA replication/transmission and to the functional relevance of these mutations during human aging processes.
書誌情報 Advances in Exercise and Sports Physiology

巻 14, 号 3, p. 53-56, 発行日 2008-12
ISSN
収録物識別子タイプ ISSN
収録物識別子 1340-3141
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