Abstract
Nuclear DNA is tightly packed into nucleosomal structure. In con-trast, human mitochondrial DNA (mtDNA) had long been believed to be rather naked because mitochondria lack histone. Mitochondrial transcription factor A (TFAM), a member of a high mobility group (HMG) protein family and a first-identified mitochondrial transcription factor, is essential for maintenance of mitochondrial DNA. Abf2, a yeast counterpart of human TFAM, is abun-dant enough to cover the whole region of mtDNA and to play a histone-like role in mitochondria. Human TFAM is indeed as abundant as Abf2, suggesting that TFAM also has a histone-like architectural role for maintenance of mtDNA. When human mitochondria are solubilized with non-ionic detergent Nonidet-P40 and then separated into soluble and particulate fractions, most TFAM is recovered from the particulate fraction together with mtDNA, suggesting that human mtDNA forms a nucleoid structure. TFAM is tightly associated with mtDNA as a main component of the nucleoid.
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© 2004 Springer-Verlag Berlin Heidelberg
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Kanki, T. et al. (2004). Mitochondrial Nucleoid and Transcription Factor A. In: Lee, H.K., DiMauro, S., Tanaka, M., Wei, YH. (eds) Mitochondrial Pathogenesis. Annals of the New York Academy of Sciences, vol 1011. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-41088-2_7
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DOI: https://doi.org/10.1007/978-3-662-41088-2_7
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