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Depression of mitochondrial metabolism by downregulation of cytoplasmic deacetylase, HDAC6
Authors:Kamemura Kazuo  Ogawa Mitsutaka  Ohkubo Saki  Ohtsuka Yasuhiro  Shitara Yu  Komiya Tohru  Maeda Satoko  Ito Akihiro  Yoshida Minoru
Institution:Department of Bioscience, Nagahama Institute of Bio-Science and Technology, Nagahama, Shiga, Japan. k_kamemura@nagahama-i-bio.ac.jp
Abstract:Mitochondria perform multiple functions critical to the maintenance of cellular homeostasis. Here we report that the downregulation of histone deacetylase 6 (HDAC6) causes a reduction in the net activity of mitochondrial enzymes, including respiratory complex II and citrate synthase. HDAC6 deacetylase and ubiquitin-binding activities were both required for recovery of reduced mitochondrial metabolic activity due to the loss of HDAC6. Hsp90, a substrate of HDAC6, localizes to mitochondria and partly mediates the regulation of mitochondrial metabolic activity by HDAC6. Our finding suggests that HDAC6 regulates mitochondrial metabolism and might serve as a cellular homeostasis surveillance factor.
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