کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2047828 | 1074036 | 2012 | 5 صفحه PDF | دانلود رایگان |

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.
► HDAC6 expression correlates with mitochondrial metabolic activity.
► HDAC6 regulates mitochondrial metabolic activity in the cytoplasm.
► Both deacetylase and ubiquitin binding activities of HDAC6 are linked to it.
► HDAC6 does not affect the expression of nuclear-encoded mitochondrial enzymes.
► Hsp90 partly mediates the regulation of mitochondrial metabolic activity by HDAC6.
Journal: FEBS Letters - Volume 586, Issue 9, 7 May 2012, Pages 1379–1383