HDAC6 a new cellular stress surveillance factor

P Matthias, M Yoshida, S Khochbin - Cell cycle, 2008 - Taylor & Francis
Cell cycle, 2008Taylor & Francis
Less than a decade has passed since HDAC6 was first identified and regarded as an
unusual histone deacetylase harbouring two catalytic domains. Early demonstration of its
cytoplasmic localisation, its ubiquitin-binding and its tubulin-deacetylase activities took
HDAC6 far away from everything known to involve other histone-deacetylases. Recent
discoveries confirmed the very unique functions of HDAC6 among deacetylases and pointed
to this protein as a master regulator of cell response to cytotoxic assaults. HDAC6 appears …
Less than a decade has passed since HDAC6 was first identified and regarded as an unusual histone deacetylase harbouring two catalytic domains. Early demonstration of its cytoplasmic localisation, its ubiquitin-binding and its tubulin-deacetylase activities took HDAC6 far away from everything known to involve other histone-deacetylases. Recent discoveries confirmed the very unique functions of HDAC6 among deacetylases and pointed to this protein as a master regulator of cell response to cytotoxic assaults. HDAC6 appears both as a sensor of stressful stimuli and as an effector, which, thanks to its wide range of activities, mediates and coordinates appropriate cell responses.
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