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Keywords: HDAC6
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Journal Articles
In collection:
Cytoskeleton
J Cell Sci (2020) 133 (11): jcs242842.
Published: 11 June 2020
... polymerisation following GC treatment, identifying cytoskeletal stabilisation as the likely mechanism of action. HDAC6 overexpression, but not knockdown of αTAT1, rescued the GC effect, implicating HDAC6 as the GR effector. Consistent with this hypothesis, ligand-dependent cytoplasmic interaction between GR...
Includes: Supplementary data
Journal Articles
J Cell Sci (2019) 132 (6): jcs226506.
Published: 26 March 2019
... that acetylated tubulin significantly decreases upon perturbation of the Arp2/3-branched actin. We subsequently discover that HDAC6 participates in this process by altering its interaction with tubulin and the Arp2/3-stabilizer cortactin. We further identify that the homeostasis of branched actin controls...
Includes: Supplementary data
Journal Articles
In collection:
Cytoskeleton
J Cell Sci (2016) 129 (15): 2972–2982.
Published: 01 August 2016
...Renate Hvidsten Skoge; Mathias Ziegler ABSTRACT Deacetylation of α-tubulin at lysine 40 is catalyzed by two enzymes, the NAD-dependent deacetylase SIRT2 and the NAD-independent deacetylase HDAC6, in apparently redundant reactions. In the present study, we tested whether these two enzymes might have...
Journal Articles
J Cell Sci (2014) 127 (22): 4954–4963.
Published: 15 November 2014
..., but also elevates the risk of mitochondrial oxidative damage. Here, we present evidence that metabolically challenged mitochondria undergo active fusion to suppress oxidative stress. In response to glucose starvation, mitofusin 1 (MFN1) becomes associated with the protein deacetylase HDAC6...
Includes: Supplementary data
Journal Articles
J Cell Sci (2014) 127 (18): 4052–4063.
Published: 15 September 2014
... in these pathways is still being elucidated. Here, we show that the scaffolding protein SQSTM1 directly interacts with dynein through a previously unidentified dynein-binding site. This interaction is independent of HDAC6, a known interacting protein of both SQSTM1 and dynein. However, knockdown of HDAC6 increases...
Journal Articles
J Cell Sci (2011) 124 (16): 2692–2701.
Published: 15 August 2011
... A or tubacin, inhibitors of histone deacetylase (HDAC), indicating that the non-ubiquitylated aggregates of STAT5A_ΔE18 were sequestered into aggresomes in an HDAC6-dependent manner. Moreover, p62 was bound to STAT5A_ΔE18 through its PB1 domain, and the oligomerization of p62 was required for this interaction...
Includes: Supplementary data
Journal Articles
J Cell Sci (2009) 122 (13): 2274–2282.
Published: 01 July 2009
...) or PEST-truncated Nek3 leads to distorted neuronal morphology with disturbed polarity and deacetylation of microtubules via HDAC6 in its kinase-dependent manner. Thus, the phosphorylation at Thr475 serves as a regulatory switch that alters Nek3 function. The deacetylation of microtubules in neurons...
Includes: Supplementary data
Journal Articles
J Cell Sci (2007) 120 (8): 1469–1479.
Published: 15 April 2007
... deacetylase 6 (HDAC6) induces a parallel alteration in cell migration. Using tubacin to block deacetylation of α-tubulin, and not other HDAC6 substrates, yielded a motility reduction equivalent to agents that block all NAD-independent HDACs. Accordingly, we investigated how the failure to deacetylate tubulin...
Includes: Multimedia, Supplementary data
Journal Articles
J Cell Sci (2005) 118 (13): 2901–2911.
Published: 01 July 2005
... with the recently identified microtubule deacetylase HDAC6 but that it also activated the microtubule deacetylase activity of HDAC6 in an in vitro deacetylase assay. Finally, we found that during osteoclastogenesis, there is a correlation between the increase in microtubule acetylation and the podosome belt...