Septins promote dendrite and axon development by negatively regulating microtubule stability via HDAC6-mediated deacetylation

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Septins promote dendrite and axon development by negatively regulating microtubule stability via HDAC6-mediated deacetylation

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Title: Septins promote dendrite and axon development by negatively regulating microtubule stability via HDAC6-mediated deacetylation
Author: Ageta-Ishihara, Natsumi; Miyata, Takaki; Ohshima, Chika; Watanabe, Masahiko; Sato, Yoshikatsu; Hamamura, Yuki; Higashiyama, Tetsuya; Mazitschek, Ralph; Bito, Haruhiko; Kinoshita, Makoto

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Citation: Ageta-Ishihara, Natsumi, Takaki Miyata, Chika Ohshima, Masahiko Watanabe, Yoshikatsu Sato, Yuki Hamamura, Tetsuya Higashiyama, Ralph Mazitschek, Haruhiko Bito, and Makoto Kinoshita. 2013. “Septins promote dendrite and axon development by negatively regulating microtubule stability via HDAC6-mediated deacetylation.” Nature Communications 4 (1): 2532. doi:10.1038/ncomms3532. http://dx.doi.org/10.1038/ncomms3532.
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Abstract: Neurite growth requires two guanine nucleotide-binding protein polymers of tubulins and septins. However, whether and how those cytoskeletal systems are coordinated was unknown. Here we show that the acute knockdown or knockout of the pivotal septin subunit SEPT7 from cerebrocortical neurons impairs their interhemispheric and cerebrospinal axon projections and dendritogenesis in perinatal mice, when the microtubules are severely hyperacetylated. The resulting hyperstabilization and growth retardation of microtubules are demonstrated in vitro. The phenotypic similarity between SEPT7 depletion and the pharmacological inhibition of α-tubulin deacetylase HDAC6 reveals that HDAC6 requires SEPT7 not for its enzymatic activity, but to associate with acetylated α-tubulin. These and other findings indicate that septins provide a physical scaffold for HDAC6 to achieve efficient microtubule deacetylation, thereby negatively regulating microtubule stability to an optimal level for neuritogenesis. Our findings shed light on the mechanisms underlying the HDAC6-mediated coupling of the two ubiquitous cytoskeletal systems during neural development.
Published Version: doi:10.1038/ncomms3532
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826633/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11878988
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