| Literature DB >> 28283581 |
Tomoko Satake1, Kazunari Yamashita2, Kenji Hayashi2, Satoko Miyatake3, Miwa Tamura-Nakano4, Hiroshi Doi5, Yasuhide Furuta6,7, Go Shioi7, Eriko Miura8, Yukari H Takeo8, Kunihiro Yoshida9, Hiroyuki Yahikozawa10, Naomichi Matsumoto3, Michisuke Yuzaki8, Atsushi Suzuki11.
Abstract
The axon initial segment (AIS) is a specialized domain essential for neuronal function, the formation of which begins with localization of an ankyrin-G (AnkG) scaffold. However, the mechanism directing and maintaining AnkG localization is largely unknown. In this study, we demonstrate that in vivo knockdown of microtubule cross-linking factor 1 (MTCL1) in cerebellar Purkinje cells causes loss of axonal polarity coupled with AnkG mislocalization. MTCL1 lacking MT-stabilizing activity failed to restore these defects, and stable MT bundles spanning the AIS were disorganized in knockdown cells. Interestingly, during early postnatal development, colocalization of MTCL1 with these stable MT bundles was observed prominently in the axon hillock and proximal axon. These results indicate that MTCL1-mediated formation of stable MT bundles is crucial for maintenance of AnkG localization. We also demonstrate that Mtcl1 gene disruption results in abnormal motor coordination with Purkinje cell degeneration, and provide evidence suggesting possible involvement of MTCL1 dysfunction in the pathogenesis of spinocerebellar ataxia.Entities:
Keywords: Purkinje cells; axon initial segment; microtubule cross‐linking factor 1; microtubules
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Year: 2017 PMID: 28283581 PMCID: PMC5412768 DOI: 10.15252/embj.201695630
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598