TY - JOUR
T1 - Elavl3 is essential for the maintenance of Purkinje neuron axons
AU - Ogawa, Yuki
AU - Kakumoto, Kyoko
AU - Yoshida, Tetsu
AU - Kuwako, Ken ichiro
AU - Miyazaki, Taisuke
AU - Yamaguchi, Junji
AU - Konno, Ayumu
AU - Hata, Junichi
AU - Uchiyama, Yasuo
AU - Hirai, Hirokazu
AU - Watanabe, Masahiko
AU - Darnell, Robert B.
AU - Okano, Hideyuki
AU - Okano, Hirotaka James
N1 - Funding Information:
This work was supported by a Grant-in-Aid of The Ishidsu Shun Memorial Scholarship and JSPS KAKENHI Grant Number 16J11920 to Yuki Ogawa, and JSPS KAKENHI Grant Number 17K09766, MEXT KAKENHI Grant Number 24111543, 26111723, and The Jikei University Strategic Prioritizing Research Fund to Hirotaka James Okano. We thank the following staff members for their contributions to this study: Minami Hasegawa and Chikako Hara-Miyauchi (The Jikei University School of Medicine) for valuable discussions, and Fumiko Ozawa (Keio University School of Medicine), Mariko Ito, Ayako M. Watabe, and Fusao Kato (The Jikei University School of Medicine) for technical assistance. We also would like to thank Nature Research Editing Service and Enago for the English language review.
Publisher Copyright:
© 2018, The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Neuronal Elav-like (nElavl or neuronal Hu) proteins are RNA-binding proteins that regulate RNA stability and alternative splicing, which are associated with axonal and synaptic structures. nElavl proteins promote the differentiation and maturation of neurons via their regulation of RNA. The functions of nElavl in mature neurons are not fully understood, although Elavl3 is highly expressed in the adult brain. Furthermore, possible associations between nElavl genes and several neurodegenerative diseases have been reported. We investigated the relationship between nElavl functions and neuronal degeneration using Elavl3−/− mice. Elavl3−/− mice exhibited slowly progressive motor deficits leading to severe cerebellar ataxia, and axons of Elavl3−/− Purkinje cells were swollen (spheroid formation), followed by the disruption of synaptic formation of axonal terminals. Deficit in axonal transport and abnormalities in neuronal polarity was observed in Elavl3−/− Purkinje cells. These results suggest that nElavl proteins are crucial for the maintenance of axonal homeostasis in mature neurons. Moreover, Elavl3−/− mice are unique animal models that constantly develop slowly progressive axonal degeneration. Therefore, studies of Elavl3−/− mice will provide new insight regarding axonal degenerative processes.
AB - Neuronal Elav-like (nElavl or neuronal Hu) proteins are RNA-binding proteins that regulate RNA stability and alternative splicing, which are associated with axonal and synaptic structures. nElavl proteins promote the differentiation and maturation of neurons via their regulation of RNA. The functions of nElavl in mature neurons are not fully understood, although Elavl3 is highly expressed in the adult brain. Furthermore, possible associations between nElavl genes and several neurodegenerative diseases have been reported. We investigated the relationship between nElavl functions and neuronal degeneration using Elavl3−/− mice. Elavl3−/− mice exhibited slowly progressive motor deficits leading to severe cerebellar ataxia, and axons of Elavl3−/− Purkinje cells were swollen (spheroid formation), followed by the disruption of synaptic formation of axonal terminals. Deficit in axonal transport and abnormalities in neuronal polarity was observed in Elavl3−/− Purkinje cells. These results suggest that nElavl proteins are crucial for the maintenance of axonal homeostasis in mature neurons. Moreover, Elavl3−/− mice are unique animal models that constantly develop slowly progressive axonal degeneration. Therefore, studies of Elavl3−/− mice will provide new insight regarding axonal degenerative processes.
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U2 - 10.1038/s41598-018-21130-5
DO - 10.1038/s41598-018-21130-5
M3 - Article
C2 - 29426875
AN - SCOPUS:85049323323
SN - 2045-2322
VL - 8
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 2722
ER -