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Miyazaki, Haruko Department of Molecular Biology and Biochemistry, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
Nishioka, Saki Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University
Yamanaka, Tomoyuki Laboratory of Structural Neuropathology, Graduate School of Brain Science, Doshisha University
Abe, Manabu Department of Animal Model Development, Brain Research Institute, Niigata University
Imamura, Yukio Laboratory of Structural Neuropathology, Graduate School of Brain Science, Doshisha University
Miyasaka, Tomohiro Faculty of Life and Medical Sciences, Doshisha University
Kakuda, Nobuto Faculty of Life and Medical Sciences, Doshisha University
Oohashi, Toshitaka Department of Molecular Biology and Biochemistry, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine ORCID Kaken ID publons researchmap
Shimogori, Tomomi Laboratory for Molecular Mechanisms of Brain Development, RIKEN Center for Brain Science
Yamakawa, Kazuhiro Laboratory for Neurogenetics, RIKEN Center for Brain Science
Ikawa, Masahito Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University
Nukina, Nobuyuki Laboratory of Structural Neuropathology, Graduate School of Brain Science, Doshisha University
Abstract
Golli–myelin basic proteins, encoded by the myelin basic protein gene, are widely expressed in neurons and oligodendrocytes in the central nervous system. Further, prior research has shown that Golli–myelin basic protein is necessary for myelination and neuronal maturation during central nervous system development. In this study, we established Golli–myelin basic protein-floxed mice to elucidate the cell-type-specific effects of Golli–myelin basic protein knockout through the generation of conditional knockout mice (Golli–myelin basic proteinsfl/fl; E3CreN), in which Golli–myelin basic proteins were specifically deleted in cerebellar granule neurons, where Golli–myelin basic proteins are expressed abundantly in wild-type mice. To investigate the role of Golli–myelin basic proteins in cerebellar granule neurons, we further performed histopathological analyses of these mice, with results indicating no morphological changes or degeneration of the major cellular components of the cerebellum. Furthermore, behavioral analysis showed that Golli–myelin basic proteinsfl/fl; E3CreN mice were healthy and did not display any abnormal behavior. These results suggest that the loss of Golli–myelin basic proteins in cerebellar granule neurons does not lead to cerebellar perturbations or behavioral abnormalities. This mouse model could therefore be employed to analyze the effect of Golli–myelin basic protein deletion in specific cell types of the central nervous system, such as other neuronal cells and oligodendrocytes, or in lymphocytes of the immune system.
Keywords
Golli-MBP
Cerebellar granule neuron
CRISPR/Cas9
Conditional knockout
Note
The version of record of this article, first published in Transgenic Research, is available online at Publisher’s website: http://dx.doi.org/10.1007/s11248-024-00382-0
Published Date
2024-04-29
Publication Title
Transgenic Research
Volume
volume33
Issue
issue3
Publisher
Springer Science and Business Media LLC
Start Page
99
End Page
117
ISSN
0962-8819
NCID
AA10873487
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Author(s) 2024
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isVersionOf https://doi.org/10.1007/s11248-024-00382-0
License
http://creativecommons.org/licenses/by/4.0/
Citation
Miyazaki, H., Nishioka, S., Yamanaka, T. et al. Generation and characterization of cerebellar granule neurons specific knockout mice of Golli-MBP. Transgenic Res 33, 99–117 (2024). https://doi.org/10.1007/s11248-024-00382-0
助成情報
( Okayama University )