Abstract
WAC is an adaptor protein involved in gene transcription, protein ubiquitination, and autophagy. Accumulating evidence indicates that WAC gene abnormalities are responsible for neurodevelopmental disorders. In this study, we prepared anti-WAC antibody, and performed biochemical and morphological characterization focusing on mouse brain development. Western blotting analyses revealed that WAC is expressed in a developmental stage-dependent manner. In immunohistochemical analyses, while WAC was visualized mainly in the perinuclear region of cortical neurons at embryonic day 14, nuclear expression was detected in some cells. WAC then came to be enriched in the nucleus of cortical neurons after birth. When hippocampal sections were stained, nuclear localization of WAC was observed in Cornu ammonis 1 – 3 and dentate gyrus. In cerebellum, WAC was detected in the nucleus of Purkinje cells and granule cells, and possibly interneurons in the molecular layer. In primary cultured hippocampal neurons, WAC was distributed mainly in the nucleus throughout the developing process while it was also localized at perinuclear region at 3 and 7 days in vitro. Notably, WAC was visualized in Tau-1-positive axons and MAP2-positive dendrites in a time-dependent manner. Taken together, results obtained here suggest that WAC plays a crucial role during brain development.
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Acknowledgements
We thank Mses. Noriko Kawamura and Nobuko Hane for technical assistance. This work was supported in part by Japan Society for the Promotion of Science (JSPS) KAKENHI Grant-in-Aid for Scientific Research (B) (Grant Number JP22H03049), Grant-in-Aid for Challenging Exploratory Research (JP22K19498), Grant-in-Aid for Scientific Research (C) (JP19K07059), Grant-in-Aid for Research Activity Start-up (JP20K22888), and Grant-in-Aid for Early-Career Scientists (JP21K15895).
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Nishikawa, M., Matsuki, T., Hamada, N. et al. Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development. Med Mol Morphol 56, 266–273 (2023). https://doi.org/10.1007/s00795-023-00364-x
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DOI: https://doi.org/10.1007/s00795-023-00364-x