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Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development.

Authors :
Nishikawa M
Matsuki T
Hamada N
Nakayama A
Ito H
Nagata KI
Source :
Medical molecular morphology [Med Mol Morphol] 2023 Dec; Vol. 56 (4), pp. 266-273. Date of Electronic Publication: 2023 Jul 04.
Publication Year :
2023

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.<br /> (© 2023. The Author(s) under exclusive licence to The Japanese Society for Clinical Molecular Morphology.)

Details

Language :
English
ISSN :
1860-1499
Volume :
56
Issue :
4
Database :
MEDLINE
Journal :
Medical molecular morphology
Publication Type :
Academic Journal
Accession number :
37402055
Full Text :
https://doi.org/10.1007/s00795-023-00364-x