Back to Search
Start Over
NWD1 influences the extension of neuronal axons by regulating microtubule stability.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2024 Nov 19; Vol. 734, pp. 150775. Date of Electronic Publication: 2024 Oct 05. - Publication Year :
- 2024
-
Abstract
- Proteins belonging to the STAND (signal transduction ATPases with numerous domains) family have been implicated in crucial functions across various signal transduction pathways, encompassing both apoptosis and innate immune responses. In this study, we have identified NWD1, a member of the STAND superfamily, as a gene that regulates neurite outgrowth. This was confirmed by siRNA knockdown assay in E18 neurons. A zebrafish model was utilized to create NWD1 knockdown using the NgAgo-gDNA system, revealing the significant role of NWD1 in neurogenesis. We further revealed that NWD1 siRNA reduced the acetylated tubulin protein, and changed the ratio of soluble and polymerized tubulin. Moreover, we investigated the mechanism underlying the regulation of NWD1-mediated microtubule dynamics, and MAP1B may be a target gene. This research unveiled, for the first time, the potential role of NWD1 in regulating axon outgrowth through modulating the ratio of acetylated tubulin.<br />Competing Interests: Declaration of competing interest The authors declared that they have no conflicts of interest with the contents of this article.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Acetylation
Microtubule-Associated Proteins metabolism
Microtubule-Associated Proteins genetics
Neuronal Outgrowth
Neurogenesis
Neurons metabolism
Adenosine Triphosphatases metabolism
Adenosine Triphosphatases genetics
Gene Knockdown Techniques
Cells, Cultured
Humans
Zebrafish Proteins metabolism
Zebrafish Proteins genetics
Microtubules metabolism
Zebrafish metabolism
Zebrafish genetics
Axons metabolism
Tubulin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 734
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 39383832
- Full Text :
- https://doi.org/10.1016/j.bbrc.2024.150775