Protective Role of Cell Division Cycle 48 (CDC48) Protein against Neurodegeneration via Ubiquitin-Proteasome System Dysfunction during Zebrafish Development
- Authors
- Imamura, S., Yabu, T., and Yamashita, M.
- ID
- ZDB-PUB-120503-23
- Date
- 2012
- Source
- The Journal of biological chemistry 287(27): 23047-23056 (Journal)
- Registered Authors
- Yamashita, Michiaki
- Keywords
- autophagy, development, molecular chaperone, neurodegeneration, proteasome, ubiquitination, zebrafish, CDC48, VCP, p97
- MeSH Terms
-
- Adenosine Triphosphatases/chemistry
- Adenosine Triphosphatases/genetics
- Adenosine Triphosphatases/metabolism*
- Animals
- Cell Cycle Proteins/chemistry
- Cell Cycle Proteins/genetics
- Cell Cycle Proteins/metabolism*
- Cell Division/physiology
- Diencephalon/abnormalities
- Diencephalon/metabolism
- Gene Expression Regulation, Developmental/physiology
- Gene Expression Regulation, Enzymologic/physiology
- Mesencephalon/abnormalities
- Mesencephalon/metabolism
- Motor Neurons/cytology
- Motor Neurons/metabolism
- Nerve Degeneration/metabolism*
- Nerve Degeneration/physiopathology
- Phenotype
- Proteasome Endopeptidase Complex/metabolism*
- Protein Structure, Tertiary
- Retinal Ganglion Cells/cytology
- Retinal Ganglion Cells/enzymology
- Spinal Cord/abnormalities
- Spinal Cord/metabolism
- Ubiquitin/metabolism*
- Zebrafish/embryology*
- Zebrafish/genetics
- Zebrafish/metabolism*
- PubMed
- 22549779 Full text @ J. Biol. Chem.
Cell division cycle 48 (CDC48), a ubiquitin-dependent molecular chaperone, is thought to mediate a variety of degradative and regulatory processes and maintain cellular homoeostasis. To investigate the protective function of CDC48 against accumulated ubiquitinated proteins during neurodevelopment, we developed an in vivo bioassay technique that detects expression and accumulation of fluorescent proteins with a poly-ubiquitination signal at the N-terminus. When we introduced CDC48 antisense morpholino oligonucleotides into zebrafish embryos, the morphant embryos were lethal and showed defects in neuronal outgrowth and neurodegeneration, and poly-ubiquitinated fluorescent proteins accumulated in the inner plexiform and ganglion cell layers, as well as the diencephalon and mesencephalon, indicating that the degradation of poly-ubiquitinated proteins by the ubiquitin-proteasome system (UPS) was blocked. These abnormal phenotypes in the morphant were rescued by CDC48 or human VCP overexpression. Therefore, the protective function of CDC48 is essential for neurodevelopment.