Neuron-Specific Expression of atp6v0c2 in Zebrafish CNS
- Authors
- Chung, Ah-Young; Kim, Myoung-Jin; Kim, Dohyun; Bang, Sangsu; Hwang, Sun Wook; Lim, Chae Seung; Lee, Sanggyu; Park, Hae-Chul; Huh, Tae-Lin
- Issue Date
- Sep-2010
- Publisher
- WILEY
- Keywords
- V-ATPase; neuron; Notch signaling; zebrafish
- Citation
- DEVELOPMENTAL DYNAMICS, v.239, no.9, pp.2501 - 2508
- Indexed
- SCIE
SCOPUS
- Journal Title
- DEVELOPMENTAL DYNAMICS
- Volume
- 239
- Number
- 9
- Start Page
- 2501
- End Page
- 2508
- URI
- https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/14582
- DOI
- 10.1002/dvdy.22383
- ISSN
- 1058-8388
- Abstract
- Vacuolar ATPase (V-ATPase) is a multi-subunit enzyme that plays an important role in the acidification of a variety of intracellular compartments. ATP6V0C is subunit c of the V-o domain that forms the proteolipid pore of the enzyme. In the present study, we investigated the neuron-specific expression of atp6v0c2, a novel isoform of the V-ATPase c-subunit, during the development of the zebrafish CNS. Zebrafish atp6v0c2 was isolaled from a genome-wide analysis of the zebrafish mib(ta52b) mutant designed to identify genes differentially regulated by Notch signaling. Whole-mount in situ hybridization revealed that atp6v0c2 is expressed in a subset of CNS neurons beginning several hours after the emergence of post-mitotic neurons. The ATP6V0C2 protein is co-localized with the presynaptic vesicle marker, SV2, suggesting that it is involved in neurotransmitter storage and/or secretion in neurons. In addition, the loss-of-function experiment suggests that ATP6VOC2 is involved in the control of neuronal excitability. Developmental Dynamics 239:2501-2508, 2010. (C) 2010 Wiley-Liss, Inc.
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- Appears in
Collections - 2. Clinical Science > Department of Laboratory Medicine > 1. Journal Articles
- 3. Graduate School > Biomedical Research Center > 1. Journal Articles

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