DC Field | Value | Language |
---|---|---|
dc.contributor.author | H T Kim | - |
dc.contributor.author | J H So | - |
dc.contributor.author | S H Jung | - |
dc.contributor.author | D G Ahn | - |
dc.contributor.author | W Koh | - |
dc.contributor.author | Nam-Soon Kim | - |
dc.contributor.author | S H Kim | - |
dc.contributor.author | S Lee | - |
dc.contributor.author | C H Kim | - |
dc.date.accessioned | 2017-04-19T09:26:20Z | - |
dc.date.available | 2017-04-19T09:26:20Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 1471-213X | - |
dc.identifier.uri | 10.1186/1471-213X-11-49 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/10424 | - |
dc.description.abstract | Background: We recently identified a novel oncogene, Cancer-upregulated gene 2 (CUG2), which is essential for kinetochore formation and promotes tumorigenesis in mammalian cells. However, the in vivo function of CUG2 has not been studied in animal models. Results: To study the function of CUG2 in vivo, we isolated a zebrafish homologue that is expressed specifically in the proliferating cells of the central nervous system (CNS). Morpholino-mediated knockdown of cug2 resulted in apoptosis throughout the CNS and the development of neurodegenerative phenotypes. In addition, cug2-deficient embryos contained mitotically arrested cells displaying abnormal spindle formation and chromosome misalignment in the neural plate. Conclusions: Therefore, our findings suggest that Cug2 is required for normal mitosis during early neurogenesis and has functions in neuronal cell maintenance, thus demonstrating that the cug2 deficient embryos may provide a model system for human neurodegenerative disorders. | - |
dc.publisher | Springer-BMC | - |
dc.title | Cug2 is essential for normal mitotic control and CNS develpment in zebrafish = 제브라피쉬의 중추신경계 발생과 정상적 유사분열 조절에 필수 인자인 Cug2 | - |
dc.title.alternative | Cug2 is essential for normal mitotic control and CNS develpment in zebrafish | - |
dc.type | Article | - |
dc.citation.title | BMC Developmental Biology | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 49 | - |
dc.citation.startPage | 49 | - |
dc.citation.volume | 11 | - |
dc.contributor.affiliatedAuthor | Nam-Soon Kim | - |
dc.contributor.alternativeName | 김현택 | - |
dc.contributor.alternativeName | 소주훈 | - |
dc.contributor.alternativeName | 정승현 | - |
dc.contributor.alternativeName | 안대권 | - |
dc.contributor.alternativeName | 고완수 | - |
dc.contributor.alternativeName | 김남순 | - |
dc.contributor.alternativeName | 김수현 | - |
dc.contributor.alternativeName | 이수진 | - |
dc.contributor.alternativeName | 김철희 | - |
dc.identifier.bibliographicCitation | BMC Developmental Biology, vol. 11, pp. 49-49 | - |
dc.identifier.doi | 10.1186/1471-213X-11-49 | - |
dc.description.journalClass | Y | - |
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