Cug2 is essential for normal mitotic control and CNS develpment in zebrafish = 제브라피쉬의 중추신경계 발생과 정상적 유사분열 조절에 필수 인자인 Cug2

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dc.contributor.authorH T Kim-
dc.contributor.authorJ H So-
dc.contributor.authorS H Jung-
dc.contributor.authorD G Ahn-
dc.contributor.authorW Koh-
dc.contributor.authorNam-Soon Kim-
dc.contributor.authorS H Kim-
dc.contributor.authorS Lee-
dc.contributor.authorC H Kim-
dc.date.accessioned2017-04-19T09:26:20Z-
dc.date.available2017-04-19T09:26:20Z-
dc.date.issued2011-
dc.identifier.issn1471-213X-
dc.identifier.uri10.1186/1471-213X-11-49ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10424-
dc.description.abstractBackground: 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.publisherSpringer-BMC-
dc.titleCug2 is essential for normal mitotic control and CNS develpment in zebrafish = 제브라피쉬의 중추신경계 발생과 정상적 유사분열 조절에 필수 인자인 Cug2-
dc.title.alternativeCug2 is essential for normal mitotic control and CNS develpment in zebrafish-
dc.typeArticle-
dc.citation.titleBMC Developmental Biology-
dc.citation.number0-
dc.citation.endPage49-
dc.citation.startPage49-
dc.citation.volume11-
dc.contributor.affiliatedAuthorNam-Soon Kim-
dc.contributor.alternativeName김현택-
dc.contributor.alternativeName소주훈-
dc.contributor.alternativeName정승현-
dc.contributor.alternativeName안대권-
dc.contributor.alternativeName고완수-
dc.contributor.alternativeName김남순-
dc.contributor.alternativeName김수현-
dc.contributor.alternativeName이수진-
dc.contributor.alternativeName김철희-
dc.identifier.bibliographicCitationBMC Developmental Biology, vol. 11, pp. 49-49-
dc.identifier.doi10.1186/1471-213X-11-49-
dc.description.journalClassY-
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Division of A.I. & Biomedical Research > Orphan Disease Therapeutic Target Research Center > 1. Journal Articles
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