Quantitative analysis of retromer complex-related genes during embryo development in the mouse

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dc.contributor.authorSang Je Park-
dc.contributor.authorJae Won Huh-
dc.contributor.authorYoung-Hyun Kim-
dc.contributor.authorJi Su Kim-
dc.contributor.authorBong Seok Song-
dc.contributor.authorSang Rae Lee-
dc.contributor.authorSun-Uk Kim-
dc.contributor.authorH S Kim-
dc.contributor.authorK Imakawa-
dc.contributor.authorKyu Tae Chang-
dc.date.accessioned2017-04-19T09:23:27Z-
dc.date.available2017-04-19T09:23:27Z-
dc.date.issued2011-
dc.identifier.issn1016-8478-
dc.identifier.uri10.1007/s10059-011-0272-7ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/10140-
dc.description.abstractThe retromer complex is a heteropentameric protein unit associated with retrograde transport of cargo proteins from endosomes to the trans-Golgi network. Functional silencing study of the Vps26a gene indicated the important role of the retromer complex during early developmental stages in the mouse. However, individual expression patterns and quantitative analysis of individual members of the retromer complex during the early developmental stages has not been investigated. In this study, we conducted quantitative expression analysis of six retromer complex genes (Vps26a, Vps26b, Vps29, Vps35, Snx1, and Snx2) and one related receptor gene (Ci-mpr) during the eleven embryonic stages with normal MEF (mouse embryonic fibroblast) and Vps26a-/- MEF cells. Remarkably, except for Vps26a (maternal expression pattern), all tested genes showed maternal-zygotic expression patterns. And five genes (Vps26b, Vps29, Vps35, Snx2, and Ci-mpr) showed a pattern of decreased expression in Vps26a-/- MEF cells by comparative analysis between normal MEF and Vps26a-/- MEF cells. However, the Snx1 gene showed a pattern of increased expression in Vps26a-/- MEF cells. From our results, we could assume that retromer complexrelated genes have important roles during oocyte development. However, in the preimplantation stage, they did not have significant roles.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleQuantitative analysis of retromer complex-related genes during embryo development in the mouse-
dc.title.alternativeQuantitative analysis of retromer complex-related genes during embryo development in the mouse-
dc.typeArticle-
dc.citation.titleMolecules and Cells-
dc.citation.number5-
dc.citation.endPage436-
dc.citation.startPage431-
dc.citation.volume31-
dc.contributor.affiliatedAuthorSang Je Park-
dc.contributor.affiliatedAuthorJae Won Huh-
dc.contributor.affiliatedAuthorYoung-Hyun Kim-
dc.contributor.affiliatedAuthorJi Su Kim-
dc.contributor.affiliatedAuthorBong Seok Song-
dc.contributor.affiliatedAuthorSang Rae Lee-
dc.contributor.affiliatedAuthorSun-Uk Kim-
dc.contributor.affiliatedAuthorKyu Tae Chang-
dc.contributor.alternativeName박상제-
dc.contributor.alternativeName허재원-
dc.contributor.alternativeName김영현-
dc.contributor.alternativeName김지수-
dc.contributor.alternativeName송봉석-
dc.contributor.alternativeName이상래-
dc.contributor.alternativeName김선욱-
dc.contributor.alternativeName김희수-
dc.contributor.alternativeNameImakawa-
dc.contributor.alternativeName장규태-
dc.identifier.bibliographicCitationMolecules and Cells, vol. 31, no. 5, pp. 431-436-
dc.identifier.doi10.1007/s10059-011-0272-7-
dc.subject.keywordmouse embryo-
dc.subject.keywordmouse embryonic fibroblast-
dc.subject.keywordreal-time RT-PCR-
dc.subject.keywordretromer complex-
dc.subject.localmouse embryo-
dc.subject.localMouse embryo-
dc.subject.localMouse embryos-
dc.subject.localmouse embryonic fibroblast-
dc.subject.localMouse embryonic fibroblast (MEF)-
dc.subject.localMouse embryonic fibroblasts (MEF)-
dc.subject.localmouse embryonic fibroblasts-
dc.subject.localMouse embryonic fibroblasts-
dc.subject.localReal-time RT-PCR-
dc.subject.localreal-time RT-PCR-
dc.subject.localRetromer complex-
dc.subject.localretromer complex-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > National Primate Research Center > 1. Journal Articles
Jeonbuk Branch Institute > Primate Resources Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > Futuristic Animal Resource & Research Center > 1. Journal Articles
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