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dc.contributor.authorIshikawa, Tokiroen
dc.contributor.authorToyama, Takuyaen
dc.contributor.authorNakamura, Yukien
dc.contributor.authorTamada, Kentaroen
dc.contributor.authorShimizu, Hitomien
dc.contributor.authorNinagawa, Satoshien
dc.contributor.authorOkada, Tetsuyaen
dc.contributor.authorKamei, Yasuhiroen
dc.contributor.authorIshikawa-Fujiwara, Tomokoen
dc.contributor.authorTodo, Takeshien
dc.contributor.authorAoyama, Erikoen
dc.contributor.authorTakigawa, Masaharuen
dc.contributor.authorHarada, Akihiroen
dc.contributor.authorMori, Kazutoshien
dc.contributor.alternative石川, 時郎ja
dc.contributor.alternative遠山, 拓也ja
dc.contributor.alternative中村, 有貴ja
dc.contributor.alternative玉田, 健太郎ja
dc.contributor.alternative清水, 瞳ja
dc.contributor.alternative蜷川, 暁ja
dc.contributor.alternative岡田, 徹也ja
dc.contributor.alternative森, 和俊ja
dc.date.accessioned2017-09-06T05:38:54Z-
dc.date.available2017-09-06T05:38:54Z-
dc.date.issued2017-06-05-
dc.identifier.issn0021-9525-
dc.identifier.urihttp://hdl.handle.net/2433/227005-
dc.description.abstractThe unfolded protein response (UPR) handles unfolded/misfolded proteins accumulated in the endoplasmic reticulum (ER). However, it is unclear how vertebrates correctly use the total of ten UPR transducers. We have found that ER stress occurs physiologically during early embryonic development in medaka fish and that the smooth alignment of notochord cells requires ATF6 as a UPR transducer, which induces ER chaperones for folding of type VIII (short-chain) collagen. After secretion of hedgehog for tissue patterning, notochord cells differentiate into sheath cells, which synthesize type II collagen. In this study, we show that this vacuolization step requires both ATF6 and BBF2H7 as UPR transducers and that BBF2H7 regulates a complete set of genes (Sec23/24/13/31, Tango1, Sedlin, and KLHL12) essential for the enlargement of COPII vesicles to accommodate long-chain collagen for export, leading to the formation of the perinotochordal basement membrane. Thus, the most appropriate UPR transducer is activated to cope with the differing physiological ER stresses of different content types depending on developmental stage.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherRockefeller University Pressen
dc.rights© 2017 Ishikawa et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).en
dc.subjectDevelopmenten
dc.subjectProtein Homeostasisen
dc.titleUPR transducer BBF2H7 allows export of type II collagen in a cargo- and developmental stage–specific manneren
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleThe Journal of Cell Biologyen
dc.identifier.volume216-
dc.identifier.issue6-
dc.identifier.spage1761-
dc.identifier.epage1774-
dc.relation.doi10.1083/jcb.201609100-
dc.textversionpublisher-
dc.identifier.pmid28500182-
dcterms.accessRightsopen access-
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