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Cited 3 time in webofscience Cited 3 time in scopus
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Cell cycle arrest mediated by WEE1 is involved in the unfolded protein response in plants

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dc.contributor.authorKo, Ki Seong-
dc.contributor.authorYoo, Jae Yong-
dc.contributor.authorRamasamy, Nirmal Kumar-
dc.contributor.authorHarmoko, Rikno-
dc.contributor.authorVu, Bich Ngoc Thi-
dc.contributor.authorPark, Ji Ye-
dc.contributor.authorLee, Kyun Oh-
dc.date.accessioned2022-12-26T16:33:58Z-
dc.date.available2022-12-26T16:33:58Z-
dc.date.issued2018-10-
dc.identifier.issn1863-5466-
dc.identifier.issn1863-5474-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/11198-
dc.description.abstractActivation of the unfolded protein response (UPR) in mammalian cells leads to cell cycle arrest at the G1 phase (Thomas et al., J Biol Chem 288:7606-7617, 2013). However, how UPR signaling affects cell cycle arrest remains largely unknown in plants. Here, we examined UPR and endoreduplication in Col-0, wee1, and ER stress sensing-deficient ire1a&b plants during DNA replication and ER stress conditions. We found that WEE1, an essential negative regulator of the cell cycle, is involved in the maintenance of ER homeostasis during genotoxic stress and the ER stress hypersensitivity of ire1a&b is alleviated by loss-of-function mutation in WEE1. WEE1-mediated cell cycle arrest was required for IRE1-bZIP60 pathway activation during ER stress. In contrast, loss-of-function mutation in WEE1 caused increased expression of UPR-related genes during DNA replication stress. WEE1 and IRE1 were required for endoreduplication during DNA replication stress and ER stress, respectively. Taken together, these findings suggest that cell cycle regulation is associated with UPR activation in different manners during ER stress and DNA replication stress in Arabidopsis.-
dc.format.extent14-
dc.language영어-
dc.language.isoENG-
dc.publisherSPRINGER-
dc.titleCell cycle arrest mediated by WEE1 is involved in the unfolded protein response in plants-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1007/s11816-018-0496-5-
dc.identifier.scopusid2-s2.0-85053063169-
dc.identifier.wosid000450181000003-
dc.identifier.bibliographicCitationPLANT BIOTECHNOLOGY REPORTS, v.12, no.5, pp 315 - 328-
dc.citation.titlePLANT BIOTECHNOLOGY REPORTS-
dc.citation.volume12-
dc.citation.number5-
dc.citation.startPage315-
dc.citation.endPage328-
dc.type.docTypeArticle-
dc.identifier.kciidART002403533-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaPlant Sciences-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryPlant Sciences-
dc.subject.keywordPlusENDOPLASMIC-RETICULUM STRESS-
dc.subject.keywordPlusDNA-DAMAGE-
dc.subject.keywordPlusTRANSCRIPTION FACTOR-
dc.subject.keywordPlusDEPENDENT-KINASE-
dc.subject.keywordPlusROOT-GROWTH-
dc.subject.keywordPlusARABIDOPSIS-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusCHECKPOINT-
dc.subject.keywordPlusDIVISION-
dc.subject.keywordPlusGENE-
dc.subject.keywordAuthorGenotoxic stress-
dc.subject.keywordAuthorER stress-
dc.subject.keywordAuthorUPR-
dc.subject.keywordAuthorER homeostasis-
dc.subject.keywordAuthorCell cycle arrest-
dc.subject.keywordAuthorEndoreduplication-
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