Prophase I arrest and progression to metaphase I in mouse oocytes are controlled by Emi1-dependent regulation of APC(Cdh1)

dc.contributor.authorMarangos, P.en
dc.contributor.authorVerschuren, E. W.en
dc.contributor.authorChen, R.en
dc.contributor.authorJackson, P. K.en
dc.contributor.authorCarroll, J.en
dc.date.accessioned2015-11-24T16:33:51Z
dc.date.available2015-11-24T16:33:51Z
dc.identifier.issn0021-9525-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/7723
dc.rightsDefault Licence-
dc.subject3T3 Cellsen
dc.subjectAnimalsen
dc.subjectCell Cycle Proteins/*metabolismen
dc.subjectCyclin B/metabolismen
dc.subjectEmbryo, Mammalian/cytology/metabolismen
dc.subjectF-Box Proteins/*metabolismen
dc.subjectFemaleen
dc.subjectGene Expression Regulationen
dc.subjectHumansen
dc.subjectMeiosisen
dc.subject*Meiotic Prophase Ien
dc.subject*Metaphaseen
dc.subjectMiceen
dc.subjectMitotic Spindle Appaen
dc.titleProphase I arrest and progression to metaphase I in mouse oocytes are controlled by Emi1-dependent regulation of APC(Cdh1)en
heal.abstractMammalian oocytes are arrested in prophase of the first meiotic division. Progression into the first meiotic division is driven by an increase in the activity of maturation-promoting factor (MPF). In mouse oocytes, we find that early mitotic inhibitor 1 (Emi1), an inhibitor of the anaphase-promoting complex (APC) that is responsible for cyclin B destruction and inactivation of MPF, is present at prophase I and undergoes Skp1-Cul1-F-box/betaTrCP-mediated destruction immediately after germinal vesicle breakdown (GVBD). Exogenous Emi1 or the inhibition of Emi1 destruction in prophase-arrested oocytes leads to a stabilization of cyclin B1-GFP that is sufficient to trigger GVBD. In contrast, the depletion of Emi1 using morpholino oligonucleotides increases cyclin B1-GFP destruction, resulting in an attenuation of MPF activation and a delay of entry into the first meiotic division. Finally, we show that Emi1-dependent effects on meiosis I require the presence of Cdh1. These observations reveal a novel mechanism for the control of entry into the first meiotic division: an Emi1-dependent inhibition of APC(Cdh1).en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1083/jcb.200607070-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/17190794-
heal.journalNameJ Cell Biolen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2007-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιώνel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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