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PLK1 regulates spindle formation kinetics and APC/C activation in mouse zygote

  1. 1.
    SYSNO ASEP0460308
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitlePLK1 regulates spindle formation kinetics and APC/C activation in mouse zygote
    Author(s) Baran, V. (SK)
    Brzáková, Adéla (UZFG-Y)
    Rehák, P. (SK)
    Kovaříková, V. (CZ)
    Šolc, Petr (UZFG-Y) RID, ORCID
    Source TitleZygote. - : Cambridge University Press - ISSN 0967-1994
    Roč. 24, č. 3 (2016), s. 338-345
    Number of pages8 s.
    Publication formPrint - P
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsAPC/C ; BI2536 ; live cell imaging ; mouse zygote ; PLK1 ; securin ; spindle assembly
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsED2.1.00/03.0124 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LH12057 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportUZFG-Y - RVO:67985904
    UT WOS000376277900003
    EID SCOPUS84968813929
    DOI10.1017/S0967199415000246
    AnnotationPolo-like kinase 1 (PLK1) is involved in essential events of cell cycle including mitosis in which it participates in centrosomal microtubule nucleation, spindle bipolarity establishment and cytokinesis. Although PLK1 function has been studied in cycling cancer cells, only limited data are known about its role in the first mitosis of mammalian zygotes. During the 1-cell stage of mouse embryo development, the acentriolar spindle is formed and the shift from acentriolar to centrosomal spindle formation progresses gradually throughout the preimplantation stage, thus providing a unique possibility to study acentriolar spindle formation. We have shown previously that PLK1 activity is not essential for entry into first mitosis, but is required for correct spindle formation and anaphase onset in 1-cell mouse embryos. In the present study, we extend this knowledge by employing quantitative confocal live cell imaging to determine spindle formation kinetics in the absence of PLK1 activity and answer the question whether metaphase arrest at PLK1-inhibited embryos is associated with low anaphase-promoting complex/cyclosome (APC/C) activity and consequently high securin level. We have shown that inhibition of PLK1 activity induces a delay in onset of acentriolar spindle formation during first mitosis. Although these PLK1-inhibited 1-cell embryos were finally able to form a bipolar spindle, not all chromosomes were aligned at the metaphase equator. PLK1-inhibited embryos were arrested in metaphase without any sign of APC/C activation with high securin levels. Our results document that PLK1 controls the onset of spindle assembly and spindle formation, and is essential for APC/C activation before anaphase onset in mouse zygotes.
    WorkplaceInstitute of Animal Physiology and Genetics
    ContactJana Zásmětová, knihovna@iapg.cas.cz, Tel.: 315 639 554
    Year of Publishing2017
Number of the records: 1  

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