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Mos positively regulates Xe-Wee1 to lengthen the first mitotic cell cycle of Xenopus

  1. Author:
    Murakami, M. S.
    Copeland, T. D.
    Vande Woude, G. F.
  2. Author Address

    Vande Woude GF NCI, Frederick Canc Res & Dev Ctr, Div Basic Sci Frederick, MD 21702 USA NCI, Frederick Canc Res & Dev Ctr, Div Basic Sci Frederick, MD 21702 USA NCI, Frederick Canc Res & Dev Ctr, ABL, Basic Res Program Frederick, MD 21702 USA
    1. Year: 1999
  1. Journal: Genes & Development
    1. 13
    2. 5
    3. Pages: 620-631
  2. Type of Article: Article
  1. Abstract:

    Several key developmental events occur in the first mitotic cell cycle of Xenopus; consequently this cycle has two gap phases and is similar to 60-75 min in length. In contrast, embryonic cycles 2-12 consist only of S and M phases and are 30 min in length. Xe-Wee1 and Mos are translated and degraded in a developmentally regulated manner. Significantly, both proteins are present in the first cell cycle. We showed previously that the expression of nondegradable Mos, during early interphase, delays the onset of M phase in the early embryonic cell cycles. Here we report that Xe-Wee1 is required for the Mos-mediated NI-phase delay. We find that Xe-Wee1 tyrosine autophosphorylation positively regulates Xe-Wee1 and is only detected in the first 30 min of the first cell cycle. The level and duration of Xe-Wee1 tyrosine phosphorylation is elevated significantly when the first cell cycle is elongated with nondegradable Mos. Importantly, we show that the tyrosine phosphorylation of Xe-Wee1 is required for the Mos-mediated M-phase delay. These findings indicate that Mos positively regulates Xe-Wee1 to generate the G(2) phase in the first cell cycle and establish a direct link between the MAPK signal transduction pathway and Wee1 in vertebrates. [References: 90]

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