Phosphorylation of mitogen-activated protein kinase cascade during early embryo development in the mouse

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dc.contributor Tojo, Hideaki
dc.contributor Yamanouchi, Keitaro
dc.contributor Goto, Seitaro
dc.contributor Ohashi, Satoshi
dc.contributor Yamashita, Masakane
dc.contributor Kagii, Hideyuki
dc.contributor Sugiura, Koji
dc.contributor Naito, Kunihiko
dc.contributor Iwamori, Naoki
dc.date.accessioned 2012-01-30T12:03:22Z
dc.date.available 2012-01-30T12:03:22Z
dc.date.issued 2000
dc.identifier.citation Rep. Fert. Dev. (2000) 12(4): 209-214
dc.identifier.issn 1031-3613
dc.identifier.uri http://livestocklibrary.com.au/handle/1234/16414
dc.description.abstract The mitogen-activated protein kinase (MAPK) cascade is one of the mostimportant signal transduction pathways that regulate the cell cycle in somaticcells. The present study examined the phosphorylation states of components inthe MAPK cascade, Raf-1, MEK-1, and extracellular signal regulated kinases(ERKs), which are activated by mitogens, throughout early mouse embryodevelopment and in cultured somatic cells generally. In somatic cells, Raf-1and MEK-1 were phosphorylated at M-phase and dephosphorylated duringinterphase. ERKs were not phosphorylated at any stage during the cell cycle.These results were similar to previous findings for the first and second cellcycles of early mouse embryos. In contrast, after the four-cell stage, notonly ERKs, but also Raf-1 and MEK-1, were not phosphorylated at any stageduring the cell cycle in mouse early embryos. These results suggest that theMAPK cascade in mouse embryos is regulated by the same mechanism as in somaticcells before the two-cell stage, and that regulation is changed to anembryo-specific mechanism after the four-cell stage.
dc.publisher CSIRO Publishing
dc.source.uri http://www.publish.csiro.au/?act=view_file&file_id=RD00064.pdf
dc.subject cdc2
dc.subject MPF
dc.subject zygotic gene activation
dc.title Phosphorylation of mitogen-activated protein kinase cascade during early embryo development in the mouse
dc.type Research
dc.description.version Journal article
dc.identifier.volume 12
dc.identifier.page 209-214
dc.identifier.issue 4


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