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JBC, Vol. 252, Issue 5, 1712-1718, Mar, 1977
J. L. Maller and E. G. Krebs
Ripe Xenopus oocytes in first meiotic prophase when incubated with
progesterone in vitro progress synchronously in 3 to 5 h without interphase
to second meiotic metaphase where they remain until fertilization or
activation. Using highly purified preparations of regulatory and catalytic
subunits of adenosine 3':5'-monophosphate-dependent protein kinase from
muscle, this progesterone-stimulated cell division sequence was found to be
inhibited by microinjection of the catalytic subunit and induced directly
in the absence of progesterone after microinjection of regulatory subunit.
Dose-response curves revealed that half-maximal effects of regulatory and
catalytic subunits occurred at an internal concentration of approximately
0.1 muM. These results indicate that the catalytic subunit is necessary and
sufficient to block progesterone-stimulated meiotic cell division. Other
experiments revealed that the catalytic subunit was inhibitory only during
the first hour after progesterone exposure, suggesting that initial steps
in meiotic cell division are affected. Control experiments demonstrate that
the muscle cAMP-dependent protein kinase subunits may interact with the
endogenous oocyte protein kinase. The results support a model in which
meiotic cell division is regulated by a phosphoprotein subject to control
by cAMP-dependent protein kinase.
Progesterone-stimulated meiotic cell division in Xenopus oocytes. Induction by regulatory subunit and inhibition by catalytic subunit of adenosine 3':5'-monophosphate-dependent protein kinase
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