THE SIGNAL CASCADE FOR THE ACTIVATION OF PROTEIN-SYNTHESIS DURING THEMATURATION OF STARFISH OOCYTES - A ROLE FOR PROTEIN-KINASE-C AND HOMOLOGIES WITH MATURATION IN XENOPUS AND MAMMALIAN OOCYTES
Mb. Hille et al., THE SIGNAL CASCADE FOR THE ACTIVATION OF PROTEIN-SYNTHESIS DURING THEMATURATION OF STARFISH OOCYTES - A ROLE FOR PROTEIN-KINASE-C AND HOMOLOGIES WITH MATURATION IN XENOPUS AND MAMMALIAN OOCYTES, INVERTEBRATE REPRODUCTION & DEVELOPMENT, 30(1-3), 1996, pp. 81-97
The goal of a growing oocyte is to prepare the female gamete for the r
apid cleavages that follow fertilization. The oocyte stores proteins a
nd mRNAs required for meiosis and mitosis, since little or no transcri
ption of new mRNAs occurs during the early cleavage stages of most ani
mal embryos. Immature oocytes of mammals, amphibians, and starfish are
arrested in the prophase of meiosis I. Meiotic maturation of these oo
cytes is induced by a maturation hormone that reinitiates meiosis, com
pletes the nuclear reduction of meiosis I and meiosis II, prepares the
oocytes for activation by the male gametes, and activates stores of p
roteins and mRNAs needed for the early cleavage stages. Maturation hor
mones induce at least three distinct and parallel molecular pathways i
n animal oocytes: the activation of the maturation promotion factor (M
PF); the activation and polyadenylation of mRNAs stored during oogenes
is; the activation of the protein synthesis machinery of the oocyte, w
hich is required to translate the newly activated mRNAs. We review her
e (1) biological changes that occur during oocyte maturation, (2) sign
al pathways that stimulate and coordinate maturation in starfish, Xeno
pus, and mammalian oocytes, (3) components of the protein synthesis ma
chinery that are activated during oocyte maturation, including (4) the
phosphorylation of mRNA cap binding protein, eukaryotic initiation fa
ctor 4 (eIF-4E), and (5) a potential role for protein kinase C in phos
phorylating eIF-4E and activating MPF in starfish oocytes. Finally, we
propose that the modulation of a trimeric G-protein leads to the obse
rved decrease in cyclic adenosine monophosphate (cAMP) levels and the
subsequent activation of a pivotal serine/threonine kinase that activa
tes MPF, stored mRNAs, and the protein synthesis machinery.