Abstract

The main biochemical changes which occur, when maturation is induced in isolatedX. laevis oocytes by the addition of progesterone to the medium, are discussed. The following points are presented: 1. The peripheric region of the oocyte contains a specific receptor for progesterone; it is a protein with a sedimentation constant of 15–18S. 2. It is doubtful that cAMP plays a direct role in the initiation of maturation. 3. Experiments with inhibitors (KCN, dinitrophenol) show that maturation requires the production of energy. 4. There is no DNA synthesis — except mito-chondrial DNA synthesis — during maturation; the latter is possible in the presence of inhibitors of DNA synthesis (hydroxyurea, 2'-d-adenosine, cytosine arabinoside, bromodeoxyuridine, dimethylbenzyl-rifampicine, ethidium bromide, X-rays). 5. Actinomycin D and, to a lesser extent, α-amanitin speed up maturation. Cordycepin has no effect on this process. 6. Protein synthesis is required for maturation; but experiments with cycloheximide and puromycin have shown that the breakdown of the germinal vesicle (G.V.) is still possible when protein synthesis is inhibited by 50%. Progesterone induces a transient increase in protein synthesis, which is followed by a strong inhibition. 7. Progesterone induces the synthesis or release of 2 antagonistic factors: one of them (MPF) promotes maturation; the other (PIF) produces a special kind of abortive maturation, which has been calledpseudomaturation. PIF becomes detectable several hours before MPF; it produces, after injection into the oocytes, an 80 to 90% inhibition of protein synthesis. Preliminary characterization of PIF indicates that it is neither a protease nor a ribonuclease. It is localized in the outer part of the oocyte and is, in part, attached to membranes. It is thermolabile, non dialyzable.

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