Faculty Research 1990 - 1999

Title

Translational regulation of the gradual increase in histone H1 kinase activity in maturing mouse oocytes.

Document Type

Article

Publication Date

1995

Keywords

Cyclins: bi, me, Cycloheximide, Ethers-Cyclic, Female, Gene-Expression-Regulation-Enzymologic: de, In-Vitro, Mice, Mice-Inbred-C57BL, Oocytes: de, en, gd, Oogenesis: de, ge, ph, Protamine-Kinase: ge, Proteins: bi, SUPPORT-NON-U-S-GOVT, SUPPORT-U-S-GOVT-P-H-S, Translation-Genetic: de

JAX Source

Mol Reprod Dev 1995 Jan;40(1):9-15

Grant

HD20575/HD/NICHD

Abstract

In maturing mouse oocytes, p34cdc2-associated histone H1 kinase activity gradually increases until it reaches its maximum at metaphase I (Choi et al., 1991: Development 113:789-795). In this study, treatment of oocytes with cycloheximide resulted in a failure to increase the level of histone H1 activity above that detected at approximately the time of germinal vesicle breakdown (GVB), which is approximately 20-30% of the level normally achieved at metaphase I. Cyclin B was detected in GV-stage oocytes, but there was a 2-2.5-fold increase in the amount of cyclin B in maturing oocytes from GV-stage to metaphase I and a burst of cyclin B synthesis during the first 3 hr of maturation. Okadaic acid-treatment of mouse oocytes did not accelerate activation of histone H1 kinase but rather arrested its activity at the same level observed in cycloheximide-treated oocytes. Thus the components of the p34cdc2 kinase activating system in mouse oocytes are apparently not present in GV-stage oocytes in an amount or configuration that would allow maximum kinase activation when meiosis is reinitiated by okadaic acid. Importantly, okadaic acid-treatment dramatically inhibited protein synthesis. Therefore, the inhibition of protein synthesis by okadaic acid probably abrogates the possibility of de novo synthesis of the regulators of p34cdc2 kinase required to drive its activity to the maximum level normally achieved by metaphase I. It is concluded that there is a critical point in driving the continued activation of histone H1 kinase that occurs at approximately the time of GVB. Progression beyond this point requires de novo protein synthesis.(ABSTRACT TRUNCATED AT 250 WORDS)

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