MOLECULAR-CLONING AND IMMUNOLOGICAL ANALYSIS OF GOLDFISH CYCLIN-A DURING OOCYTE MATURATION

Citation
Y. Katsu et al., MOLECULAR-CLONING AND IMMUNOLOGICAL ANALYSIS OF GOLDFISH CYCLIN-A DURING OOCYTE MATURATION, Developmental biology, 170(2), 1995, pp. 616-625
Citations number
57
Categorie Soggetti
Developmental Biology",Biology
Journal title
ISSN journal
00121606
Volume
170
Issue
2
Year of publication
1995
Pages
616 - 625
Database
ISI
SICI code
0012-1606(1995)170:2<616:MAIAOG>2.0.ZU;2-T
Abstract
Cyclin A belongs to a family of proteins involved in the regulation of the eukaryotic cell cycle. Although cyclin A is thought to be involve d in the regulation of both S and M phase, its exact role in the cell cycle, especially in the meiotic cycle (oocyte maturation), is uncerta in. We isolated cyclin A cDNA clones from a goldfish oocyte cDNA libra ry. Monoclonal antibody raised against bacterially produced goldfish c yclin A recognized a 47-kDa protein that disappeared after egg activat ion. Unlike goldfish cyclin B, which is absent in immature oocytes, cy clin A was already present in immature oocytes and its protein level d id not change remarkably during oocyte maturation. These results diffe r from the finding in Xenopus, in which cyclin A is absent, but cyclin B is present, in immature oocytes. Goldfish cyclin A was associated w ith cdc2 kinase in mature oocytes, but not with cdk2. Recombinant cycl in A bound to and activated cdc2 in a cell-free system, but cyclin A a nd cdk2 binding was not observed. The kinase activity of cyclin A-cdc2 was undetectable in immature oocytes and first appeared at about the time of germinal vesicle breakdown (GVBD). In contrast to the cyclin B -cdc2 activity that corresponded to the occurrence of GVBD, cyclin A-c dc2 activity increased only slightly until GVBD was completed and incr eased drastically after the completion of the first meiotic division. Furthermore, microinjection of cyclin A mRNA into immature oocytes did not cause GVBD; however, microinjection of cyclin B mRNA did. These r esults suggest that cyclin A-cdc2 kinase and cyclin B-cdc2 kinase play different roles in controlling oocyte maturation. The roles of cyclin A in the rapid activation of cyclin B-cdc2 kinase at meiosis I and II transition and in the maintenance of high maturation-promoting factor activity in mature unfertilized eggs are discussed. (C) 1995 Academic Press, Inc.