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Abstract
The function of cyclin B1 (CB1) and cyclin B2 (CB2) during
porcine oocyte maturation was investigated by injecting
oocytes with their antisense RNAs (asRNAs). At first,
protein levels of both cyclin Bs were examined by
immunoblotting, revealing that immature oocytes had only
CB2, at a level comparable to 1/20 to 1/40 of that
detected in first metaphase oocytes. Both cyclin B
syntheses were started around germinal vesicle breakdown
(GVBD); CB1 and CB2 peaked at the second metaphase and
first metaphase, respectively. We obtained a porcine CB2
cDNA fragment, which was 88% homologous with human CB2, by
RT-PCR using total RNAs of immature porcine oocytes and a
primer set of human CB2. Specific asRNAs of CB1 and CB2
were prepared in vitro. Then one or the other or both was
injected into the cytoplasm of immature oocytes. CB1 asRNA
inhibited CB1 synthesis specifically; the injected oocytes
underwent first meiosis normally but could not arrest at
the second meiotic metaphase. CB2 asRNA inhibited CB2
synthesis specifically, but had almost no effect on the
maturation of injected oocytes. When both CB1 and CB2
asRNAs were injected, synthesis of both cyclin Bs was
inhibited and GVBD was significantly suppressed but
occurred slowly. These results suggest that CB1 is the
principal molecule for regulation in mammalian oocyte
maturation, whereas CB2 has only accessory role. They also
show that, in porcine oocytes, cyclin B synthesis is not
necessary for GVBD induction itself, but synthesis of at
least one cyclin B, CB1 or CB2, is necessary for GVBD
induction in a normal time-course.
Key words:
Gamete Biology
Kinases
Meiosis
Oocyte development
Ovum
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