REQUIREMENT FOR PROTEIN-SYNTHESIS DURING THE ONSET OF MEIOSIS IN BOVINE OOCYTES AND ITS INVOLVEMENT IN THE AUTOCATALYTIC AMPLIFICATION OF MATURATION-PROMOTING FACTOR

被引:32
作者
TATEMOTO, H
HORIUCHI, T
机构
[1] Laboratory of Reproductive Biology, Department of Bioresources, Hiroshima Prefectural University, Hiroshima, Shobara
关键词
CYCLOHEXIMIDE; OKADAIC ACID; ELECTROFUSION; GVBD;
D O I
10.1002/mrd.1080410108
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The present study was carried out using the method of electrofusion, or treatment with okadaic acid (OA), to determine whether protein synthesis at the onset of culture was required for the meiotic resumption of bovine follicular oocytes. Germinal vesicle breakdown (GVBD) occurred in bovine oocytes at 6 hr after separation from their follicles in vitro. Following this, immature germinal vesicle (GV) oocytes, preincubated for 0, 2, 4, and 6 hr, were fused to mature oocytes. When immature oocytes, preincubated for 0 hr, were fused to mature oocytes and then cultured for 3 hr in basic medium, GVBD was observed in all fused cells, whereas in the case of cultivation in medium supplemented with the protein synthesis inhibitor (25 mu g/ml cycloheximide; CX), 39% of the fused cells possessed an intact GV within their cytoplasm. In immature oocytes preincubated for 4 or 6 hr, however, this proportion was significantly reduced to 7% and 4%, respectively, without protein synthesis after fusion. In addition, the CX-dependent block of GVBD could be overcome in only 13% of bovine follicular oocytes by the addition of 2 mu M OA, although 51% of oocytes which synthesized the protein during the first 6 hr of culture induced GVBD in subsequent culture with CX plus OA. Thus, we conclude that the initiation of GVBD in bovine oocytes requires protein synthesized at the onset of meiosis, which is related to the autocatalytic amplification of the maturation-promoting factor. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:47 / 53
页数:7
相关论文
共 33 条
[1]  
BALAKIER H, 1978, EXP CELL RES, V112, P137, DOI 10.1016/0014-4827(78)90534-7
[2]  
CHOI T, 1991, DEVELOPMENT, V113, P789
[3]   MATURATION IN VITRO OF MOUSE SHEEP COW PIG RHESUS MONKEY AND HUMAN OVARIAN OOCYTES [J].
EDWARDS, RG .
NATURE, 1965, 208 (5008) :349-&
[4]  
FULKA J, 1986, J REPROD FERTIL, V77, P281, DOI 10.1530/jrf.0.0770281
[5]   DOES AUTOCATALYTIC AMPLIFICATION OF MATURATION-PROMOTING FACTOR (MPF) EXIST IN MAMMALIAN OOCYTES [J].
FULKA, J ;
FLECHON, JE ;
MOTLIK, J ;
FULKA, J .
GAMETE RESEARCH, 1988, 21 (02) :185-192
[6]   CYCLIN IS A COMPONENT OF MATURATION-PROMOTING FACTOR FROM XENOPUS [J].
GAUTIER, J ;
MINSHULL, J ;
LOHKA, M ;
GLOTZER, M ;
HUNT, T ;
MALLER, JL .
CELL, 1990, 60 (03) :487-494
[7]   CELL-CYCLE DYNAMICS OF AN M-PHASE-SPECIFIC CYTOPLASMIC FACTOR IN XENOPUS-LAEVIS OOCYTES AND EGGS [J].
GERHART, J ;
WU, M ;
KIRSCHNER, M .
JOURNAL OF CELL BIOLOGY, 1984, 98 (04) :1247-1255
[8]   OKADAIC ACID, A SPECIFIC PROTEIN PHOSPHATASE INHIBITOR, INDUCES MATURATION AND MPF FORMATION IN XENOPUS-LAEVIS OOCYTES [J].
GORIS, J ;
HERMANN, J ;
HENDRIX, P ;
OZON, R ;
MERLEVEDE, W .
FEBS LETTERS, 1989, 245 (1-2) :91-94
[9]   REGULATION OF MEIOTIC METAPHASE BY A CYTOPLASMIC MATURATION-PROMOTING FACTOR DURING MOUSE OOCYTE MATURATION [J].
HASHIMOTO, N ;
KISHIMOTO, T .
DEVELOPMENTAL BIOLOGY, 1988, 126 (02) :242-252
[10]   PHOSPHORYLATION AND ACTIVATION OF HUMAN CDC25-C BY CDC2 CYCLIN-B AND ITS INVOLVEMENT IN THE SELF-AMPLIFICATION OF MPF AT MITOSIS [J].
HOFFMANN, I ;
CLARKE, PR ;
MARCOTE, MJ ;
KARSENTI, E ;
DRAETTA, G .
EMBO JOURNAL, 1993, 12 (01) :53-63