MOUSE OOCYTE MATURATION - MEIOTIC CHECKPOINTS

被引:27
作者
FULKA, J [1 ]
MOOR, RM [1 ]
FULKA, J [1 ]
机构
[1] INST ANIM PROD,CR-10400 PRAGUE 10,CZECH REPUBLIC
关键词
D O I
10.1006/excr.1995.1247
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mouse oocytes at different stages of maturation were fused together and the ensuing cell cycle events were analyzed with the objective of identifying checkpoints in meiosis. Fusion of maturing oocytes just undergoing germinal vesicle breakdown (GVBD) induces PCC (premature chromosome condensation) but no spindle formation in immature (GV) partner oocytes. On the other hand, fusion of metaphase I (MI) oocytes containing spindles to GV oocytes induces both PCC and spindle formation in the immature partner. Thus, while molecules required for condensation are present throughout metaphase, those involved in spindle formation are absent in early M-phase. Oocytes cultured for 6 h-early metaphase I (i.e., similar to 2 h before the onset of anaphase I) - and then fused to anaphase - telophase I (A-TI) fusion partners block meiotic progression in the more advanced oocytes and induce chromatin dispersal on the spindle. By contrast, oocytes cultured for 8 h (late MI) before fusion to A-TI partners are driven into anaphase by signals from the more advanced oocytes and thereafter advance in synchrony to telophase I. When early (10 h) or late (12 h) metaphase II oocytes were fused to A-TI partners the signals generated from early MII oocytes block the anaphase to telophase I transition and induce a dispersal of A-TI chromosomes along the spindle, On the other hand, late MII oocytes respond to A-TI signals by exiting from the MII block and undergoing the A-TII transition. Moreover, the oocytes in late MI are not arrested in this stage and progress without any delay through ATI to MII when fused to metaphase II partners. The signals from the less-developed partner force the MII oocyte through A-TII to MIII. In total, these studies demonstrate that the metaphase period is divided into at least three distinct phases and that a checkpoint in late metaphase controls the progress of meiosis in mammalian oocytes. (C) 1995 Academic Press, Inc.
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页码:414 / 419
页数:6
相关论文
共 34 条
[1]  
BOSMIKICH A, 1994, J REPR FERT ABSTR SE, V13, P14
[2]  
CHANDLEY AC, 1969, MAMMALIAN DEV PRACTI, P71
[3]   INHIBITORY EFFECT OF DIBUTYRYL CAMP ON MOUSE OOCYTE MATURATION IN-VITRO [J].
CHO, WK ;
STERN, S ;
BIGGERS, JD .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1974, 187 (03) :383-386
[4]  
CHOI T, 1991, DEVELOPMENT, V113, P789
[5]   RCC1 IN THE CELL-CYCLE - THE REGULATOR OF CHROMOSOME CONDENSATION TAKES ON NEW ROLES [J].
DASSO, M .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (03) :96-101
[6]   MATURATION OF MOUSE OOCYTE IN VITRO .I. SEQUENCE AND TIMING OF NUCLEAR PROGRESSION [J].
DONAHUE, RP .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1968, 169 (02) :237-&
[7]   INHIBITORS OF DNA TOPOISOMERASE-II PREVENT CHROMATID SEPARATION IN MAMMALIAN-CELLS BUT DO NOT PREVENT EXIT FROM MITOSIS [J].
DOWNES, CS ;
MULLINGER, AM ;
JOHNSON, RT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (20) :8895-8899
[8]   ROLE OF NONHISTONE PROTEINS IN THE CHROMOSOMAL EVENTS OF MITOSIS [J].
EARNSHAW, WC ;
MACKAY, AM .
FASEB JOURNAL, 1994, 8 (12) :947-956
[9]  
EGLITIS MA, 1980, J EXP ZOOL, V213, P309, DOI 10.1002/jez.1402130222
[10]   MATURATION-INHIBITING ACTIVITY IN GROWING-MOUSE OOCYTES [J].
FULKA, J .
CELL DIFFERENTIATION, 1985, 17 (01) :45-48