Premeiotic aster as a device to anchor the germinal vesicle to the cell surface of the presumptive animal pole in starfish oocytes

被引:30
作者
Miyazaki, A
Kamitsubo, E
Nemoto, SI
机构
[1] Ochanomizu Univ, Fac Sci, Dept Biol, Tokyo 1128610, Japan
[2] Ochanomizu Univ, Tateyama Marine Lab, Chiba 2940301, Japan
[3] Hitotsubashi Univ, Biol Lab, Kunitachi, Tokyo 1868601, Japan
关键词
aster; microtubules; centrosome; germinal vesicle; oocyte maturation; meiosis; starfish; centrifuge microscope;
D O I
10.1006/dbio.1999.9577
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The germinal vesicle (GV) of starfish oocytes stays just beneath the oocyte cortex at the presumptive animal pole during the long period of oogenesis. We subjected oocytes to a centrifugal force field to detach the GV from the cortex. The association between the cortex and the GV persisted and withstood a small amount of centrifugal acceleration at 200g. The GV was eventually separated from the cortex at 700g. The amount of acceleration sufficient for the GV separation was lowered when the oocytes were pretreated with Nocodazole and was increased by Taxol pretreatment. Observation of microtubular structures with an anti-alpha-tubulin antibody revealed the presence of a complex of spots and radiating arrays as was described by J. J. Otto and T. E. Schroeder (1984, Dev. Biol. 101, 274-281) and called the premeiotic aster. Nocodazole shortened the astral arrays, and Taxol enhanced them. These observations indicate that the premeiotic aster works as a device to hold the GV in an eccentric position just beneath the oocyte cortex. (C) 2000 Academic Press.
引用
收藏
页码:161 / 171
页数:11
相关论文
共 21 条
[1]   ORGANIZATION, NUCLEATION, AND ACETYLATION OF MICROTUBULES IN XENOPUS-LAEVIS OOCYTES - A STUDY BY CONFOCAL IMMUNOFLUORESCENCE MICROSCOPY [J].
GARD, DL .
DEVELOPMENTAL BIOLOGY, 1991, 143 (02) :346-362
[2]   Oocyte maturation in Chaetopterus pergamentaceous observed with centrifuge polarizing microscope [J].
Goda, M ;
Inoué, S ;
Knudson, RA .
BIOLOGICAL BULLETIN, 1998, 195 (02) :212-214
[3]  
GRAY J, 1927, J EXP BIOL, V5, P102
[4]   METHOD OF MICROINJECTION [J].
HIRAMOTO, Y .
EXPERIMENTAL CELL RESEARCH, 1974, 87 (02) :403-406
[5]   CENTRIFUGE MICROSCOPE AS A TOOL IN THE STUDY OF CELL MOTILITY [J].
HIRAMOTO, Y ;
KAMITSUBO, E .
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL 157, 1995, 157 :99-128
[6]   CYTOPLASMIC STREAMING IN INTERNODAL CELLS OF NITELLA UNDER CENTRIFUGAL ACCELERATION - A STUDY DONE WITH A NEWLY CONSTRUCTED CENTRIFUGE MICROSCOPE [J].
KAMITSUBO, E ;
OHASHI, Y ;
KIKUYAMA, M .
PROTOPLASMA, 1989, 152 (2-3) :148-155
[7]   ISOLATION AND IDENTIFICATION OF MEIOSIS INDUCING SUBSTANCE IN STARFISH ASTERIAS AMURENSIS [J].
KANATANI, H ;
SHIRAI, H ;
NAKANISHI, K ;
KUROKAWA, T .
NATURE, 1969, 221 (5177) :273-+
[8]  
KATO KH, 1990, DEV GROWTH DIFFER, V32, P41, DOI 10.1111/j.1440-169X.1990.00041.x
[10]  
NAKAMURA S, 1978, DEV GROWTH DIFFER, V20, P317, DOI 10.1111/j.1440-169X.1978.00317.x