Experimental evidence that changes in oocyte growth influence meiotic chromosome segregation

被引:112
作者
Hodges, CA
Ilagan, A
Jennings, D
Keri, R
Nilson, J
Hunt, PA
机构
[1] Case Western Reserve Univ, Dept Genet, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Pharmacol, Cleveland, OH 44106 USA
关键词
age-related aneuploidy; folliculogenesis; meiosis; non-disjunction;
D O I
10.1093/humrep/17.5.1171
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: It is well known that the fidelity of meiotic chromosome segregation is greatly reduced with increasing maternal age in humans. More recently, direct studies of human oocytes have demonstrated a striking age-related increase in oocytes exhibiting gross disturbances in chromosome alignment on the meiotic spindle. This abnormality, termed congression failure, has been postulated to be causally related to human non-disjunction and to result from subtle alterations in folliculogenesis that develop with advancing reproductive age. METHODS: Immunofluorescence staining, conventional cytogenetic analysis and spectral karyotyping of oocytes from mouse models were used to investigate the hypothesis that changes in the regulation of folliculogenesis induce meiotic defects. RESULTS: Mutations that affect oocyte growth were found to increase the frequency of congression failure at first meiotic metaphase. Importantly, increased congression failure was correlated with meiotic non-disjunction, suggesting a cause-and-effect relationship. CONCLUSIONS: Our findings support the hypothesis that congression failure results from disturbances in the complex interplay of signals regulating folliculogenesis and that these changes subtly alter the late stages of oocyte growth, increasing the risk of a non-disjunction error. These findings have important implications for human aneuploidy, since they suggest that it may be possible to develop prophylactic treatments for reducing the risk of age-related aneuploidy.
引用
收藏
页码:1171 / 1180
页数:10
相关论文
共 40 条
[1]   Cellular basis for paracrine regulation of ovarian follicle development [J].
Albertini, DF ;
Combelles, CMH ;
Benecchi, E ;
Carabatsos, MJ .
REPRODUCTION, 2001, 121 (05) :647-653
[2]   UNUSUAL CYTOSKELETAL AND CHROMATIN CONFIGURATIONS IN MOUSE OOCYTES THAT ARE ATYPICAL IN MEIOTIC PROGRESSION [J].
ALBERTINI, DF ;
EPPIG, JJ .
DEVELOPMENTAL GENETICS, 1995, 16 (01) :13-19
[3]   Both nuclear and cytoplasmic components are defective in oocytes of the B6.YTIR sex-reversed female mouse [J].
Amleh, A ;
Smith, L ;
Chen, HY ;
Taketo, T .
DEVELOPMENTAL BIOLOGY, 2000, 219 (02) :277-286
[4]   Live-borns from XX but not XY oocytes in the chimeric mouse ovary composed of B6.YTIR and XX cells [J].
Amleh, A ;
Taketo, T .
BIOLOGY OF REPRODUCTION, 1998, 58 (02) :574-582
[5]  
Battaglia DE, 1996, HUM REPROD, V11, P2217
[6]   Bipolar meiotic spindle formation without chromatin [J].
Brunet, S ;
Polanski, Z ;
Verlhac, MH ;
Kubiak, JZ ;
Maro, B .
CURRENT BIOLOGY, 1998, 8 (22) :1231-1234
[7]   Kinetochore fibers are not involved in the formation of the first meiotic spindle in mouse oocytes, but control the exit from the first meiotic M phase [J].
Brunet, S ;
Maria, AS ;
Guillaud, P ;
Dujardin, D ;
Kubiak, JZ ;
Maro, B .
JOURNAL OF CELL BIOLOGY, 1999, 146 (01) :1-11
[8]   Complexity in the spindle checkpoint [J].
Burke, DJ .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2000, 10 (01) :26-31
[9]   Transcriptional activity of the mouse oocyte genome: Companion granulosa cells modulate transcription and chromatin remodeling [J].
De la Fuente, R ;
Eppig, JJ .
DEVELOPMENTAL BIOLOGY, 2001, 229 (01) :224-236
[10]  
Eaker S, 2001, J CELL SCI, V114, P2953