Investigation of effects of pregnant mare serum gonadotropin (PMSG) on the chromosomal complement of CD-1 mouse embryos

被引:23
作者
Ma, S [1 ]
Kalousek, DK [1 ]
Yuen, BH [1 ]
Moon, YS [1 ]
机构
[1] UNIV BRITISH COLUMBIA,DIV REPROD ENDOCRINOL & INFERTIL,DEPT OBSTET & GYNECOL,VANCOUVER,BC V5Z 1M9,CANADA
关键词
mouse embryos; mouse zygotes; pregnant mare serum gonadotropin; chromosomal abnormalities; triploidy;
D O I
10.1007/BF02766134
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: The objective of this study was to examine the effect of superavulatory doses of gonadotropins on the frequency of chromosomal abnormalities of mouse embryos. Methods: Chromosome analysis of 8- to 16-cell stage mouse embryos and zygotes was performed by a cytogenetic method Results: There was no significant effect of the pregnant mare serum gonadotropin (PMSG) dose on the level of aneuploidy and structural abnormalities from 8- to 16-cell-stage embryos among superovulated groups, However; a simple dose-response relationship between the PMSG dose and the incidence of polyploidy was observed, with the level of polyploidy rising from 2.9% with IO IU PMSG to 10.5% with 15 IU PMSG, In zygote stage, the proportion of polyploid embryos also increased as the dose increased, from 1.9% in 5 IU to 6.7% in 15 IU PMSG, It was observed that the extra chromosomal set in polyploidy embryos originated by both fertilization of a diploid oocyte and dispermy. Conclusions: These results indicate a dose-response relationship between the PMSG dose and the incidence of polyploidy in the CD-I mouse, Both a disturbance al maturation division and an error at fertilization were the cause of polyploidy.
引用
收藏
页码:162 / 169
页数:8
相关论文
共 24 条
[1]  
*AM FERT SOC SOC A, 1994, 1992 RES GEN AM FERT, V62, P1121
[2]   BLASTOMERE KARYOTYPING AND TRANSFER OF CHROMOSOMALLY SELECTED EMBRYOS - IMPLICATIONS FOR THE PRODUCTION OF SPECIFIC ANIMAL-MODELS AND HUMAN PRENATAL-DIAGNOSIS [J].
BACCHUS, C ;
BUSELMAIER, W .
HUMAN GENETICS, 1988, 80 (04) :333-336
[3]   EFFECT OF THE DEGREE OF MATURATION OF MOUSE OOCYTES AT FERTILIZATION - A SOURCE OF CHROMOSOME IMBALANCE [J].
BADENAS, J ;
SANTALO, J ;
CALAFELL, JM ;
ESTOP, AM ;
EGOZCUE, J .
GAMETE RESEARCH, 1989, 24 (02) :205-218
[4]  
BOUE JG, 1973, LANCET, V1, P679
[5]   DIGYNIC TRIPLOIDY AFTER SUPEROVULATION [J].
CHANG, MC .
NATURE, 1977, 266 (5600) :382-383
[6]  
EVANS G, 1984, J REPROD FERTIL, V70, P131, DOI 10.1530/jrf.0.0700131
[7]  
FUJIMOTO S, 1974, J REPROD FERTIL, V40, P177, DOI 10.1530/jrf.0.0400177
[8]  
Hansmann I., 1983, Cytogenetics of the mammalian X chromosome. Part A. Basic mechanisms of X chromosome behavior., P131
[9]   INCIDENCE OF NONDISJUNCTION IN MOUSE OOCYTES [J].
HANSMANN, I ;
ELNAHASS, E .
CYTOGENETICS AND CELL GENETICS, 1979, 24 (02) :115-121
[10]  
HANSMANN I, 1980, EUR J CELL BIOL, V22, P24