Burgoyne P S, Baker T G
J Reprod Fertil. 1985 Nov;75(2):633-45. doi: 10.1530/jrf.0.0750633.
Postnatally, XO mice have approximately half as many oocytes as their XX sisters. A quantitative histological analysis of XO and XX ovaries throughout oogenesis (14 1/2-24 1/2 days post coitum) revealed that this oocyte deficiency in XO mice is due to excess atresia of oocytes at the late pachytene stage (19 1/2 days post coitum). Female mice heterozygous for a large X inversion (In(X)/X mice) were also found to have excess atresia at late pachytene. It was suggested that in XO mice it is the presence of an unpaired X chromosome, and in In(X)/X mice, the incompleteness of X chromosome pairing, which leads to this excess oocyte atresia. A new quantitative histological procedure which was developed for the analysis of perinatal mouse ovaries is also described.
出生后,XO小鼠的卵母细胞数量约为其XX姐妹的一半。对整个卵子发生过程(交配后14.5 - 24.5天)的XO和XX卵巢进行的定量组织学分析表明,XO小鼠的这种卵母细胞缺陷是由于粗线期晚期(交配后19.5天)卵母细胞过度闭锁所致。还发现,携带大X染色体倒位的雌性杂合小鼠(In(X)/X小鼠)在粗线期晚期也有过度闭锁现象。有人提出,在XO小鼠中,是未配对的X染色体的存在,而在In(X)/X小鼠中,是X染色体配对的不完全性,导致了这种卵母细胞过度闭锁。本文还描述了一种为分析围产期小鼠卵巢而开发的新的定量组织学方法。