Kamiguchi Y, Rosenbusch B, Sterzik K, Mikamo K
Department of Biological Sciences, Asahikawa Medical College, Japan.
Hum Genet. 1993 Jan;90(5):533-41. doi: 10.1007/BF00217454.
Two hundred and sixty-five unfertilized human metaphase II (M II) oocytes from an in vitro fertilization program were studied cytogenetically using our chromosomal technique, a gradual fixation-air drying method. Of the 265 oocytes, 185 (70%) were successfully karyotyped. There were 21 aneuploids (11.4%) consisting of 8 hyperhaploids (4.3%), 11 hypohaploids (5.9%) and 2 complex cases (1.1%). There were also 9 structural anomalies (4.9%) and 18 diploids (9.7%). In aneuploidy, the loss or gain of dyads (so-called nondisjunction) occurred more frequently than the loss or gain of monads (so-called predivision). The frequency of abnormally behaved chromosomes (segregation errors) due to nondisjunction, anaphase lag and predivision was studied among the seven chromosomal groups (A-G) and compared with the frequency expected from an equal probability of segregation errors in each of the 23 chromosomes. The observed frequency was somewhat higher than the expected frequency in groups E and G but the difference was not statistically significant in either group. These results were discussed in relation to previous studies on human M II oocyte chromosomes.
利用我们的染色体技术(一种逐步固定-空气干燥法),对来自体外受精项目的265枚未受精的人类中期II(M II)卵母细胞进行了细胞遗传学研究。在这265枚卵母细胞中,185枚(70%)成功进行了核型分析。有21枚非整倍体(11.4%),包括8枚超单倍体(4.3%)、11枚亚单倍体(5.9%)和2例复杂病例(1.1%)。还有9例结构异常(4.9%)和18枚二倍体(9.7%)。在非整倍体中,二价体的丢失或增加(所谓的不分离)比单价体的丢失或增加(所谓的提前分裂)更频繁发生。研究了七个染色体组(A-G)中由于不分离、后期延迟和提前分裂导致的染色体异常行为(分离错误)的频率,并与23条染色体中每条染色体分离错误概率相等时预期的频率进行了比较。在E组和G组中,观察到的频率略高于预期频率,但两组差异均无统计学意义。结合先前关于人类M II卵母细胞染色体的研究对这些结果进行了讨论。