首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Heterozygosity for a Bub1 mutation causes female-specific germ cell aneuploidy in mice
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Heterozygosity for a Bub1 mutation causes female-specific germ cell aneuploidy in mice

机译:Bub1突变的杂合性导致小鼠中女性特异性生殖细胞非整倍性

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摘要

Aneuploidy, the most common chromosomal abnormality at birth and the main ascertained cause of pregnancy loss in humans, originates primarily from chromosome segregation errors during oogenesis. Here, we report that heterozygosity for a mutation in the mitotic checkpoint kinase gene, Bub1, induces aneuploidy in female germ cells of mice and that the effect increases with advancing maternal age. Analysis of Bub1 heterozygous oocytes showed that aneuploidy occurred primarily during the first meiotic division and involved premature sister chromatid separation. Furthermore, aneuploidy was inherited in zygotes and resulted in the loss of embryos after implantation. The incidence of aneuploidy in zygotes was sufficient to explain the reduced litter size in matings with Bub1 heterozygous females. No effects were seen in germ cells from heterozygous males. These findings show that Bub1 dysfunction is linked to inherited aneuploidy in female germ cells and may contribute to the maternal age-related increase in aneuploidy and pregnancy loss.
机译:非整倍体是人类出生时最常见的染色体异常,也是人类妊娠流失的主要确定原因,主要来自卵子发生过程中的染色体分离错误。在这里,我们报道有丝分裂检查点激酶基因Bub1中的突变的杂合性在小鼠雌性生殖细胞中诱导非整倍性,并且随着母体年龄的增加,这种作用增加。 Bub1杂合卵母细胞的分析表明,非整倍性主要发生在第一次减数分裂期间,涉及早熟的单体染色单体分离。此外,非整倍性在受精卵中遗传,并导致植入后胚胎丢失。受精卵的非整倍性发生率足以解释与Bub1杂合雌性交配时产仔数的减少。在杂合子雄性的生殖细胞中未见作用。这些发现表明,Bub1功能障碍与女性生殖细胞中遗传的非整倍性有关,并且可能导致与母亲年龄相关的非整倍性增加和失去妊娠。

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