Aneuploidy in mammalian oocytes and the impact of maternal ageing

非整倍体 生物 流产 减数分裂 不育 精子 男科 老化 染色体 卵母细胞 合子 减数分裂II 遗传学 染色体分离 胚胎 怀孕 胚胎发生 医学 基因
作者
Chloe Charalambous,Alexandre Webster,Melina Schuh
出处
期刊:Nature Reviews Molecular Cell Biology [Springer Nature]
卷期号:24 (1): 27-44 被引量:32
标识
DOI:10.1038/s41580-022-00517-3
摘要

During fertilization, the egg and the sperm are supposed to contribute precisely one copy of each chromosome to the embryo. However, human eggs frequently contain an incorrect number of chromosomes - a condition termed aneuploidy, which is much more prevalent in eggs than in either sperm or in most somatic cells. In turn, aneuploidy in eggs is a leading cause of infertility, miscarriage and congenital syndromes. Aneuploidy arises as a consequence of aberrant meiosis during egg development from its progenitor cell, the oocyte. In human oocytes, chromosomes often segregate incorrectly. Chromosome segregation errors increase in women from their mid-thirties, leading to even higher levels of aneuploidy in eggs from women of advanced maternal age, ultimately causing age-related infertility. Here, we cover the two main areas that contribute to aneuploidy: (1) factors that influence the fidelity of chromosome segregation in eggs of women from all ages and (2) factors that change in response to reproductive ageing. Recent discoveries reveal new error-causing pathways and present a framework for therapeutic strategies to extend the span of female fertility.
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