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
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI