AI Article Synopsis

  • The study investigates how maternal age impacts chromosome segregation errors during meiosis I in mouse oocytes.
  • Older female mice (12 months) show faster meiotic progression and altered nuclear lamina structures compared to younger females (2 months).
  • Increased activity of MPF and higher translation of related factors in aged oocytes may lead to premature meiotic processes, contributing to chromosomal errors during meiosis I.

Article Abstract

The rate of chromosome segregation errors that emerge during meiosis I in the mammalian female germ line are known to increase with maternal age; however, little is known about the underlying molecular mechanism. The objective of this study was to analyze meiotic progression of mouse oocytes in relation to maternal age. Using the mouse as a model system, we analyzed the timing of nuclear envelope breakdown and the morphology of the nuclear lamina of oocytes obtained from young (2 months old) and aged females (12 months old). Oocytes obtained from older females display a significantly faster progression through meiosis I compared to the ones obtained from younger females. Furthermore, in oocytes from aged females, lamin A/C structures exhibit rapid phosphorylation and dissociation. Additionally, we also found an increased abundance of MPF components and increased translation of factors controlling translational activity in the oocytes of aged females. In conclusion, the elevated MPF activity observed in aged female oocytes affects precocious meiotic processes that can multifactorially contribute to chromosomal errors in meiosis I.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164426PMC
http://dx.doi.org/10.3390/ijms19092841DOI Listing

Publication Analysis

Top Keywords

aged females
16
oocytes aged
12
maternal age
8
oocytes
7
females
6
aged
5
increased expression
4
expression maturation
4
maturation promoting
4
promoting factor
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!