Abstract
Purpose: The incidence of aneuploidy in eggs from women of advanced reproductive age can exceed 60 %, making the mammalian egg a unique model system to study the mechanisms of chromosome segregation errors. Methods: Here we applied a novel biophysical chromosome stretching approach to quantify mechanical stiffness of meiotic chromosomes in the mammalian egg and then documented how these properties changed in a mouse model of physiologic reproductive aging. Results: We found significant differences in chromosome micromechanics, and thus in higher order chromosome structure, coincident with advanced reproductive age, a time that is also unequivocally associated with an increase in egg aneuploidy. Conclusions: These findings have important implications for both reproductive and cancer biology where aneuploidy plays a central role in aging related disease states.
Original language | English (US) |
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Pages (from-to) | 765-769 |
Number of pages | 5 |
Journal | Journal of Assisted Reproduction and Genetics |
Volume | 32 |
Issue number | 5 |
DOIs | |
State | Published - May 1 2015 |
Funding
This work was supported by grants from the National Institutes of Health (U54HD041857 to TKW and U54HD076188, U54CA143869 and R01GM105847 to JFM) and the National Science Foundation (NSF) (MCB-1022117 and DMR-1206868 to JFM).
Keywords
- Chromosome
- Mammalian
- Meiosis
- Micromechanics
- Reproductive aging
ASJC Scopus subject areas
- Reproductive Medicine
- Genetics
- Obstetrics and Gynecology
- Developmental Biology
- Genetics(clinical)