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.
References
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Acknowledgments
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).
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Capsule Micromechanical properties were measured in chromosomes from the oocytes of young and old mice. Significant differences were seen in chromosomes from older mice, suggesting age-associated structural changes in chromosomes.
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Hornick, J.E., Duncan, F.E., Sun, M. et al. Age-associated alterations in the micromechanical properties of chromosomes in the mammalian egg. J Assist Reprod Genet 32, 765–769 (2015). https://doi.org/10.1007/s10815-015-0453-y
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DOI: https://doi.org/10.1007/s10815-015-0453-y