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RESEARCH PAPER / 2024-10-29

eIF4ET regulates meiotic proteome levels to enable oocyte formation and storage

Bhatia, P., Amin, R., Familiari, N. E., Yaguchi, K., Tran, V. M., Bond, A., Bukulmez, O., Woodruff, J. B.

UT Southwestern Medical Center · biorxiv

Abstract

Animals store oocytes in a dormant state for weeks to decades before ovulation. The homeostatic programs oocytes use to endure long-term storage are poorly understood. Using female nematodes as a short-lived model, we found that oocyte formation and storage required IFET-1, the conserved eIF4E-Transporter protein (eIF4ET). IFET-1 co-assembled with CAR-1 (Lsm14) to form micron-scale condensates in stored oocytes, which dissipated after oocyte activation. Depletion of IFET-1 destabilized the oocyte proteome, leading to a decline in microtubule maintenance proteins and errors in microtubule organization and meiotic spindle assembly. Deleting individual domains within IFET-1 impaired oocyte storage without affecting oocyte formation. Thus, in addition to establishing a healthy oocyte reserve in young mothers, IFET-1 ensures that correct levels of cytoskeletal proteins are maintained as oocytes age. Human eIF4ET also localized to micron-scale puncta in dormant oocytes in a reproductively healthy patient. Our results identify a role for eIF4ET in maintaining the oocyte reserve and implicate eIF4ET dysfunction as an upstream cause of embryonic aneuploidy and age-related infertility.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper investigates the role of eIF4ET in maintaining oocyte quality and storage, which is directly related to reproductive aging and age-related infertility. By identifying mechanisms that contribute to oocyte health over time, it addresses a fundamental aspect of aging in the context of fertility. However, while the findings are solid and contribute to our understanding of reproductive biology, they do not present a major breakthrough or transformative implications for the broader field of longevity research.

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