Bukulmez, O. | Search bioRxiv

bioRxiv2024

eIF4ET regulates meiotic proteome levels to enable oocyte formation and storage

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 stored oocyte proteome, leading to lower translation, 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 clarify the role for eIF4ET in maintaining the oocyte reserve and further support eIF4ET dysfunction as an upstream cause of embryonic aneuploidy and age-related infertility.

developmental biology↗

bioRxiv2024

Functional and Clinical Implications of Extrachromosomal Circular DNA in the Human Germline

Extrachromosomal circular DNA (eccDNA) originates from linear chromosomal DNA and can be found in various human cell types including the male germline. However, the functional effects and biogenesis mechanisms of the eccDNA in the human male germline are not well understood. Here, we developed a sequencing approach to extract eccDNA sequence information and the paired transcriptome information from the same cells. By applying this approach to human samples, we found evidence of transcriptional activities of germline eccDNAs. We also showed that patients with chronic diseases such as hypertension and diabetes had a significantly higher number of eccDNAs in the sperm than their healthy counterparts. This was, at least partly, due to an increased apoptosis signaling in the germline. Analysis of single cell RNA sequencing data of spermatogenic cells from diabetic patients vs. healthy individuals suggested that a dysregulation in the expression levels of multiple poly (ADP-ribose) polymerases may contribute to the increased amount of germline eccDNAs in diseased patients. In addition, we identified a potential horizontal transfer mechanism through which healthy sperm can take up eccDNAs from their surrounding microenvironment. Together, our results suggest that eccDNA may have functional effects on the germline, and it may serve as a non-invasive clinical biomarker for human health.

genomics↗