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Sustained Fertility from First-wave Follicle Oocytes That Pause Their Growth

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Journal bioRxiv
Date 2024 Sep 10
PMID 39253445
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Abstract

Ovulation results from the cyclical recruitment of non-renewing, quiescent oocytes for growth. Therefore, the primordial follicles that are established during development from an oocyte encapsulated by granulosa cells are thought to comprise the lifelong ovarian reserve . However, using oocyte lineage tracing in mice, we observed that a subset of oocytes recruited for growth in the first juvenile wave remain paused for many months before continuing growth, ovulation, fertilization and development into healthy offspring. This small subset of genetically-labeled fetal oocytes, labeled with Sycp3-CreERT2, is distinguished by earlier entry and slower dynamics of meiotic prophase I. While labeled oocytes were initially found in both primordial follicles and growing follicles of the first wave, they disappeared from primordial follicles by puberty. Unexpectedly, these first-wave labeled growing oocytes persisted throughout reproductive lifespan and contributed to offspring at a steady rate beyond 12 months of age, suggesting that follicles can pause mid-growth for extended periods then successfully resume. These results challenge the conclusion from lineage tracing of granulosa cells that first-wave follicles make a limited contribution to fertility and furthermore suggest that growth-paused oocytes comprise a second and previously unrecognized ovarian reserve.

References
1.
Bergeron L, Perez G, MacDonald G, Shi L, Sun Y, Jurisicova A . Defects in regulation of apoptosis in caspase-2-deficient mice. Genes Dev. 1998; 12(9):1304-14. PMC: 316779. DOI: 10.1101/gad.12.9.1304. View

2.
Menke D, Koubova J, Page D . Sexual differentiation of germ cells in XX mouse gonads occurs in an anterior-to-posterior wave. Dev Biol. 2003; 262(2):303-12. DOI: 10.1016/s0012-1606(03)00391-9. View

3.
Li X, Li X, Schimenti J . Mouse pachytene checkpoint 2 (trip13) is required for completing meiotic recombination but not synapsis. PLoS Genet. 2007; 3(8):e130. PMC: 1941754. DOI: 10.1371/journal.pgen.0030130. View

4.
Roig I, Liebe B, Egozcue J, Cabero L, Garcia M, Scherthan H . Female-specific features of recombinational double-stranded DNA repair in relation to synapsis and telomere dynamics in human oocytes. Chromosoma. 2004; 113(1):22-33. DOI: 10.1007/s00412-004-0290-8. View

5.
Tharp M, Malki S, Bortvin A . Maximizing the ovarian reserve in mice by evading LINE-1 genotoxicity. Nat Commun. 2020; 11(1):330. PMC: 6965193. DOI: 10.1038/s41467-019-14055-8. View