DHX36 regulates antral follicle development and ovulation as a non-OSF maternal factor by maintaining oocyte homeostasis and supporting OSF delivery

Jiao, Y.-X.; Sun, F.-Y.; Bu, G.-W.; Chen, Y.-L.; Zhou, K.; Guo, B.-Y.; Deng, H.-T.; Sima, Y.-Z.; Sha, H.-Y.; Liu, S.-Y.; Sang, Y.-J.; Sun, Q.-M.; Chen, X.; Wang, H.; Ye, C.; Fan, H.-Y.

doi:10.64898/2026.08.18.745561

bioRxiv · 10.64898/2026.08.18.745561

DHX36 regulates antral follicle development and ovulation as a non-OSF maternal factor by maintaining oocyte homeostasis and supporting OSF delivery

Jiao, Y.-X.·Sun, F.-Y.·Bu, G.-W.·Chen, Y.-L.·Zhou, K.·Guo, B.-Y.·Deng, H.-T.·Sima, Y.-Z.·Sha, H.-Y.·Liu, S.-Y.·Sang, Y.-J.·Sun, Q.-M.·Chen, X.·Wang, H.·Ye, C.·Fan, H.-Y.

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Abstract

Healthy ovarian follicle development and ovulation require coordinated communication between oocytes and surrounding somatic cells. Although oocyte-secreted factors (OSFs), such as GDF-9 and BMP-15, are established regulators of this communication, the non-OSF maternal factors that support OSF delivery and signaling during late-stage follicle development remain poorly understood. Here, using an oocyte-specific Dhx36 knockout mouse model, we identify the G-quadruplex (G4) helicase DHX36 as a non-OSF maternal factor required for antral follicle development and hormone-induced ovulation. Dhx36 deficiency caused severe defects in granulosa cell proliferation and cumulus expansion, accompanied by impaired activation of SMAD2/3 and SMAD1/5/8, while ERK1/2 activation remained intact. Although the expression of major OSFs was largely unchanged, Dhx36-deficient oocytes exhibited disrupted microvilli and transzonal projections (TZPs), resulting in defective OSF delivery and impaired oocyte-cumulus communication. Proteomic, lipidomic, and ultrastructural analyses further revealed dysregulated phospholipid metabolism, membrane organization, autophagy, and organelle homeostasis, including abnormal lysosomal, mitochondrial, and endoplasmic reticulum structures. Integrative transcriptomic and proteomic analyses identified concordant downregulation of genes involved in these processes, whose promoters were enriched in potential G4 motifs. Consistently, Dhx36 deficiency was associated with reduced RNA polymerase II activity, while pharmacological G4 stabilization impaired transcription of selected genes. Together, these findings establish DHX36 as a maternal regulator that links oocyte intrinsic homeostasis to intercellular communication, suggesting that DHX36-dependent maintenance of membrane and organelle integrity is essential for OSF delivery, cumulus cell function, antral follicle development, and ovulation.

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Jiao, Y.-X., Sun, F.-Y., Bu, G.-W., Chen, Y.-L., Zhou, K., Guo, B.-Y., Deng, H.-T., Sima, Y.-Z., Sha, H.-Y., Liu, S.-Y., Sang, Y.-J., Sun, Q.-M., Chen, X., Wang, H., Ye, C., Fan, H.-Y.. 2026-08-19. DHX36 regulates antral follicle development and ovulation as a non-OSF maternal factor by maintaining oocyte homeostasis and supporting OSF delivery. https://doi.org/10.64898/2026.08.18.745561

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