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Updated: Aug 29, 2026

Whole Ovary Immunofluorescence, Clearing, and Multiphoton Microscopy for Quantitative 3D Analysis of the Developing Ovarian Reserve in Mouse
Published on: September 3, 2021
Small nuclear RING finger protein expression during gonad development: regulation by gonadotropins and estrogen in
Sirpa J Hirvonen-Santti1, Venkataraman Sriraman, Mikko Anttonen
1Biomedicum Helsinki, Institute of Biomedicine (Physiology), University of Helsinki, P.O. Box 63, FIN-00014 Helsinki, Finland.
Abstract:
Small nuclear RING finger protein (SNURF/RNF4) is a steroid receptor coregulator that is down-regulated in testicular germ cell cancer. In this work, we examined SNURF expression during murine fetal gonad development and postnatal ovarian folliculogenesis by in situ hybridization and immunohistochemical staining. SNURF mRNA was detectable in gonads of both sexes from embryonic 10.5 days post conception onward. SNURF protein localized to gonocytes and somatic Leydig and Sertoli cells of fetal testis and in oogonia and supporting cells of fetal ovary. In murine postnatal ovary, SNURF mRNA and protein were expressed throughout folliculogenesis, peaking in the oocytes of preantral follicles. Lower amounts of SNURF mRNA and protein were also present in granulosa cells of secondary, antral, and preovulatory follicles and in luteal glands. Exposure of immature female mice and rats to gonadotropin from pregnant mare serum and human chorionic gonadotropin did not change dramatically SNURF mRNA levels in ovary. SNURF mRNA expression was increased in ovaries of immature mice treated with diethylstilbestrol, an effect that was blocked by the pure antiestrogen ICI 182,780. SNURF protein was constitutively expressed in oocytes of hypophysectomized rats, and its content was augmented by estradiol in granulosa cells. In granulosa cell culture, SNURF mRNA accumulation was transiently increased by treatment with the LH agonists phorbol myristate and forskolin at 4 h after treatment and at 48 h in differentiated cells expressing markers of the preovulatory phenotype. These results suggest a role for SNURF in fetal germ cell development as well as in oocyte and granulosa cell maturation in an estrogen- and gonadotropin-regulated fashion.
Insights
Small nuclear RING finger protein (SNURF) plays a role in fetal germ cell development and ovarian maturation. Its expression is regulated by estrogen and gonadotropins, suggesting involvement in reproductive processes.
Area of Science:
- Reproductive Biology
- Molecular Endocrinology
- Developmental Biology
Background:
- Small nuclear RING finger protein (SNURF/RNF4) is a steroid receptor coregulator.
- SNURF is notably down-regulated in testicular germ cell cancer.
Purpose of the Study:
- To investigate SNURF expression during murine fetal gonad development.
- To examine SNURF's role in postnatal ovarian folliculogenesis.
Main Methods:
- In situ hybridization and immunohistochemical staining were employed.
- Analysis of SNURF expression in fetal and postnatal murine ovaries and testes.
- Hormonal and antiestrogen treatments in immature female mice and rats.
Main Results:
- SNURF mRNA and protein were detected in gonads of both sexes from embryonic day 10.5.
- SNURF expression peaked in oocytes of preantral follicles and was present in granulosa cells and luteal glands.
- Estrogen significantly increased SNURF mRNA, an effect blocked by antiestrogen; gonadotropins had minimal impact.
Conclusions:
- SNURF is involved in fetal germ cell development.
- SNURF plays a role in oocyte and granulosa cell maturation.
- SNURF expression is regulated by estrogen and gonadotropins during ovarian development.
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