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First published online May 23, 2008
doi: 10.1242/10.1242/dev.020560

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Selective expression of Kras^G12D in granulosa cells of the mouse ovary causes defects in follicle development and ovulation

¹ Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX77030, USA.
² Department of Applied Animal Science, Graduate School of Biosphere Science, Hiroshima University, Higashi-Hiroshima, 739-8528, Japan.
³ Breast Cancer Center, Baylor College of Medicine, Houston, TX77030, USA.
⁴ NV Organon, part of the Schering-Plough Corporation, Target Discovery Oss, Molenstraat 110, 5340 BH Oss, The Netherlands.

^* Author for correspondence (e-mail: joanner{at}bcm.edu)

Accepted 22 April 2008

Activation of the RAS family of small G-proteins is essential for follicle stimulating hormone-induced signaling events and the regulation of target genes in cultured granulosa cells. To analyze the functions of RAS protein in granulosa cells during ovarian follicular development in vivo, we generated conditional knock-in mouse models in which the granulosa cells express a constitutively active Kras^G12D. The Kras^G12D mutant mice were subfertile and exhibited signs of premature ovarian failure. The mutant ovaries contained numerous abnormal follicle-like structures that were devoid of mitotic and apoptotic cells and cells expressing granulosa cell-specific marker genes. Follicles that proceeded to the antral stage failed to ovulate and expressed reduced levels of ovulation-related genes. The human chorionic gonadotropin-stimulated phosphorylation of ERK1/2 was markedly reduced in mutant cells. Reduced ERK1/2 phosphorylation was due, in part, to increased expression of MKP3, an ERK1/2-specific phosphatase. By contrast, elevated levels of phospho-AKT were evident in granulosa cells of immature Kras^G12D mice, even in the absence of hormone treatments, and were associated with the progressive decline of FOXO1 in the abnormal follicle-like structures. Thus, inappropriate activation of KRAS in granulosa cells blocks the granulosa cell differentiation pathway, leading to the persistence of abnormal non-mitotic, non-apoptotic cells rather than tumorigenic cells. Moreover, those follicles that reach the antral stage exhibit impaired responses to hormones, leading to ovulation failure. Transient but not sustained activation of RAS in granulosa cells is therefore crucial for directing normal follicle development and initiating the ovulation process.

Key words: Ovary, Ovulation, Granulosa cell, Kras (K-ras), Signal transduction, MKP3 (DUSP6)

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