For Manuscript Submission, Check or Review Login please go to Submission Websites List.
For the academic login, please select your country in the dropdown list. You will be redirected to verify your credentials.
Genetic Control of Ovarian DevelopmentTevosian S.G.
Department of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, Fla., USA Corresponding Author
Sergei G. Tevosian
Department of Physiological Sciences, College of Veterinary Medicine
University of Florida, 1333 Central Drive
Gainesville, FL 32601 (USA)
Tel. +1 352 294 4364, E-Mail firstname.lastname@example.org
During embryonic development, ovarian somatic cells embark on a course that is separate from male somatic cells and from indifferent precursor cells. While the former aspect of ovarian development is well known, the latter has not received much attention until recently. This review attempts to integrate the most recent work regarding the differentiation of ovarian somatic cells. The discussion of the parallel development of the testis is limited to the key differences only. Similarly, germ cell development will be introduced only inasmuch as it becomes necessary to draw attention to a particular aspect of the somatic component differentiation. Finally, while postnatal ovarian development and folliculogenesis undoubtedly provide the ultimate morphological and functional fitness tests for the ovarian somatic cells, postnatal phenotypes will be only referred to when they have already been connected to genes that are expressed during embryogenesis.
© 2012 S. Karger AG, Basel
Sexual development in most mammals is genetically determined by the inheritance of the father’s Y chromosome by male, but not female, offspring at fertilization. Despite this initial fundamental and irreversible commitment, the sex determination program remains latent, and male (XY) and female (XX) embryos are morphologically indistinguishable during their early development. In both sexes, the bipotential (indifferent) gonads arise from the urogenital ridges that appear on the surface of the mesonephroi, which are bilateral rudimentary nephric primordia that lie laterally to the differentiating gonad. At a specific developmental stage, the male and the female pathways diverge: the XY gonadal anlagen differentiate into testes and the XX anlagen form ovaries. This sex determination step in male mammals is initiated by Sry (sex-determining region of chromosome Y), the Y chromosome-linked testis-determining gene. Triggered by SRY, the formation of testes from the bipotential embryonic gonad, rather than ovaries, is considered to be the decisive step for subsequent male sexual development [reviewed in Swain and Lovell-Badge, 1999; Capel, 2000; Wilhelm et al., 2007; Combes et al., 2010]. Given that the majority of the functional genetic data has been obtained through gene manipulation in mice, they will be used as the main reference species for further discussion. Nevertheless, studies of disorders of sexual development (DSD) in humans and in other species (e.g. goat) have been very valuable towards our understanding of ovarian development, and these will be considered as well.
The discovery that testis determination in mammals is contingent on the presence of the Y chromosome provided further support for a model where the process of ovarian differentiation occurs by default, unless it is redirected by the Y chromosome to make a testis [Jost, 1972; Burgoyne, 1988; Goodfellow and Darling, 1988]. The isolation of Sry [Gubbay et al., 1990; Sinclair et al., 1990; Koopman et al., 1991] was the seminal step that provided a solid genetic foundation for the subsequent 20 years of molecular analysis of male sexual development. The parsimonious concept of a single switch that alone controls cell fate was affirmed in testis development, where a sole gene (i.e. Sry or later its direct target Sox9) is sufficient for sex determination [Koopman et al., 1991; Bishop et al., 1999; Vidal et al., 2001; Sekido and Lovell-Badge, 2008]. Similarly, in the absence of SRY or SOX9 function, the bipotential gonad develops as an ovary [Koopman et al., 1991; Chaboissier et al., 2004; Barrionuevo et al., 2006].
The cases of XY sex reversal in the presence of Sry (XY females, e.g. B6-YPOS) [Eicher et al., 1982] or SRY-negative XX sex reversal (XX males) could formally be explained within the framework of the ‘default’ pathway. However, an alternative mechanism that would allow for a more prominent role for the female-specific genes appeared at least equally attractive. Not surprisingly, the ‘master gene’ paradigm influenced the quest for a similar omnipotent determinant of ovarian destiny. It was proposed, variously, that such a hypothetical gene could either independently initiate ovarian development (the concept of the ‘ovarian determinant’, pioneered by Eva Eicher) [Eicher and Washburn, 1983; Washburn and Eicher, 1983; Eicher and Washburn, 1986] or suppress the default genetic pathways leading to testis formation (dubbed ‘factor Z’) [McElreavey et al., 1993]. In this latter model, the antagonistic nature of male and female determinants (as well as their downstream targets) is explicitly emphasized [Ottolenghi et al., 2007a]. To date, the precise genetic mechanism of sexual development is still enigmatic for mammalian females. While no complete XX sex reversal has been described in recessive mouse models, the possibility remains that a single, yet unidentified, gene controls ovarian sex determination. In recent years, however, the notion of an ovarian counterpart to Sry gave way to a less stringent hypothesis, where more than one gene is involved in the initial commitment to the ovarian fate. Several combinations have been postulated and will be discussed below. While the argument for a collective hypothesis of ovarian determination appears persuasive, it remains to be proven conclusively, and the precise gene combination that unlocks the ovarian fate remains unknown.
Currently, the notion that the embryonic ovary engages in active gene regulation appears almost mundane. However, sexually dimorphic gene expression in the somatic cells of the embryonic ovary has only been identified fairly recently [Menke and Page, 2002]. It is widely believed that the genetic programs of male and female development are closely intertwined and that the 2 alternative fates are likely to be determined by antagonistic activities. Experimental evidence suggests that the process of dimorphic gonadal development is initiated in a limited number of cells by sex-specific transcription factors and is then expanded by extracellular, non-cell-autonomous signals that promote one developmental program while suppressing the other (fig. 1) [Palmer and Burgoyne, 1991; Goodfellow and Lovell, 1993; Brennan and Capel, 2004; Wilhelm et al., 2005; Capel, 2006; Kim and Capel, 2006; Kim Y et al., 2006].
The 2 main roles of the ovary are the production of steroid hormones and the generation of mature oocytes [reviewed in Edson et al., 2009; Richards and Pangas, 2010]. The follicle is the functional unit of the adult ovary; it is comprised of a mature oocyte that is surrounded by supporting granulosa cells (the female counterpart of Sertoli cells) and the steroidogenic theca cells (the female counterpart of adult Leydig cells). The formation of testis cords in mice refers to the stereotypic rearrangement of the somatic Sertoli cells to enclose the gonocytes at embryonic day (E) 12.5. This extensive structural reorganization clearly demarcates the commencement of male differentiation. Unlike this comprehensive transformation of the male gonad, the female organ does not undergo dramatic morphological changes until close to birth. One should not infer, however, that the embryonic ovary remains dormant. At the molecular and cellular level, it has long been known that the embryonic ovary engages in robust dimorphic activity, with ovarian germ cells (the oogonia) beginning to enter meiosis at E12.5 [reviewed in Byskov, 1986; McLaren and Southee, 1997; Byskov and Nielsen, 2003]. In addition, confocal analysis shows that the poorly differentiated XX gonad undergoes some remodeling between E13.5 and E15.5, when the primordial germ cells develop as interconnected cysts/clusters that are linked by cytoplasmic bridges [Gondos and Zamboni, 1969; Pepling and Spradling, 1998]. While segmentation into the cortex and medulla is not morphologically apparent in mice during embryogenesis, these areas are definable by gene expression as early as E12.5. Specifically, cells in the sub-coelomic (cortex) area express Bmp2 (see below), while the central (medulla) area expresses markers normally associated with pre-granulosa cells: Wnt4, Fst, and Foxl2.
The granulosa cells of the developing ovary are somatic cells that are derived from the same progenitor population as the Sertoli cells of the testis [Burgoyne et al., 1988; McLaren, 1991; Albrecht and Eicher, 2001]. In agreement with their pre-Sertoli/pre-granulosa status, these cells residing in the medullar area also express the Sry-Egfp transgene (Tg92) [Albrecht and Eicher, 2001]. Specifically, Albrecht and Eicher  generated a transgenic mouse line Tg92 in which EGFP expression was driven by proximal ∼8 kb of Sry promoter elements (Sry-Egfp). The EGFP expression pattern in XY transgenic embryos resembled endogenous Sry expression. In addition, EGFP expression from the transgene was detected in a subset of somatic cells in the medullar region of the XX gonad, indicating that both testis and ovary contained primed cell populations capable of activating the Sry gene promoter. The authors proposed that a Sry-Egfp-expressing population had acquired the competence to differentiate into the supporting cell lineage from which both Sertoli and granulosa cells are derived. In contrast to the XY cells that down-regulate Sry-Egfp concomitantly with the endogenous Sry expression at E12.5, the XX cells retained reporter activity after the time of birth. Similar results were obtained in a lineage mapping experiment using a 9.9-kb Sry-promoter driven Cre line, with activated reporter activity still detectable in the ovary 2 weeks after birth and restricted to a subset of descendant granulosa cells [Ito et al., 2006].
A recent work re-evaluated the commitment of XX Sry-Egfp-expressing cells in Tg92 animals to granulosa cell fate and demonstrated that in E12.5–E13.5 embryos these cells are also positive for the granulosa cell marker, FOXL2 [Mork et al., 2011]. While this observation further ascertained pre-granulosa status of the XX Sry-expressing cells, it was also noted that EGFP-positive and FOXL2-positive populations in the ovary did not completely overlap. This suggested the heterogeneous nature of embryonic cells that gave rise to pre-granulosa lineage.
The relationship between these domains of embryonic gene expression and the cortex/medulla domains of the adult ovary is not yet clear. However, in both aforementioned experiments that capitalized on the opportune competence of granulosa cell precursors to express Sry, only a small fraction of granulosa cells retained detectable EGFP expression after the time of birth. Capel and colleagues took these observations further by showing that contribution of the embryonic bipotential supporting cell precursors to postnatal ovary was limited [Mork et al., 2011]. The rare descendants of embryonic precursors were scattered among non-labeled granulosa cells and confined to a specific subset of medullar follicles that began to grow immediately after birth. Using a tamoxifen-inducible Foxl2-Cre transgenic line, the authors traced the origin of the precursor cells to the proliferative ovarian surface epithelium. In contrast, granulosa cells in the cortical primordial follicles (that ultimately constitute the adult follicular supply) appeared instead to derive from the surface epithelium between the time of birth and postnatal day (P) 7. These observations introduce a previously underappreciated possibility that the majority of granulosa cells in the adult ovary originate from cells other than their embryonic counterpart. It is important to keep the perspective that different floxed loci exhibit differential susceptibility to Cre recombination which may have a substantial impact on the outcome of fate mapping experiments [Vooijs et al., 2001; Ma et al., 2008]. It will be interesting to explore this tantalizing hypothesis further (for example by using inducible Foxl2-driven Cre line with reporter strains other than R26RLacZ) [Novak et al., 2000; Vooijs et al., 2001; Ma et al., 2008].
In contrast to female germ cells, the pre-granulosa and other somatic populations of the embryonic ovary have not received sufficient attention until recently. This relative neglect is normally attributed to a lack of discernable elements when compared to the multitude of events that are characteristic of early testis development such as cord formation, robust cellular proliferation, steroidogenesis, and prominent vascular development [reviewed in Brennan and Capel, 2004; Munger et al., 2009]. While the validity of this assumption is debatable, it is indisputable that a major breakthrough in identifying female-specific gene expression as early as E11.5 became possible with the advent of differential RNA expression screening, particularly microarray technology [Menke et al., 2003; Yao et al., 2004; Jorgensen and Gao, 2005; Nef et al., 2005; Small et al., 2005; Beverdam and Koopman, 2006; Cederroth et al., 2007; Lee et al., 2008].
Gata4/6 and Fog2
The transcription factors of the GATA family (GATA binding proteins 4 and 6) and their co-factor FOG2 (Zfpm2, zinc finger protein, multitype 2) have been implicated as key drivers of multiple developmental processes [Molkentin, 2000; Patient and McGhee, 2002; Morceau et al., 2004; Viger et al., 2008]. Ovarian sexual development is dramatically affected by the loss of the GATA4-FOG2 interaction. One of the roles of the GATA4-FOG2 complex is to serve as a repressor for the Dkk1 gene that encodes a secreted inhibitor of canonical β-catenin signaling (see below) [Manuylov et al., 2008]. The role of the GATA family proteins in sex determination and gonadal differentiation has recently been the subject of an extensive review [Zaytouni et al., 2011] and hence will not be duplicated here.
Foxl2 (Forkhead Box L2)
The forkhead transcription factor Foxl2 can be detected in the developing XX gonad in mice as early as E11.5 [Wilhelm et al., 2009], making it one of the earliest markers of a commitment to granulosa cell fate in the supporting cell lineage. Foxl2 expression continues throughout the subsequent ovarian development in somatic granulosa and theca cells of all the follicular stages [Schmidt et al., 2004]. FOXL2 was briefly considered to be the long-sought-after female-determining factor because of its association with female-to-male sex reversal in polled intersex syndrome goats [Pailhoux et al., 2001] and its conserved ovarian expression pattern in several vertebrates [Loffler et al., 2003; Wang et al., 2004]. However, subsequent studies did not support this seminal role for FOXL2 in early ovary organogenesis, at least in humans and in mice. Human patients carrying mutations in the FOXL2 gene display blepharophimosis, ptosis and epicanthus inversus syndrome, an autosomal disease characterized by eyelid defects and premature ovarian failure in females, but no sex reversal [Townes and Muechler, 1979; Crisponi et al., 2001; Pailhoux et al., 2001]. Similarly, ablation of the Foxl2 gene in mice leads to a block in the squamous-to-cuboidal transition of the postnatal granulosa cells. The impaired differentiation of Foxl2–/– granulosa cells leads to a premature depletion of the primordial follicle pool and infertility. In contrast to the profoundly disabled follicular development, the embryonic appearance of the ovary in Foxl2 null females is unremarkable, with no indications of cord formation or other fundamentals of testis development [Schmidt et al., 2004; Uda et al., 2004]. Ectopic expression of Foxl2 in XY transgenic mice impaired the differentiation of the testis cords [Ottolenghi et al., 2007b]; this experiment demonstrated the anti-testis properties of Foxl2 but provided no evidence for concomitant ovarian differentiation. While the preponderance of data did not support the crowning of FOXL2 as the sole ovarian determinant, subsequent research confirmed the pivotal role of this transcription factor in maintaining ovarian identity as described below [for recent reviews, see Schlessinger et al., 2010; Uhlenhaut and Treier, 2011].
Wnt4 (Wingless-Related MMTV Integration Site 4)
WNT4 belongs to a family of 19 secreted proteins that play key roles during development, including embryonic organogenesis, the generation of cell polarity, and cell differentiation in vertebrates. WNT proteins are known to activate 3 discrete pathways upon binding to different WNT receptors: the canonical Wnt/β-catenin cascade, the non-canonical planar cell polarity (PCP) pathway, and the Wnt/Ca2+ pathway [reviewed in Katoh, 2005; Kohn and Moon, 2005; Huang and He, 2008]. The canonical Wnt/β-catenin pathway is central to the embryonic development of the mammalian ovary and will be considered in greater detail in the following section. At the bipotential stage, low levels of Wnt4 expression are present in both XY and XX gonads. This expression becomes female-specific by E12.5. Female embryos lacking functional WNT4 exhibit several notable defects in their sexual development, including a rounded testis-like shape of the gonad, the emergence of androgen-producing cells, the appearance of male-specific structures at birth, and the loss of female germ cells (oogonia) beginning at E15.5 [Vainio et al., 1999]. Further work highlighted additional features of Wnt4 deletion and firmly put this gene in the center of the genetic network regulating ovarian development. In the female, WNT4 prevents the formation of a male-specific coelomic blood vessel and the production of steroids [Jeays-Ward et al., 2003; Jordan et al., 2003]. A duplication of WNT4 in an XY sex-reversed patient has been described [Jordan et al., 2001]. Similarly, a heterozygous mutation in WNT4 results in an excess of androgen and an absence of the uterus (an atypical Mayer-Rokitansky-Küster-Hauser-like syndrome) [Biason-Lauber et al., 2004, 2007], while a homozygous loss of function mutation leads to a severe SERKAL (female sex reversal and dysgenesis of kidneys, adrenals, and lungs) syndrome (fetal lethality and testes or ovotestes in XX fetuses) [Mandel et al., 2008]. It is of note that the histological appearance of the testes in a 19-week-old 46,XX fetus with a homozygous WNT4 mutation was characterized as ‘normal-looking’ [Mandel et al., 2008], suggesting that (similarly to Rspo1/RSPO1, see below) the degree of sex-reversal could be more complete in humans than in Wnt4 null mice [Vainio et al., 1999].
The work of McMahon and colleagues identified the role of WNT4 in the ovary in the late 90s [Stark et al., 1994; Vainio et al., 1999]. One might think that establishing the mechanistic connection to the canonical β-catenin pathway in the ovary was straightforward from that point on. However, it took almost a decade before this connection was established. One can only speculate why it took so long for such a connection to be made; perhaps an emphasis was simply not placed on the study of ovarian development at the time. Wnt4 deletion was among the first mouse models that primarily affected the somatic cells of the embryonic ovary, where few, if any, of the genetic causes of morphological features were known at the time. Hence, in their analysis of the Wnt4 mutant phenotype, the authors were constrained by a rather limited armamentarium at their disposal [Vainio et al., 1999]. WNT4 loss resulted neither in the expression of Sertoli cell markers (e.g. Sox9, Dhh (Desert hedgehog), Amh (Anti-Müllerian hormone/Müllerian-inhibiting substance)) nor in morphologically identifiable sex cords in embryonic XX gonads. This indicated that the ovaries of Wnt4 mutants had not undergone a primary sex reversal leading to Sertoli cell development. However, other ovarian-specific genes were not known, and therefore one could not tell whether their expression was compromised. An observation that initially appeared to support a direct role for Wnt4 in ovarian development was ectopic steroidogenic gene expression in Wnt4 null ovaries. This led to the hypothesis that ovarian Wnt4 normally functions to suppress the development of Leydig cells [Vainio et al., 1999]. However, the follow-up analysis suggested that, rather than regulating a gonad-autonomous steroidogenic cell fate, WNT4 controls the migration of the endothelial and steroidogenic precursor cells [Hatano et al., 1996] into the ovary [Heikkila et al., 2002; Jeays-Ward et al., 2003]. Transgenic misexpression of Wnt4 in the embryonic testis did not suppress Leydig cell differentiation [Jeays-Ward et al., 2003]. Additionally, germ cells in XX Wnt4 mutant gonads were entering meiosis normally [Yao et al., 2004], indicating that the deletion of Wnt4 does not impair or reverse this essential embryonic function. In light of these findings, the commanding position for Wnt4 in ovarian development suddenly appeared less certain.
Uncovering the requirement for Wnt4 in antagonizing the male expression program constituted an important next step in the mechanistic understanding of ovarian development [Kim Y et al., 2006a]. Before the 2 opposing sex fates are established, the proteins that control them are already detectable in the mutually exclusive domains of the gonadal anlage, but in insufficient amounts to launch the programs. In the absence of WNT4, a male-promoting growth factor, fibroblast growth factor 9 (FGF9) becomes ectopically activated [Kim Y et al., 2006b]. FGF9 leads to a dramatic, but transient, spike in SOX9 expression in the E11.5–E12.0 XX Wnt4 null gonad. Similarly, loss of Fgf9 expression results in the ectopic up-regulation of Wnt4 in the XY gonad. These findings provided the foundation for a ‘tug-of-war’ hypothesis, where the competition between 2 mutually antagonistic signals, namely Fgf9 (induced by Sry/Sox9) in the male and Wnt4 in the female, determines the outcome of the battle of the sexes. In the absence of Sry/Sox9/Fgf9 expression, an increase in Wnt4 activity becomes sufficient for switching on the female pathway and for repressing testis development [reviewed in Kim and Capel, 2006].
Fst and Bmp2
Another important step in strengthening the commanding position for Wnt4 was the elucidation of the genetic interactions between Wnt4, Bmp2 (bone morphogenic protein), and Fst (follistatin). An astute observation by Capel and colleagues of coelomic vessel formation in XX Fst–/– embryos laid the foundation for the understanding of the epistatic relationship between these recently emerged ovarian-enriched genes [Yao et al., 2004]. Fst was one of the first genes that was isolated specifically based on its preferential expression in the embryonic ovary versus the testis [Menke and Page, 2002]. Fst expression was found to be absent in Wnt4 null embryonic gonads, while Wnt4 was expressed normally in Fst–/– gonads. This observation placed Wnt4 upstream of Fst. Because the deletion of both genes led to a similar loss of germ cells, it was proposed that Fst acts as a downstream effector of Wnt4 to promote germ cell survival [Yao et al., 2004]. This work also documented the dimorphic (ovary-biased) expression of another gene, Bmp2, which is restricted to the layer of cells just beneath the coelomic layer at E12.5. The expression pattern of these genes positions Wnt4 at the top of the ovarian genetic cascade, as Bmp2 expression is also absent in Wnt4 null gonads but does not require Fst. Recently, it was suggested that while WNT4 is required to activate Fst expression, its maintenance depends on the cooperation between BMP2 and FOXL2 [Kashimada et al., 2011]. FST is expressed as multiple isoforms, and the absence of separate isoforms is sufficient to cause fertility defects in mice [Kimura et al., 2010, 2011]. Bmp2 knockout leads to early embryonic lethality [Zhang and Bradley, 1996]; the function of Bmp2 in ovarian development remains to be explored.
The canonical Wnt/β-catenin pathway is the best-understood signaling sequence initiated by WNT proteins. It begins with a WNT ligand binding to a complex that is composed of a membrane-associated Frizzled (Fz) and an LDL-related receptor protein 5 (LRP5) or LRP6 co-receptor. This binding triggers a cascade of events culminating in the disassembly of the cytoplasmic β-catenin destruction complex that, in the absence of WNT, binds β-catenin and mediates its phosphorylation and subsequent degradation. Once free, β-catenin translocates into the cell nucleus where it participates in transcriptional regulation in partnership with the TCF/LEF family of transcription factors [for recent reviews, see Clevers, 2006; Grigoryan et al., 2008; van Amerongen and Nusse, 2009]. The function of this pathway in ovarian regulation has been recently reviewed [Zaytouni et al., 2011].
The activity of the canonical Wnt/β-catenin pathway is modulated by several regulatory proteins that interact with either WNT molecules themselves or with their receptors [reviewed in Kikuchi et al., 2007]. These accessory proteins can serve to either enhance or suppress WNT signaling. DKK1, a member of the Dickkopf family of secreted proteins, acts as a designated antagonist of WNT-dependent activation. DKK1 inhibition of the canonical Wnt pathway is achieved through its ability to bind with high affinity to the LRP5 or LRP6 co-receptors, which prevents the formation of productive Fz-LRP5/6 receptor complexes [Bafico et al., 2001; Mao et al., 2001; Semenov et al., 2001]. In some settings, DKK1 appears to block Wnt signaling by simultaneously binding to LRP6 and to receptors of the Kremen family, thus inducing the internalization of the LRP6-Kremen complex [Mao et al., 2002], although this mechanism is unlikely to be universal. No other function for DKK1 other than its role as a Wnt pathway inhibitor has been described.
In contrast, R-spondins (RSPOs) represent a family of soluble proteins that act as co-activators of the canonical Wnt signaling pathway [Kim KA et al., 2006]. The biochemical mechanism of WNT modulation by RSPO proteins remains to be understood. It has been proposed that RSPOs activate Wnt/β-catenin signaling by directly interacting with the WNT proteins, by facilitating the formation of the Fz/LRP receptor complex, or by directly binding to LRP receptors [Kazanskaya et al., 2004; Nam et al., 2006; Wei et al., 2007]. It has also been suggested that RSPOs could act through an alternative WNT-independent pathway to induce β-catenin activation [Kim et al., 2005; Gibbons et al., 2007]. Yet another study proposed that RSPO1 could be regulating Wnt signaling by preventing the DKK1/Kremen-mediated internalization of the LRP5/6 co-receptor [Binnerts et al., 2007]. Given the low levels of DKK1 expression in many tissues where RSPO1 is present, this last scenario could be uncommon. A mechanism that is likely to be more general postulates that RSPO proteins augment WNT activity by serving as ligands to the recently characterized LGR4/5/6 receptors [Carmon et al., 2011; de Lau et al., 2011; Glinka et al., 2011]. The resulting RSPO-LGR4/5/6 complexes are thought to promote a more efficient sequestration of the GSK3 enzyme that plays a key role in β-catenin inactivation [Taelman et al., 2010].
The connection between RSPO1 and ovarian development first emerged through studies of a complete sex reversal in human XX patients. These patients developed testes and were harboring either a single-nucleotide insertion or a deletion in the RSPO1 gene [Vernole et al., 2000; Parma et al., 2006]. Rspo1 ovarian expression has been documented in several vertebrate species, prompting the suggestion that its ovary-determining role is highly conserved [Parma et al., 2006; Smith et al., 2008]. A homozygous splice donor site mutation in the RSPO1 gene resulted in an XX patient having both testicular and ovarian structures [Tomaselli et al., 2008]. Gene targeting in mice confirmed the role of the Rspo1 gene in ovarian development [Chassot et al., 2008; Tomizuka et al., 2008]. XX Rspo1–/– animals developed ectopic coelomic vessels, persisting Wolffian ducts, and virilized external genitalia. Importantly, while ovarian development in these mice was dramatically impaired, a complete sex reversal was not observed. XX Rspo1–/– animals remained phenotypically female and developed functional follicles, with some retaining their fertility [Chassot et al., 2008; Tomizuka et al., 2008]. Overexpression of RSPO1 (goat RSPO1) did not interfere with male development, suggesting that RSPO1 gain-of-function is not sufficient to result in a sex reversal [Buscara et al., 2009]. While these experiments did not confirm a commanding role for RSPO1 in the ovarian developmental program, exploring the mechanism of RSPO1 function in ovarian differentiation was gratifying. In this respect, Chassot and colleagues  were the first to compellingly demonstrate the presence of the active canonical Wnt/β-catenin pathway in the ovary using the Axin2LacZ reporter strain and to examine the epistatic relationship between Rspo1, Wnt4, and β-catenin (see below).
While RSPO1 also did not quite fulfill its advanced billing as a universal ovarian-determining factor, studies in Rspo1-/- mice provided incontrovertible evidence that the canonical Wnt/β-catenin pathway is operating in the embryonic ovary [Chassot et al., 2008]. An identified role for another member of the Wnt pathway that is specifically implicated in canonical (vs. other) signaling intensified the search for evidence of the pathway’s role in ovarian differentiation. Once again, in hindsight, the finding that Fst expression was absent in XX Wnt4–/– gonads [Yao et al., 2004] made the next step (the connection to canonical β-catenin signaling) all but trivial – even without the ‘bonus’ Rspo1 hint. Indeed, in cultured cells the regulation of a Fst promoter by canonical β-catenin signaling has long been documented [Miyanaga and Shimasaki, 1993]. Moreover, mutating the putative TCF binding site in the Fst promoter led to a loss of response to the ‘classical’ canonical WNT3a ligand [Willert et al., 2002]. Given these quite explicit clues, one has to wonder why it took a few extra years before the Wnt/β-catenin pathway’s involvement as a key ovarian pathway came to light, as described below. Again, one can only speculate, but it is possible that the first barrier was our incomplete understanding of Wnt signaling just a few years ago [e.g. Bernard and Harley, 2007]. It was believed that Wnt4 belonged to a group of so-called ‘non-canonical’ Wnts that do not engage β-catenin [e.g. Shimizu et al., 1997]. Several years later, it became clear that the ability to engage a specific Wnt pathway is not an intrinsic property of a Wnt ligand, but rather any WNT molecule can activate β-catenin, provided an appropriate receptor is available [Mikels and Nusse, 2006]. Yet another obstacle was the limited ability to effectively monitor the presence of canonical β-catenin signaling in the developing gonad. The TOPGAL LacZ cassette (the first Wnt/β-catenin reporter that immediately became prevalent for inspecting the sites of β-catenin signaling in mice) [DasGupta and Fuchs, 1999] was inactive in developing gonads [Tevosian and Manuylov, 2008]. The strain that ultimately turned out to be informative for scoring the activity of the Wnt/β-catenin pathway in the gonadal somatic cells, the Axin2LacZ strain [Yu et al., 2005], was not widely available until 2007. This more sensitive reporter unequivocally reveals the presence of canonical signaling in the somatic cells of developing ovaries but not in the testes [Chassot et al., 2008; Manuylov et al., 2008; Tevosian and Manuylov, 2008].
The genetic and biochemical evidence presented above suggested that both RSPO1 and WNT4 might ultimately exert their actions through the intracellular regulator, β-catenin [Mizusaki et al., 2003; Kim KA et al., 2006; Park et al., 2007; Chassot et al., 2008; Manuylov et al., 2008]. This set the stage for directly querying the involvement of β-catenin in ovarian development. Loss-of-function studies produced compelling evidence connecting the canonical Wnt pathway to ovarian differentiation [Manuylov et al., 2008; Liu et al., 2009]. A Cre recombinase, driven by the regulatory elements of the steroidogenic factor 1 (SF1)-encoding gene [Bingham et al., 2006], was an essential tool in these studies. To examine the role of β-catenin in ovarian development, a floxed β-catenin gene [Brault et al., 2001] was specifically inactivated in SF1-positive ovarian somatic cells. The XX Sf1Cre; β-cateninflox/flox mutants exhibited a comprehensive block in the embryonic ovarian gene expression program, similarly to the ones previously reported for Wnt4 and Rspo1 knockouts [Manuylov et al., 2008; Liu et al., 2009]. Likewise, when β-catenin is reintroduced in the absence of either Rspo1 or Wnt4, it rescues normal ovarian development [Chassot et al., 2008; Liu et al., 2009], suggesting that β-catenin is their common and main effector. While Wnt4 expression is lost in ovaries lacking β-catenin, Rspo1 expression remains unchanged, indicating that RSPO1 and β-catenin are both required for Wnt4 activation [Manuylov et al., 2008; Liu et al., 2009]; Wnt4 expression is activated by β-catenin stabilization in a positive feed-back regulatory loop [Chang et al., 2008]. In contrast, both Wnt4 expression and Axin2LacZ staining are lost in XX Rspo1–/– mutants [Chassot et al., 2008], hinting that RSPO1 could serve as a common cofactor for the multiple Wnts that are reported to be present in the ovary [Cederroth et al., 2007]. In addition to the shared defects between Rspo1 and Wnt4 mutant animals, further evidence that these 2 genes may cooperate to promote the ovarian pathway came from a study of a human XY patient with male-to-female sex reversal. This patient carried a duplication in the region of chromosome 1 that contains both the WNT4 and RSPO1 loci [Elejalde et al., 1984; Jordan et al., 2001]. In vitro, both RSPO1 and WNT4 are able to activate β-catenin [Binnerts et al., 2007; Wei et al., 2007; Kim et al., 2008]; this activation likely relies on the recently described compound receptor complex that includes LGR receptors. A better understanding of the cooperation between RSPO1 and WNT4 should come from exploring the roles of the LGR4/5/6 family of receptors in the ovary.
The role of β-catenin was also compellingly demonstrated by gain-of-function experiments, where activation of this regulator in the SF1-positive cells resulted in partial XY sex reversal [Maatouk et al., 2008]. The mechanism of ß-catenin-induced sex reversal is not completely understood. It likely involves competition with Sox9 at the transcriptional or post-transcriptional level [Chang et al., 2008; Maatouk et al., 2008; for review, see Tevosian and Manuylov, 2008]. In support of this hypothesis, Sox9 gain of function in the XX sex reversal model also suppresses Axin2LacZ expression [Chassot et al., 2008], and the stabilization of β-catenin in testes leads to a loss of both Sox9 and Amh expression [Chang et al., 2008].
Mice lacking a functional Rspo1 develop ovarian defects similar to Wnt4 mutants, where ovarian development is impaired without a complete sex reversal [Chassot et al., 2008; Tomizuka et al., 2008]. Similarly, while loss of function experiments firmly established that canonical Wnt signaling is a prerequisite step for the gonadal commitment towards an ovarian fate, loss of β-catenin, while detrimental to ovarian development, did not result in the concomitant upregulation of testis-specific genes [Manuylov et al., 2008; reviewed in Tevosian and Manuylov, 2008; Liu et al., 2009, 2010]. These results once again reinforced the notion that ovarian differentiation engages more than one pathway and that all of them would have to be simultaneously disabled to shift the balance towards the male fate (fig. 1).
Given their joint involvement in regulating canonical Wnt signaling, the collaboration between WNT4 and RSPO1 was not all that surprising. In contrast, the Wnt4-dependent genes and the ones that are regulated by FOXL2 appear to control complementary, rather than overlapping, pathways. The hypothesis that ovarian differentiation is autonomously guided by these 2 proteins (or rather pathways) is resting on several pieces of evidence and has been put forward most compellingly by Schlessinger and colleagues [e.g. Ottolenghi et al., 2007b; Schlessinger et al., 2010]. First, consistent with at least partial autonomy, Foxl2 and Wnt4 were each still expressed when the other gene was ablated [Ottolenghi et al., 2007b; Chassot et al., 2008; Manuylov et al., 2008]. Secondly, comparative analysis of gene expression in XX Wnt4–/– and Foxl2–/– gonads by microarray suggested that WNT4 and FOXL2 regulate largely non-overlapping sets of genes. For example, the expression of genes with roles in glucose metabolism and protein synthesis was increased in Foxl2-null ovaries but decreased in Wnt4-null ovaries; on the contrary, genes encoding proteins involved in cell-cell interactions and neuronal-like pathways were downregulated in Foxl2-null ovaries but up-regulated in the absence of Wnt4 [Garcia-Ortiz et al., 2009]. It has also been demonstrated that in goat, gRSPO1 (which is tightly linked to WNT4/β-catenin signaling) and gFOXL2 are localized to spatially separate ovarian domains [Kocer et al., 2008]; this distribution has yet to be tested in other species. Finally, and most importantly, while Foxl2 or Wnt4 alone may not be sufficient to determine ovarian fate, analysis of mice with deficiencies in both Foxl2 and Wnt4 lent support to the notion that the 2 factors may act in a cooperative manner to establish a female sexual identity [Ottolenghi et al., 2007b]. Deletion of both Foxl2 and Wnt4 resulted in testis differentiation in XX mice, including the formation of testis cords, the expression of Sox9 and Amh/Mis, and the differentiation of germ cells into spermatogonia. Still, the sex-reversal phenotype only becomes pronounced near the time of birth and is not fully penetrant, with ovarian somatic cells and oocytes still present. While the ‘two-hit’ mechanism for the sexual determination of the ovary appears quite persuasive, the activity of the Foxl2LacZ reporter gene [Schmidt et al., 2004] is comparable between the Wnt4 null mutant and the double Wnt4–/–; Foxl2–/– knockout [Uhlenhaut et al., 2009]. This observation led the authors to conclude that Wnt4 does not synergize with Foxl2 during embryonic development [Uhlenhaut et al., 2009].
The embryonic development of the Foxl2 mutant ovary proceeds apparently as normal; however, shortly after the time of birth, Foxl2 null gonads begin drifting towards testis differentiation in what was initially described as a secondary partial sex reversal [Ottolenghi et al., 2005, 2007a]. The critical role of Foxl2 in maintaining ovarian identity has been recently confirmed by an elegant study that revealed a novel function of this gene [Uhlenhaut et al., 2009]. The inducible deletion of Foxl2 in adult ovarian follicles leads to the upregulation of Sox9, the transdifferentiation of granulosa cells into Sertoli cells, and the appearance of testis structures and functional testis cell types. Foxl2 deletion also leads to an acute demise of ovarian gene expression with concomitant oocyte loss. To perform its guardian role in maintaining the integrity of the female ‘makeup’, FOXL2 serves as a direct repressor for Sox9 through its gonad-specific TESCO enhancer module. In this repression, FOXL2 is assisted by estrogen receptors. Both FOXL2 and estrogen regulation are required to sustain the granulosa cell phenotype, as granulosa cell transdifferentiation into Sertoli cells has also been observed in the adult ovaries of the estrogen receptor alpha and beta double knockout (ERαβKO) and the aromatase knockout mice [Dupont et al., 2000, 2003; Britt et al., 2004]. While undoubtedly a part of FOXL2 custodial duties, the ability to suppress Sox9 is not likely to be the only sentry point for FOXL2-dependent ovarian fate maintenance. Sox9 is dispensable for testis differentiation once the sex determination mission is accomplished [Chang et al., 2008; Barrionuevo et al., 2009] and other genes (e.g. Sox8 [Chaboissier et al., 2004] or Dmrt1 [Matson et al., 2011], see below) may constitute equally important targets that are in need of FOXL2 repression.
While the inherent lability of the adult ovarian state was arguably predictable [e.g. Ottolenghi et al., 2007a], the recent discovery of extensive reprogramming in the testis upon loss of Dmrt1 was quite unexpected [Matson et al., 2011]. These results suggest that an antagonism between the transcription factors FOXL2 and DMRT1 is critical to uphold the stability of the differentiated gonadal state of the adult. These 2 groundbreaking publications [Uhlenhaut et al., 2009; Matson et al., 2011] expose a long-anticipated plasticity in the gonadal differentiation of both sexes.
Another enduring problem that was valiantly confronted by Uhlenhaut et al.  concerned the oocytes’ role in the postnatal transdifferentiation of granulosa cells into Sertoli cells. In contrast to the continuous FOXL2 expression that is necessary for maintaining female-specific gene expression and ovarian cell fate, the targeted genetic ablation of oocytes proved them to be dispensable for the carrying out of these duties. While germ cell ablation does not induce granulosa cell transdifferentiation, this fact alone does not necessarily prevent germ cells from having a say in somatic cell development, and oogonia or oocytes likely possess some anti-testis properties [Yao et al., 2003].
We still have much to learn about gonadal development, and the recent reports on the remarkable ability of ovaries, and now testes, to transdifferentiate are yet further proof that surprising discoveries are on their way. Upon mentioning transdifferentiation, one is compelled to address ‘the other’ subject now equally in vogue: microRNA. Several groups have reported abnormal postnatal ovarian development upon Dicer ablation in mice using Amhr2-Cre [Hong et al., 2008; Nagaraja et al., 2008; Lei et al., 2010], and we are bound to learn more about specific microRNAs that control ovarian function. However, the extent of microRNA involvement in granulosa cell differentiation during embryogenesis appears limited, as Dicer ablation using the SF1-driven Cre (Sf1Cre) did not produce a notable ovarian phenotype [Huang and Yao, 2010].
The powerful genetic approaches available in mice will undoubtedly keep them as the species of choice for reproductive research aimed at hunting for new genes that have roles in sexual development [e.g. Munger et al., 2009]. Additionally, mice with inducible gonad-specific Cre recombinases should permit the re-examining of the previously known genes that have already been implicated in sexual development, for example, in cases where the null phenotypes show defects in gonad formation, rather than subsequent sexual differentiation. Still, even the most ardent murine aficionado has to keep the perspective that mice cannot tell us everything about ovarian organogenesis in other species, including humans [Jimenez, 2009]. Here too, whole genome sequencing technologies are bound to uncover novel sex determination genes in patients with DSD [Arboleda and Vilain, 2011]. The epigenetic regulation of sexual development remains largely unexplored and will likely be a fruitful field for the future.
I would like to thank Maria Padua and Ramji Bhandari for their thoughtful comments on this manuscript and the NIH for their continuous support (HD042751).
Sergei G. Tevosian
Department of Physiological Sciences, College of Veterinary Medicine
University of Florida, 1333 Central Drive
Gainesville, FL 32601 (USA)
Tel. +1 352 294 4364, E-Mail email@example.com
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher or, in the case of photocopying, direct payment of a specified fee to the Copyright Clearance Center.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.