NR5A2 Regulates Lhb and Fshb Transcription in Gonadotrope-Like Cells In Vitro, but Is Dispensable for Gonadotropin Synthesis and Fertility In Vivo

Successful mammalian reproduction depends on proper synthesis of the pituitary-derived glycoprotein hormones, luteinizing hormone (LH) and follicle-stimulating hormone (FSH). Several transcription factors cooperate to activate cell-specific and hormone-regulated expression of the gonadotropin beta subunits (Lhb and Fshb). Among these, NR5A1 (steroidogenic factor 1; SF1) has been shown to directly bind to the Lhb promoter, mediate basal and gonadotropin-releasing hormone (GnRH)-stimulated Lhb transcription, and possibly directly regulate Fshb expression. Recently, the closely-related NR5A2 was shown to activate the rat Lhb promoter in vitro. Here, we further characterized the role of NR5A2 in regulating gonadotropin synthesis. Ectopically expressed NR5A2 directly activated the murine Lhb promoter in a manner identical to that of NR5A1, whereas neither factor activated the murine Fshb promoter. In LβT2 gonadotrope-like cells, depletion of endogenous NR5A1 or NR5A2 impaired basal and GnRH-stimulated Lhb and Fshb transcription. To analyze the physiological role of NR5A2 in gonadotropes in vivo, we generated mice with a gonadotrope-specific deletion of Nr5a2. In contrast with our in vitro data, these mice had normal pituitary Lhb and Fshb expression and intact fertility. Together, our data establish that NR5A2 can act in a non-redundant manner to regulate Lhb and Fshb transcription in vitro, but is dispensable in vivo.


Introduction
The pituitary-derived gonadotropins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH), are critical regulators of gonadal function and fertility in mammals. LH and FSH are dimeric glycoproteins composed of a common a subunit (aGSU or CGA) and unique b subunits (LHB and FSHB), which confer biological specificity. Lhb and Fshb expression, which is ratelimiting in the production of the mature hormones, is under the control of several endocrine, paracrine, and autocrine factors [1,2]. Most important for Lhb production is gonadotropinreleasing hormone (GnRH). GnRH is released in a pulsatile manner by a small set of neurons within the preoptic area and mediobasal hypothalamus, binds the GnRH receptor (GnRHR) on gonadotrope cells of the anterior pituitary gland, and potently stimulates LH release and synthesis [3,4]. LH in turn regulates steroidogenesis by the testes and ovaries, and is critical for ovulation and luteinization in females [5,6].
Multiple factors control the cell-specific and hormone-induced expression of Lhb and Fshb. GnRH regulation of Lhb is mediated primarily through extracellular regulated kinases 1 and 2 (ERK1/ 2)-dependent induction of early-growth response 1 (EGR1) [7,8]. EGR1 then acts in concert with NR5A1 (also known as steroidogenic factor 1; SF1) and paired-like homeodomain transcription factor (PITX) proteins at conserved cis-elements within the proximal Lhb promoter to activate transcription (reviewed in [2]). How GnRH stimulates expression of Fshb is less well understood and may differ between species [1]. NR5A1's central role in gonadotrope function is perhaps most clearly demonstrated in mice with pituitary-specific deletion of Nr5a1 [9], which display hypogonadotropic hypogonadism, with undetectable basal expression of Lhb, Fshb, and Gnrhr. Studies in cell lines implicate NR5A1 as a direct transcriptional regulator of all three of these genes, as well as Cga [10,11,12,13,14,15]. Nonetheless, Nr5a1 knockout mice retain the ability to produce LH and FSH in response to exogenous GnRH stimulation [9,16]. These data suggest that NR5A1 is dispensable for GnRH-stimulated gonad-otropin production or that another (perhaps related) factor might substitute for its absence. Consistent with the latter possibility, mutation of a conserved ''gonadotrope-specific element'' (GSE or NR5A1 binding site) in the bovine Lhb promoter abolishes its GnRH responsiveness in transgenic mice [17]. Therefore, the available data collectively suggest a more important role for the GSE than for the NR5A1 protein itself in mediating the transcriptional response of the Lhb gene to GnRH.
NR5A2 (also known as liver receptor homolog 1; LRH-1) shares a high degree of sequence homology with NR5A1, binds the same consensus DNA sequence, and regulates many of the same genes [18,19]. Despite their functional overlap, global and cell-specific knockout studies in mice clearly show that the two proteins play distinct roles [20,21]. NR5A2 is expressed in adult murine pituitary gland and in immortalized gonadotrope-like cell lines, and can bind and activate the rat Lhb promoter in vitro [22,23]. Here, we investigated NR5A2's regulation of basal and GnRHstimulated murine Lhb and Fshb transcription in immortalized cells and then ablated the gene specifically in gonadotropes in mice. Whereas NR5A2 is a potent regulator of gonadotropin b subunit promoter activities in vitro, it is dispensable for normal gonadotrope function and fertility in vivo. Figure 1. Characterization of a pituitary-specific Nr5a2 mRNA isoform. A) Schematic representation of the Nr5a2 locus, Nr5a2 mRNA isoforms, and the resulting protein products. Black boxes indicate coding exons; white boxes indicate non-coding sequences. The asterisk (*) after exon 3 denotes the fact that it comes in two forms: the shorter, canonical form (denoted in black) first described in isoforms 1 and 2, and a 59extended form (denoted by the gray extension at the 59 end) expressed in the pituitary (as mapped by 59RACE in this study). Arrows indicate the alternative translation start sites in exons 1 and 3. AF-1, activation function 1; DBD, DNA-binding domain; Ftz, fushi tarazu F1-like box; LBD, ligandbinding domain; AF-2, activation function 2. B) PCR analysis of cDNA prepared from murine liver and pituitary. A common antisense primer in Nr5a2 exon 6 was used in all the reactions. Sense primers were located in exon 2, 3, 4 or 5 as indicated. Amplification of Rpl19 was used as a positive control for cDNA integrity. doi:10.1371/journal.pone.0059058.g001
Cell culture, reporter assays, and western blot LbT2 cells ( [25]; gift from Dr. P. Mellon, University of California, San Diego) and CHO cells (ATCC CCL-61; gift from Dr. P. Morris, Population Council, New York, NY) were cultured as previously described [26,27]. For reporter assays, LbT2 cells were seeded at 3610 5 cells per well in 48-well plates three days before transfection with Lipofectamine 2000. HeLa cells (ATCC CCL-2; gift from Dr J. Tanny, McGill University, Montréal) were cultured in DMEM supplemented with 10% FBS, and plated at 1.8610 4 cells per well in 48-well plate for reporter assays. Cells were transfected the next day using Lipofectamine 2000. Reporter assays were performed as previously described [28]. For western blots, CHO cells in 10-cm dishes were transfected using Lipofectamine following the manufacturer's instructions. Whole cell lysates were prepared and analyzed as described [26].

Plasmids
The murine 2232/+5 Lhb-luc and 21990/+1 Fshb-luc reporters, as well as the EGR1, NR5A1 and PITX1 expression vectors were described previously [24,26,29,30]. The murine 21772/+38 Gnrhr-luc reporter was a gift from Colin Clay (Colorado State University, Fort Collins, CO). The full-length and short isoform (variant #2) NR5A2 expression vectors were produced by PCR amplification from full-length NR5A2 in pCMX [31] and sub-cloned in the EcoRI and XbaI sites of pcDNA3.0. The same strategy was used for generation of FLAGtagged NR5A2 constructs, except that the forward primers replaced the translation initiation codon (ATG) with CGA, and the products were cloned in-frame downstream of a FLAG tag in pcDNA3.0 [30]. Mutant reporters and expression vectors were produced by site-directed mutagenesis following the QuikChange protocol (Stratagene).

rapid amplification of cDNA ends (RACE)
59RACE was performed using the FirstChoice RLM-RACE kit (Ambion, Austin, TX), following the manufacturer's protocol. Briefly, following 59 RACE adapter ligation to decapped total murine pituitary RNA, first-strand cDNA synthesis was performed using an Nr5a2 gene-specific primer in exon 3. Two rounds of nested PCR were performed using forward primers in the 59RACE adapter and reverse gene-specific primers in exon 3 of Nr5a2. PCR products were cloned in pGEM-T Easy (Promega, Madison, WI) and sequenced (GenomeQuébec, Montréal).

FACS sorting of primary gonadotrope cells
For gonadotrope purification, adult (.6 week-old) male and female Nr5a2 fl/fl ;Gnrhr GRIC/+ ;ROSA26 eYFP/+ and Gnrhr GRIC/+ ;RO-SA26 eYFP/+ mice were sacrificed by CO 2 asphyxiation. Dissected pituitaries were collected in M199 media containing 10% FBS, washed three times in HBSS, and minced with a scalpel in a Petri dish. Minced pituitaries were digested in 1.5 mg/mL collagenase (Sigma #C-0130; diluted in Hank's Balanced Salt Solution HBSS with 30 mg/mL BSA, pH 7.4) at 37uC for 2 h with gentle stirring (40 mL/pituitary). The tissue suspension was then washed with 10 mL calcium-free HBSS, centrifuged for 5 min at 12006 g, and resuspended in pancreatin solution (Sigma P3292; 4.5 mg/mL in calcium-free HBSS; 40 mL/pituitary). Pancreatin digestion was performed in a 37uC water bath with manual agitation for 15 min. The resulting cell suspension was washed three times in 10 mL M-199 media supplemented with 10% FBS, with centrifugation steps between each wash as above, and filtered with a 40 micron nylon mesh. The final cell pellet was resuspended in 1 mL M-199 media, and the cells sorted using a FACSAria cell sorter. Both YFPpositive (i.e., gonadotropes) and YFP-negative (i.e., non-gonadotropes) were used in subsequent analyses. . NR5A2 activate the murine Lhb promoter through conserved GSE elements. A) Alignment of the proximal LHB/Lhb promoters from human, mouse, rat and cow. Bases are numbered relative to the transcriptional start site (+1; not shown). The conserved GSE, EGR and PITX response elements are boxed. Nucleotides that differ between the species are shaded. B) and C) HeLa cells were transfected with 225 ng/well of the murine 2232/+5 Lhb-luc reporter or the same reporter carrying a mutation in both GSE elements (GSEmut), along with 50 ng/well of B) NR5A2 (pituitary isoform) or C) NR5A1 expression vectors (black bars) or empty vector (pcDNA3 -white bars). Bars with different symbols differ significantly. Data represent the mean + SEM of five (B) and four (C) independent experiments performed in triplicate. doi:10.1371/journal.pone.0059058.g003 RNA extraction, cDNA synthesis and qPCR Total RNA was extracted from cells (Allprep DNA/RNA, Qiagen) or tissues (TRIzol, Invitrogen), following the manufacturer's instructions. cDNA was prepared as previously described [26]. Quantitative PCR (qPCR) was performed using the Platinum SYBR Green qPCR SuperMix-UDG (Invitrogen) on a Corbett Rotor-Gene 6000 instrument. Samples were assayed in duplicate or triplicate, and analyzed using the 2 2DDCt method [35]. qPCR primers are listed in Table S1.

Hormone assays
For serum collection, mice were killed by CO 2 asphyxiation, and blood obtained by cardiac puncture. The blood was left to clot for 15 minutes at room temperature, and then spun at 3000 rpm for 10 minutes for serum isolation. Serum LH and FSH were

Statistical analysis
Data from the cell culture experiments were analyzed using one-or two-way ANOVA, with Tukey post-hoc test to assess differences between groups. For all the reporter experiments, ''N'' is equal to the number of experiments. In some reporter experiments, data were log-transformed when variances were unequal between groups. Data from the animal experiments were analyzed using independent t-tests. P-values ,0.05 were considered statistically significant.

A short Nr5a2 mRNA isoform is expressed in the murine pituitary gland
Because previous results indicated that NR5A2 from whole pituitary or gonadotrope-like cell lines migrated faster than in vitro translated full-length (liver-derived) NR5A2 in western blots [22], we first mapped the transcription start site of Nr5a2 in murine pituitary by 59 rapid amplification of cDNA ends (59 RACE). Analyses of several independent clones indicated that transcription is initiated in the second intron, 217 base pairs (bp) upstream of the third exon ( Fig. 1A; GenBank acc. # JX648197). The resulting mRNA likely utilizes the previously described start of translation in exon 3 [36], producing an isoform lacking the N-terminal 61 amino acids of the full-length protein, which constitutes most of the AF1 domain (''NR5A2 variant #2'', CCDS acc. # NP_001153241). To confirm the 59 RACE results, murine liver and pituitary cDNAs were analyzed by PCR using a reverse primer in exon 6 and forward primers in exons 2, 3, 4, or 5. Whereas a product was detected with all primer pairs using liver cDNA, no product was obtained from pituitary cDNA with the forward primer in exon 2, confirming that pituitary transcripts lack this exon (Fig. 1B). In subsequent experiments, we used an expression vector encoding the pituitary NR5A2 isoform.

NR5A2 activates the murine Lhb promoter
To determine whether NR5A2 can induce murine Lhb transcription, we examined the effect of ectopic NR5A2 expression on transcriptional activity of the proximal murine Lhb promoter in heterologous HeLa cells. NR5A2 robustly induced the murine -232/+5 Lhb-luc reporter ( Fig. 2A) and did so to a similar extent as NR5A1 (Fig. 2B). NR5A1 cooperatively activates the LHB/Lhb promoter with early-growth response 1 (EGR1) and paired-like homeodomain (PITX) transcription factors [10,24,37,38,39,40]. To assess whether NR5A2 can mediate similar functional interactions, we examined the effect of ectopically expressed NR5A1 or NR5A2 in combination with EGR1 and/or PITX1 on transcriptional activity of the murine Lhb-luc reporter in HeLa cells. All four factors individually activated the Lhb promoter, and EGR1 synergized with PITX1 ( Fig. 2A-B). Furthermore, both NR5A1 and NR5A2: 1) synergized with EGR1, 2) had no significant effect on PITX1-mediated transcription, and 3) did not further amplify the synergism between EGR1 and PITX1 ( Fig. 2A-B). Therefore, NR5A1 and NR5A2 produced indistinguishable functional interactions with EGR1 and PITX1 on the murine Lhb promoter in heterologous cells.
Activation of the LHB/Lhb promoter by NR5A1 requires two conserved response elements (GSEs at 2128/2121 and 266/ 259 relative to the transcription start site in mouse), which neighbor adjacent EGR1 and PITX binding sites in the proximal promoter ( [10,17,24,37,38,39,40] ; Fig. 3A). Because NR5A1 and NR5A2 share identical consensus DNA binding sites, we examined whether the NR5A2 response was also mediated through these two GSEs. To this end, we assessed the effect of ectopic NR5A2 expression on murine 2232/+5 Lhb promoterreporters lacking the distal, proximal, or both GSEs. Mutation of either one or both elements abolished induction of the promoter by NR5A1 or NR5A2 (Fig. 3B-C and Fig. S1).
Two putative GSEs (2341/2333 and 2239/2231) in the murine Fshb promoter were previously shown to regulate basal promoter activity in cooperation with NF-Y binding sites [13]. However, direct actions of NR5A1 on Fshb transcription via these (or other) cis-elements were not demonstrated. Therefore, we examined the ability of NR5A1 or NR5A2 to induce the murine 21990/+1 Fshb-luc reporter in HeLa cells. Unlike the case with the Lhb reporter, neither NR5A1 nor NR5A2 activated Fshb promoter activity (Fig. S2). Co-expression of NR5A1 or NR5A2 with PITX1 also failed to stimulate the Fshb promoter (data not shown).

Endogenous NR5A2 regulates basal and GnRH-induced Lhb and Fshb promoter activities in LbT2 cells
Next, we evaluated the role of endogenous NR5A1 or NR5A2 in basal and GnRH-stimulated transcriptional activity of the murine Lhb and Fshb promoters in homologous LbT2 cells. We cotransfected cells with the murine 2232/+5 Lhb-luc reporter and short interfering RNAs (siRNAs) directed at Nr5a1, Nr5a2 (isoform #2), or with a control siRNA, and stimulated with GnRH. Nr5a1 and Nr5a2 siRNAs significantly decreased basal and GnRHstimulated promoter activity (Fig. 4A-B). The efficiency and sequence specificity of the siRNAs was verified in control experiments ( Fig. S3A and Ref. [24]). In addition, one Nr5a2 siRNA, which displayed poor efficiency at knocking down NR5A2 (siRNA #2), did not affect GnRH-stimulated promoter activity (Fig. S3B-C).
Although ectopically expressed NR5A1 or NR5A2 failed to activate Fshb promoter activity in heterologous HeLa cells (Fig. S2), we examined the effect of depleting endogenous NR5A1 or NR5A2 on the activity of the murine 21990/+1 Fshb-luc reporter in LbT2 cells. Similar to the Lhb promoter, both the Nr5a1 and Nr5a2 siRNAs significantly decreased basal and GnRH-stimulated activation of the 21990/+1 Fshb promoter ( Fig. 4C-D). As observed with the Lhb promoter, Nr5a2 siRNA #2 did not significantly impair GnRH stimulation of the Fshb promoter (Fig. S3D).

Generation of gonadotrope-specific Nr5a2 knockout mice
The in vitro data above show that NR5A2 is expressed in pituitary and functions similarly to NR5A1 with respect to Lhb promoter activity. To test whether NR5A2, like NR5A1, plays an essential role in gonadotropin synthesis and fertility in vivo, we generated mice with a gonadotrope-specific deletion of Nr5a2 by crossing Gnrhr GRIC mice with Nr5a2 fl/fl mice. As loxP sites flank exons 4 and 5 in this Nr5a2 allele, these mice are expected to lack both the full-length and shorter NR5A2 isoforms. Recombination of the Nr5a2 gene was only observed in pituitary gland and in testes (Fig. 5A), as expected from the previously described expression pattern of Cre recombinase in Gnrhr GRIC mice [41]. To assess the efficiency of recombination of Nr5a2 in our model, we bred the ROSA26 eYFP reporter allele [33] into the Nr5a2 fl/ fl ;Gnrhr GRIC/+ background. In the resulting mice, expression of Cre recombinase in gonadotropes results in the simultaneous deletion of the Nr5a2 gene and expression of YFP. We purified gonadotropes (YFP + cells) from Nr5a2 fl/fl ;Gnrhr GRIC/+ ;RO-SA26 eYFP/+ mice by FACS (Fig. S4) and examined the extent of Nr5a2 recombination by PCR. YFP + cells showed the expected PCR product for the recombined allele, indicating the near complete deletion of Nr5a2 in those cells (Fig. 5B). By comparison, cells in the YFP-fraction only showed a band corresponding to the ''floxed'' (non-recombined) Nr5a2 allele. Therefore, Nr5a2 was efficiently and specifically recombined in gonadotropes in our model.
Normal gonadotropin synthesis and fertility in gonadotrope-specific Nr5a2 knockout mice As our in vitro data suggested a role for NR5A2 in the regulation of both Lhb and Fshb transcription, we examined the expression of these genes in the pituitaries of 6 week-old Nr5a2 fl/fl ; Gnrhr GRIC/+ (hereafter Nr5a2KO) mice and Nr5a2 fl/fl (hereafter ''control'') littermates. These analyses revealed no significant difference in the expression of either Lhb or Fshb between genotypes, both in males and females (Fig. 6A-B). Accordingly, serum levels of FSH were normal in Nr5a2KO male and female mice, whereas LH levels were highly variable and often undetectable in mice of both sexes and genotypes ( Fig. 6C and data not shown). Next, we assessed reproductive function in Nr5a2KO mice by monitoring the fertility of males and females after pairing with wild-type C57BL/6 control mice over a period of 6 months. These studies revealed normal fertility in Nr5a2KO mice, as neither males nor females differed from controls in terms of mean litter size, inter-litter interval, latency to first litter, or cumulative number of pups produced over the duration of the mating trial (Table 1). Finally, we examined gonads and accessory sex organs in Nr5a2KO mice (testes and seminal vesicles in males; ovaries and uteri in females). All of the examined tissues were normal in appearance (data not shown) in Nr5a2KO mice and did not differ in weight relative to controls (Fig. S5). Collectively, these results indicate that the activity of the reproductive axis and the production of gonadotropins are intact in gonadotrope-specific Nr5a2 knockout mice.

Nr5a2 is expressed at low levels in murine gonadotropes
Though our 59 RACE results demonstrated Nr5a2 mRNA expression in whole pituitary, the absence of a reproductive phenotype in gonadotrope-specific Nr5a2 knockout mice led us to ask whether the gene is actually expressed in gonadotropes. We first attempted to localize the NR5A2 protein in adult pituitary by immunohistochemistry or immunofluorescence, but were unable to produce consistent results (data not shown). Therefore, we focused on mRNA expression. We developed qPCR assays using Figure 6. Normal gonadotropin synthesis in gonadotrope-specific Nr5a2 knockout mice. cDNA was prepared from total RNA isolated from individual pituitary glands of Nr5a2 fl/fl (control) and Nr5a2 fl/fl ;Gnrhr GRIC/+ (Nr5a2KO) mice, and analyzed for expression of A) Lhb and B) Fshb by quantitative real-time PCR. The amount of Lhb and Fshb transcripts was normalized to the expression of the housekeeping gene Rpl19. For A) and B), n = 6 for control and n = 7 for Nr5a2KO mice, for both males and females. C) Serum FSH levels were measured in 6-week old male (control, n = 5; Nr5a2KO, n = 7) and female (control, n = 4; Nr5a2KO, n = 6) mice. doi:10.1371/journal.pone.0059058.g006 Mice of the indicated genotypes were individually paired with control (C57BL6) mice of the opposite sex for a period of 6 months, and fertility parameters were recorded. Data represent mean 6 SEM. doi:10.1371/journal.pone.0059058.t001 previously validated primers [32] as well as primers within the exons 4 and 5, which are deleted upon recombination in Nr5a2 floxed mice. Nr5a2 is robustly expressed in liver and ovary and we confirmed these observations with both primer sets and total RNA extracted from these tissues in wild-type mice (Fig. 7A). In whole pituitary, Nr5a2 was expressed at only 0.6% the level observed in ovary (Fig. 7A). Using the same cDNA samples, we readily detected Nr5a1 in ovary and pituitary, but not liver (Fig. 7A). To more directly assess expression in gonadotropes, we purified cells from Gnrhr GRIC/+ ;ROSA26 eYFP/+ (control) and Nr5a2 fl/fl ;Gnrhr GRIC/ + ;ROSA26 eYFP/+ (Nr5a2 KO). Whereas Nr5a1 mRNA was enriched in YFP + (i.e., gonadotropes) relative to YFP-(i.e., nongonadotropes) cells, Nr5a2 was uniformly low in both cell populations in both the control and knockout genotypes (Fig. 7B).
In fact, the levels were so low as to preclude a reliable assessment of the extent of mRNA depletion in knockouts. That said, our analysis of DNA from the same purified cells clearly shows how efficiently the floxed allele was recombined (Fig. 5B). Collectively, these data suggest that Nr5a2 is expressed at very low levels in gonadotropes in vivo.

Discussion
Here, we characterized the role of NR5A2 in gonadotropin subunit expression in vitro and in vivo. We identified a novel, pituitary-specific Nr5a2 mRNA isoform in murine pituitary gland. The encoded NR5A2 protein lacks the first 61 N-terminal amino acids of the full-length (canonical) protein, thus truncating most of its ''activator function 1'' (AF-1) domain. In contrast to other nuclear receptors, no specific function has been ascribed to this domain in NR5A2, and all NR5A2 co-regulators characterized to date interact via its C-terminal AF-2 region [18,42]. Accordingly, we observe that the full-length and pituitary NR5A2 isoforms are functionally indistinguishable in their abilities to activate the murine Lhb promoter (data not shown) and do so to an extent and in a manner comparable to NR5A1. Indeed, the NR5A2 response is mediated through the same proximal promoter cis-elements (GSEs) used by NR5A1 [10,24,37,38,39,40]. Furthermore, NR5A2 functionally interacts with other well-characterized transcriptional regulators of Lhb, EGR1 and PITX1 [2,24,40,43], in an identical manner to NR5A1. By knockdown experiments in the LbT2 murine gonadotrope-like cell line, we also show that endogenous NR5A2 regulates both basal and GnRH-stimulated Lhb promoter activation. However, the effect of NR5A1 depletion is more dramatic than that of NR5A2. At least part of the difference might be attributable to the relative roles of NR5A1 and NR5A2 in GnRH receptor expression. Whereas Nr5a1 knockdown significantly impairs Gnrhr promoter-reporter activity, Nr5a2 siRNAs has little to no effect (Fig. S6A). Similarly, whereas Gnrhr mRNA levels are significantly depleted in pituitaries of Nr5a1 knockout mice [9], Gnrhr expression is normal in our Nr5a2KO animals (Fig. S6B). These data suggest that NR5A1 and NR5A2 play similar, though not identical roles in gonadotropelike cells.
The data also show that depletion of either NR5A1 or NR5A2 in LbT2 cells substantially impairs basal and GnRH-stimulated murine Fshb promoter-reporter activity. Exactly how NR5A1 and/ or NR5A2 regulate Fshb expression is presently unclear. Although previous work suggested a requirement for putative NR5A1 binding sites within the proximal promoter for basal Fshb reporter activity [13], a role for the NR5A1 protein itself was not demonstrated in that study. Further, it was previously reported that NR5A1 does not activate the bovine Fshb promoter by itself [44]. In our hands, neither NR5A1 nor NR5A2 induce murine Fshb promoter-reporter activity when ectopically expressed in heterologous reporter assays. However, the dramatic loss of Fshb mRNA and FSH protein in gonadotropes of pituitary-specific Nr5a1 knockout mice [9] certainly suggests a role, either direct or indirect, for NR5A1 in Fshb expression.
Our findings in heterologous and gonadotrope-like cell lines prompted us to investigate the role of NR5A2 in gonadotrope function in vivo. To this end, we generated and analyzed gonadotrope-specific Nr5a2 knockout (Nr5a2KO) mice. We confirm the efficient recombination of the Nr5a2 gene in gonadotropes, in good agreement with the previously demonstrat- Figure 7. Nr5a2 is expressed at low levels in gonadotropes. A) cDNA was prepared from total RNA isolated from the indicated tissues from wild-type mice, and analyzed for the expression of Nr5a1 or Nr5a2. Two different primer sets were used for Nr5a2, with the first using a forward primer in exon 4 and a reverse primer in exon 5 (ex 4-5) and the second with a forward primer in exon 6 and a reverse primer in exon 8 (ex 6-8). B) cDNA was prepared from total RNA isolated from sorted cells from Gnrhr GRIC/+ ;ROSA26 eYFP/+ mice (C-YFP-: YFP-negative cells ; C-YFP +: YFP-positive cells; C = control), Nr5a2 fl/fl ;Gnrhr GRIC/ + ;ROSA26 eYFP/+ mice (KO-YFP-: YFP-negative cells; KO-YFP+: YFP-positive cells; KO = knockout), or wild-type mouse ovary. Expression of Nr5a1 and Nr5a2 (exon 6-8 primer set) was assessed by qPCR, and normalized to the expression of the housekeeping gene Rpl19. In both panels, the results for ovary were normalized to 1 for each primer set and the values for other tissues or isolated cells presented relative to ovary. doi:10.1371/journal.pone.0059058.g007 ed efficiency and specificity of the Gnrhr GRIC allele we used to target Cre expression [34,41,45] Nonetheless, Nr5a2KO mice show normal Lhb and Fshb mRNA expression and circulating gonadotropin levels, and are fertile. Though expressed and functional in LbT2 cells, Nr5a2 mRNA levels are extremely low in actual adult gonadotropes. Thus, the most likely explanation for our results is that, among NR5A family members, NR5A1 (which is maintained at normal levels in our mice), but not NR5A2 is the major regulator of gonadotropin synthesis in vivo.
In summary, we provide in vitro evidence that NR5A2 can mediate transcriptional activation of the murine Lhb and Fshb promoters by GnRH. Moreover, NR5A2 appears to regulate Lhb transcription in a manner analogous to NR5A1. However, unlike the case in Nr5a1-deficient mice, gonadotrope-specific Nr5a2KO animals exhibit normal gonadotropin subunit expression and reproductive function. These observations underscore the importance of in vivo validation of models developed exclusively in immortalized cell lines. Figure S1 Both conserved GSE elements mediate NR5A2 activation of the murine Lhb promoter. HeLa cells were transfected with 225 ng/well of the murine 2232/+5 Lhb-luc reporter or the same reporter carrying a mutation in the proximal (pGSEmut) or distal (dGSEmut) GSE elements along with 50 ng/well of A) NR5A2 (pituitary isoform) or B) NR5A1 expression vectors (black bars) or empty vector (pcDNA3 -white bars). Bars with different symbols differ significantly. Data represent the mean +SEM of five (A) and four (B) independent experiments performed in triplicate. Note that these data are from the same experiments as those shown in Figure 3