Differential expression of WNT4 in testicular and ovarian development in a marsupial
© Yu et al; licensee BioMed Central Ltd. 2006
Received: 10 July 2006
Accepted: 03 October 2006
Published: 03 October 2006
WNT4 is a key regulator of gonadal differentiation in humans and mice, playing a pivotal role in early embryogenesis. Using a marsupial, the tammar wallaby, in which most gonadal differentiation occurs after birth whilst the young is in the pouch, we show by quantitative PCR during early testicular and ovarian development that WNT4 is differentially expressed ingonads.
Before birth, WNT4 mRNA expression was similar in indifferent gonads of both sexes. After birth, in females WNT4 mRNA dramatically increased during ovarian differentiation, reaching a peak by day 9–13 post partum (pp) when the ovarian cortex and medulla are first distinguishable. WNT4 protein was localised in the ovarian cortex and at the medullary boundary. WNT4 mRNA then steadily decreased to day 49, by which time all the female germ cells have entered meiotic arrest. In males, WNT4 mRNA was down-regulated in testes immediately after birth, coincident with the time that seminiferous cords normally form, and rose gradually after day 8. By day 49, when testicular androgen production normally declines, WNT4 protein was restricted to the Leydig cells.
This is the first localisation of WNT4 protein in developing gonads and is consistent with a role for WNT4 in steroidogenesis. Our data provide strong support for the suggestion that WNT4 not only functions as an anti-testis gene during early development, but is also necessary for later ovarian and testicular function.
Sexual development provides an ideal model to study organogenesis since the gonads have the bipotential ability to form an ovary or a testis. Wingless-type MMTV integration site family, member 4 (WNT4) is a member of WNT gene family, and encodes a cysteine-rich secreted protein. WNT4 plays a pivotal role in early embryogenesis, particularly in the formation of the urogenital system [1–4]. After the action of Sry in the XY gonad Wnt4 expression decreases to undetectable levels in the developing testis, but remains at high levels in the ovary . This led to the initial hypothesis that WNT4 acts as an anti-testis gene, blocking Leydig cell differentiation and steroidogenesis in the developing ovary . Lack of Wnt4 results in masculinization of XX mouse embryos  and inhibits the migration of endothelial and steroidogenic cells into the developing ovary , while over-expression of Wnt4 in the developing testis interferes with testicular vascular development and decreases androgen production [5, 6]. Sertoli cell differentiation was also compromised in Wnt4 mutant testes, demonstrating that Wnt4 has specific and distinct roles in both male and female gonadal development .
Wnt4 appears to regulate Dax1 [8, 9], a gene believed to antagonize the function of SRY in the developing gonad. In vitro, Dax1 transcription can be activated by β-catenin, a key signal-transducing protein in the WNT pathway . Besides Dax1, Follistatin (Fst), encoding a TGF-β superfamily binding protein, may also be a downstream component of Wnt4 signalling that regulates vascular boundaries and maintains germ cell survival in the ovary . Furthermore, Wnt4 and fibroblast growth factor 9 (FGF9) act as antagonistic signals to regulate differentiation of the ovary and testis . To date most of our knowledge about the role of Wnt4 in the mammalian gonad has been based on studies only in the mice. In order to determine the role of WNT4 in formation of the mammalian gonad we characterised its expression in a distantly related mammal.
Marsupials give birth after a relatively short gestation to small altricial young that complete their development during a long lactation period attached to a teat, usually in a pouch. The tammar gonadal ridge develops about 6 days before birth, but the gonads remain undifferentiated until after birth [12–14]. Testicular differentiation begins with the formation of seminiferous cords by day 2 post partum. The ovaries, as in all mammals, differentiate after the testis at about day 8 post partum, almost 14 days after the initial development of the gonadal ridge. In contrast to the tammar, the development of the mouse gonad is extremely rapid and there is only 1 day between the formation of the gonadal ridge and the onset of cord formation in males.
Marsupials have the classical mammalian XY sex determining mechanism  with a homologue of SRY on the Y chromosome . However, the formation of some secondary sexual characteristics, including the scrotum and mammary glands, are under primary genetic control by genes on the X chromosome, and are not dependant on hormones from the testis [14, 17, 18]. Several key genes in the sex determination and differentiation cascade, SRY , SOX3 , SOX9 , SF-1 , DAX1 , DMRT1 [24, 25], ATRX/Y [26, 27], AMH/MIS , have now been cloned and characterized. The endocrine control of male sexual differentiation in the tammar has also been defined [29–35]. Taken together, these data form a primary framework for understanding the evolution of the male sex-determining cascade in marsupials. However, nothing is yet known of the female gonadogenesis pathway in marsupials. This study has therefore characterized WNT4 during early development to gain insight into the onset of ovarian differentiation in a marsupial, and also to determine its expression during the extended period of testicular differentiation.
Cloning and characterization of the tammar WNT4Gene
Sequence analysis confirmed that PCR products were derived from the WNT4 gene (data not shown). The longest sequence encodes a predicted protein of 351 amino acids.
WNT4 mRNA distribution
Real-time quantitative PCR
Protein localization in tammar gonads
We report the first molecular characterization and expression pattern of WNT4 in a non-eutherian mammal, the tammar wallaby. This is also the first localization of WNT4 protein in the gonad of any mammal. The greatly extended developmental time of marsupial gonads enabled us to complete the first detailed analysis of the changes in WNT4 expression throughout the whole of this critical developmental period. Since the mouse testis undergoes rapid development, the period of WNT4 down-regulation that we have observed in the tammar testis occurs very rapidly in the mouse and so may have been missed. In the female, WNT4 is upregulated during the time of ovarian differentiation, but is down-regulated by the time the XX germ cells have all entered meiosis. In the male, it is down-regulated by the day of birth when testicular differentiation is occurring, but gradually increases by the time XY germ cells have all entered mitotic arrest. The conserved but differing expression patterns of WNT4 in the wallaby ovary and testis supports the idea that it has a critical role in gonadal development in both sexes.
The structure and role of WNT gene family is highly conserved in vertebrates [36, 37], and even in the sea anemone, a species representing the basal group within cnidarians . However, the full-length WNT4 gene sequence has only been previously characterized in three mammals, and four non-mammalian vertebrates (Fig. 1). The tammar WNT4 gene consists of five exons, exons 2 – 4, the most highly conserved. The tammar WNT4 gene is present as a single copy in the genome of both males and females, indicating it is autosomal, as in other mammals (human: Chr 1 [8, 39, 40], mouse: Chr 4 and rat: Chr 5). WNT4 participates in multiple developmental events during embryogenesis, is broadly expressed in many adult tissues in mice and humans and has also been implicated in adult tissue homeostasis [1–3, 7, 41, 42]. Semi-quantitative RT-PCR expression analyses in adult tammar tissues showed a similar pattern to that of human WNT4 consistent with a conserved and wide role for WNT4 in tissue homeostasis.
WNT4 also appears to be important for the normal pattern formation and development of both the male and female gonad . In our study, using quantitative RT-PCR and immunohistochemistry, WNT4 was expressed at equal levels in the indifferent fetal and neonatal male and female gonads. At this time, protein in the ovary was localized to the somatic cells. Subsequently, WNT4 mRNA expression increased significantly to reach a peak at day 9–13, the time that ovarian cortex and medulla can be distinguished. After ovarian differentiation at day 12–13 postpartum, WNT4 expression remained localized in cortex and at the boundary of the cortex and medulla, but by day 45 pp, there was stronger expression in the medulla. The decreased WNT4 expression in the ovary to a level similar to that in testis, coincides with the time female germ cells enter meiosis .
In the testis, WNT4 gene expression was significantly down-regulated immediately after birth during the initial period of testicular differentiation, coinciding with the formation of seminiferous cords . After cord formation, WNT4 levels increased slowly after day 8 postpartum and became specific to Leydig cells. By day 49, when secretion of testicular testosterone decreases (Fig. 5b) , Leydig cells stained strongly for WNT4. We suggest that once WNT4 reaches a critical threshold level, androgen production diminishes. The low level of immunostaining in the adult testis and ovary is consistent with their increase in steroidogenesis after puberty. This pattern of expression is therefore consistent with the hypothesis that WNT4 blocks initial testis differentiation, because the mRNA concentration is dramatically reduced and the WNT4 protein is localized to the tunica during this period of testicular development.
The two hypotheses for WNT4 action as an anti-testis gene  and as an important factor in testis development  are not mutually exclusive. Our data show that WNT4 is down-regulated for a brief period of time when the testis cords are first formed and the cell types of the testis determined, but then becomes up-regulated after day 10 post partum to control later testicular development. In the ovary, WNT4 remains strongly expressed in the gonad consistent with its role in inhibiting early testicular development and promoting later ovarian differentiation. It may also be important for the maintenance of germ cells in both females and males throughout development. Our data support the conclusion that WNT4 functions not only as an anti-testis gene during early mammalian development, but is also necessary for later ovarian and testicular function.
Tammar wallabies Macropus eugenii of Kangaroo Island (South Australia) origin were maintained in open grassy yards in our breeding colony. Fetuses of each sex were collected at various stages of gestation as previously described [44, 45]. During the breeding season adult females were checked daily for births (designated day 0 pp). In cases in which the day of birth was uncertain, the age of pouch young was estimated using head length from published growth curves . The sex of pouch young was determined by the presence or absence of scrotal or mammary primordia . All sampling techniques and collection of tissues were approved by The University of Melbourne Animal Experimentation & Ethics Committees. All experimental procedures conformed to Australian National Health and Medical Research Council (1990) guidelines and were approved by Institutional Animal Experimentation Ethics Committees.
Ages and numbers of samples of ovaries and testes analysed by real-time PCR
d24(1), d25(4), D0(1)
d25(3), d26(1), D0(1)
D1(1), D1.5(1), D2(1), D2.5(1),
D1.5(1), D2.5(2), D3(1)
D4(1), D6(2), D8(1),
D5(1), D7(2), D8(1),
D9(1), D10(1), D11(1), D12(1), D13(1),
D9(1), D10(1), D12(1), D13(2),
D14(1), D15(1), D15.5(1), D17.5(2), D18(1),
D14(1), D15(1), D16(1), D17.5(1), D18(1), D19(1)
D20(1), D20.5(1), D21(1), D24(2)
D20(1), D20.5(1), D21(1) D22(1), D24(1)
D41.5(1), D42(2), D44(1), D49(1)
D41(2), D44(1), D45(1), D46(1), D47(2), D47.5(1)
Cloning of tammar WNT4 and determining gene structure
Primers designed for the analysis of WNT4 expression by PCR
ATTCTAGAGGCCGAGGCGGCCGACATG-d(T)30N-1N (N = A, G, C, or T; N-1 = A, G, or C)
5' PCR Primer
RT-PCR & qPCR
RT-PCR & Qpcr
Cross species cloning
Cross species cloning
SMART cDNAs were reverse transcribed from total RNAs from fetuses of wallaby, using the SMART cDNA library construction kit (Clontech, Mountain View, California, USA). 5' RACE was performed using Primer 5' PCR Primer and R1. Owing to an incomplete coding sequence at the 5' end, we designed a new primer R2 according to the first sequence results, and repeated 5' RACE. 3' RACE was performed using primer F1 and CDS III, nested PCR was performed using primer F2 and CDS III. PCR cycling conditions were: 35 cycles, with 30s, 94°C; 40s, 64°C or 56°C, 120s, 72°C, in a 20 μl reaction mix containing 10 mM Tris-HCl, pH 8.3, 1.5 mM MgCl2, 50 mM KCl, 200 μM dNTP, 0.2 μM each primer, and 1U Taq DNA polymerase (Promega, Wisconsin, USA).
In order to determine the tammar WNT4 gene structure, a Macropus eugenii BAC library was screened using WNT4 3RACE probe obtained as outlined above. Primers within and spanning intron exon boundaries were designed based on the gene structure of human, mouse and the opossum (deduced from the opossum genome sequence). PCR confirmed the presence of all 4 introns at identical positions to other mammals. We sequenced intron 3 and intron 4 using the BAC plasmid DNA as a template, however, intron 1 and intron 2 were too large to amplify by standard PCR (data not shown).
Alignment and phylogenetic analysis
WNT4 protein sequences, from tammar (GenBank accession number AY940685), human (NP_110388), mouse (NP_033549), Rat (NP_445854), chicken (NP_990114), frog (P49338), zebrafish (AAA96004), Amphioxus (AAC80431), fruit fly (NP_476810) and C. elegans (NP_493668), was aligned by CLUSTALX 1.83 , and edited with GeneDoc). The phylogenetic tree was constructed with PHYLIP 3.63 program (University of Washington), and viewed with TREE-view 1.6.6.
Southern blotting hybridization
Genomic DNA was extracted from the liver of the male and female tammar wallabies according to the standard protocol of Sambrook et al. , digested with EcoRI and SalI/XbaI, electrophoresed in 0.8% agarose gel, and transferred onto a nitrocellulose filter. Hybridization was performed in ULTRAhyb solution (Ambion Inc., Austin, Texas, USA) with [α-32P]dCTP-labeled fragment from primer F2 and CDS III PCR, and autoradiographed.
Total RNA was isolated from tissues using the RNeasy kit (Qiagen Inc, Valencia, California, USA) or GeneElute kit (Sigma, Castle Hill, NSW, Australia), and the quality and quantity of total RNA were verified by two methods, gel electrophoresis and optical density readings with SmartSpec™ 3000 (BioRad Laboratories Inc., Waltham, Massachusetts, USA). 2 μg of total RNA was DNase-treated with DNA-free (Ambion Inc., Austin, Texas, USA). 1 μg of total RNA was reverse transcribed using SuperScript III (Invitrogen, California, USA).
Primers R1 and F2, spanning the second intron and third intron, were designed from the tammar wallaby WNT4 gene structure. PCR was performed in a 50 μl reaction containing 10 mM Tris-HCl, pH 8.3, 1.5 mM MgCl2, 50 mM KCl, 200 μM dNTP, 0.2 μM each primer, 1U Taq DNA polymerase (Promega) and first-strand cDNA products. Amplification conditions were: 94°C, 30s; 60°C (18S) or 56°C (WNT4), 40s; 72°C, 60s for 26 cycles (18S) or 40 cycles (WNT4).
Real-time quantitative PCR
To obtain further insight into roles of WNT4 in sex determination and differentiation, we investigated the WNT4 expression profile at different stages of gonadal development by quantitative RT-PCR. Gonads (free of mesonephros) were divided into six groups, each group consisting of 4–8 samples at each stage. Tammar forward primer qF and reverse primer qR were used for real-time PCR and produced a 102 bp fragment. 18S primers produce a 100 bp fragment as internal reference in the quantitative PCR. Primer pair annealing temperature was optimized for real-time PCR on a temperature gradient program. Primer specificity was confirmed by gel electrophoresis and melt curve analysis. To determine the detection range, linearity and real-time PCR amplification efficiency [E = 10[-1/slope]] of each primer pair, real-time PCR amplifications were run in triplicate on a 10-fold serial dilution of ovary cDNA and standard curves calculated.
cDNA templates from all stages of gonadal development were prepared as above. Real-time PCR was performed on the DNA Engube Opticon 2 by MJ Research Incorporated (BioRad Laboratories Inc., Waltham, Massachusetts, USA). Each sample was amplified in triplicate in a 20 μl reaction volume using 4 μl cDNA (dilution 10 times before using), 10 μl 2X MasterAmp qPCR SYBR Green Fluorescein Mix (F-400, DyNAmo™ SYRB® Green qPCR kit, Finnzymes Oy, Espoo, Finland), 3 μM of the appropriate forward and reverse primers, and then 3 μl H2O to 20 μl final volume. The mixture was incubated at 55°C for 15 minutes, and then at 95°C for 10 minutes to activate the Taq polymerase. This was followed by 40 cycles of denaturation at 95°C for 30 seconds, annealed at 53°C for 20 seconds, extended at 72°C for 35 seconds, and incubated at 76°C for 1 second to read the plate. Finally, a melt curve analysis was constructed from 40 to 95°C.
The initial amplification of PCR product can be dynamically expressed as X n = X0*(1+E) n , where X n is the number of amplified molecules at cycle n, X0 the initial number of template molecules, E the amplification efficiency, and n the number of cycles. In fluorescence dye real-time PCR, X n is proportional to the reporter fluorescence R, so the above equation can be written as R n = R0*(1+E) n , where R n is the reporter fluorescence at cycle n, and R0 the initial reporter fluorescence. Therefore, the relative expression of each sample can be calculated by the following formula: ratio = (1+ERef)CtRef/(1+ETarget)CtTarget. Values can be assessed to create a graph with the smallest value set as "1" according to the above formula. Comparison of the relative WNT4 expression between males and females at each stage and between stages was achieved using analysis of variance with specified contrasts for individual comparisons (Systat 11, Systat software Inc, Point Richmond, California, USA).
Developing testis and ovaries (D30-50pp) and two negative adult heart and BSA were collected. Tissues were homogenised in lysis buffer, and extracted total protein. 10 μg of each protein was boiled in sample buffer, electrophoresed on 12% SDS-PAGE and blotted onto Hybond NC membranes (Millipore Corporate, Massachusetts, USA). Goat anti-hWNT4 polyclonal antibody (Abcam, ab15699, Sapphire Bioscience Pty Ltd, Australia) was used as a primary antibody which was diluted 1:750 in 1% BSA/TBS-T. As a secondary antibody, the peroxidase-conjugated anti-goat immunoglobulin was diluted 1:750 in 1% BSA/TBS-T. Signals were visualized by ECL plus™ detection system (Amersham Biosciences UK Limited, Buckinghamshire, UK).
Tissue sections (8 μm) were treated with 5% hydrogen peroxide in distilled H2O for 10 min to quench endogenous peroxidase activity. Antigen retrieval was achieved by placing slides in boiling sodium citrate buffer (10 mM Sodium Citrate, 0.05% Tween-20, pH 6.0) for 20 min. The primary antibody goat anti-WNT4 polyclonal antibody (Abcam, ab15699) was applied to sections at a 1:200 dilution at 4°C overnight. Signal was amplified using the ABC/HRP kit (DAKO, New South Wales, Australia), visualized with DAB (DAKO), and counterstained with haematoxylin.
α-thalassemia and mental retardation associated with the X/Y chromosome
bovine serum albumin
dosage-sensitive sex reversal, adrenal hypoplasia congenita critical region on the X chromosome, gene 1
Doublesex and mab-3 related transcription factor 1
fibroblast growth factor
steroidogenic factor 1
SRY-like HMG box
sex-determining region of the Y
Transforming Growth Factor
wingless related MMTV integration site.
We thank Dr. Shuliang Cui for helpful suggestions when cloning tammar WNT4 cDNA. We also thank all members of the wallaby research group and in particular Dr. Danielle Hickford for her help with immunohistochemistry and Eleanor Ager for assistance with the real-time PCR. This work was supported by Australian National Health and Medical Research Council grant #251551 to MBR, AJP, GS and Richard Behringer.
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