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Coexistence of Genotypic and Temperature-Dependent Sex Determination in Pejerrey Odontesthes bonariensis

  • Yoji Yamamoto ,

    Contributed equally to this work with: Yoji Yamamoto, Yan Zhang

    Affiliation Graduate School of Marine Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan

  • Yan Zhang ,

    Contributed equally to this work with: Yoji Yamamoto, Yan Zhang

    Affiliations Graduate School of Marine Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan, College of Fisheries and Life Science, Shanghai Ocean University, Shanghai, China

  • Munti Sarida,

    Affiliation Graduate School of Marine Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan

  • Ricardo S. Hattori ,

    shuheibio@yahoo.co.jp

    Affiliation Graduate School of Marine Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan

  • Carlos A. Strüssmann

    Affiliation Graduate School of Marine Science and Technology, Tokyo University of Marine Science and Technology, Tokyo, Japan

Coexistence of Genotypic and Temperature-Dependent Sex Determination in Pejerrey Odontesthes bonariensis

  • Yoji Yamamoto, 
  • Yan Zhang, 
  • Munti Sarida, 
  • Ricardo S. Hattori, 
  • Carlos A. Strüssmann
PLOS
x

Abstract

In this study, we examined whether a homolog of the master sex-determining gene amhy of Odontesthes hatcheri is present and plays any role in testis determination of pejerrey O. bonariensis, a species otherwise known for its strong temperature-dependent sex determination (TSD). Screening of wild and laboratory-reared pejerrey for amhy revealed a high, although not complete linkage with phenotypic sex. The sex ratio in an amhy+/−/amhy−/− full sibling progeny reared during the thermolabile period of sex determination at an intermediate temperature of 25°C was 68.7% male:31.3% female; all amhy+/− fish developed as males whereas about 2/3 and 1/3 of the amhy−/− were female and male, respectively. Expression analyses revealed that amhy transcription began during embryo stage and decreased by the end of sex determination period. The autosomal amha was present in all individuals regardless of amhy genotype; its expression increased significantly from the end of the same period in the gonads of all amhy+/− but only in part of the amhy/− animals. After histological gonadal differentiation, all gonads of amhy−/− animals with amha ISH signals were testes and those without it were ovaries. These results suggest that amhy is important for testicular differentiation in pejerrey, at least at intermediate temperatures. Thus, we hypothesize that amhy+/− animals differentiate as males by expression of either amhy alone or amhy and amha together whereas the amhy−/− probably rely solely on amha expression. These findings represent the first clear genomic evidence that genotypic and environmental sex determinants can coexist in species with marked TSD such as the pejerrey. The finding of amhy will make possible to monitor wild pejerrey populations for mismatches between genotypic and phenotypic sex and may prove instrumental for field studies addressing the effects of endocrine disruptors or abnormal temperatures on reproduction and the ecological relevance of TSD for this species.

Introduction

The pejerrey Odontesthes bonariensis is an excellent model for the study of temperature-dependent sex determination (TSD) in teleosts. In this species, sex ratios reach 100% female or 100% male at environmentally relevant temperatures of 17°C (female producing temperature, FPT) and 29°C (male producing temperature, MPT), respectively. The critical time of sex determination has been estimated between 1 and 5 weeks after hatching (wah) depending on the water temperature [1]. The end of this period coincides with the beginning of the histological differentiation of the gonads, which occurs first in ovaries and then in testes [2]. In addition, significant information on the molecular and biochemical processes underlying its TSD is available. For example, differential expression of fshb (follicle stimulating hormone beta) and lhb (luteinizing hormone beta) in the pituitary and of lhr (luteinizing hormone receptor), cyp19a1a, dmrt1, and amh in the gonads were found to be involved in the sex differentiation process [3][5]. Other studies have shown a connection between environmental temperature and sex determination that is mediated by the glucocorticoid stress-related hormone cortisol, in particular during masculinization [6], [7]. Thus, significant advances have been achieved concerning the mechanism of TSD in pejerrey but, as discussed next, the picture is far from complete.

While the reproducible sex ratios consistently obtained at the FPT (all-female) and MPT (all-male) suggest that genotypic sex determinants in O. bonariensis are virtually inexistent, this is not a foregone conclusion. For example, at intermediate, mixed sex-producing temperatures (MixPT; around 24–26°C), large variability in sex ratios (e.g. 20–80%) is observed between progenies from different parents at a given temperature. Such variability could be related to subtle, hitherto unknown environmental effects besides temperature or it could be an indication that parents carry some form of genotypic gender determinant that affects sex determination at sexually neutral temperatures [1]. The latter scenario has become more plausible after a recent study on the sex-determining mechanism of the congeneric species O. hatcheri (Patagonian pejerrey), which possesses a typically balanced (1∶1) sex ratio at intermediate temperatures, revealed a male-specific duplication of the amh gene (called amhy, for Y-linked anti-Müllerian hormone) that triggers testicular development [8]. Because the two species are closely related and share a high genetic identity [9], it is conceivable that amhy could exist in O. bonariensis and be behind the variable sex ratios observed at the MixPT, as it would be the case for example, if any of the parents is a (thermally) sex-reversed animal. It is noteworthy that environment and genotype interactions have been implied before in sex determination of other species with TSD [10][15] but a clear genotypic factor has never been identified.

In this context, this study was designed to probe the presence of amhy in the pejerrey genome and whether it has a role in gonadal sex determination of this species. We successfully cloned an amhy homolog in laboratory-reared pejerrey, genotyped broodstock and wild fish based on amhy, and carried out progeny tests to confirm its sex linkage and Mendelian inheritance. In addition, we examined the ontogeny of amhy expression in relation to that of the autosomal form amha and to time of histological gonadal sex differentiation. The results clearly show that amhy is functionally implicated in testicular differentiation in pejerrey at intermediate, temperatures, and prove the coexistence of environmental and genotypic sex determination in this species.

Materials and Methods

Ethical statement

This study was carried out in accordance with the Guide for the Care and Use of Laboratory Animals from Tokyo University of Marine Science and Technology (TUMSAT). Experiments with fish at TUMSAT do not require any special authorization as long as they adhere to the institutional guidelines, which is the case of this study. Laboratory fish were procured from the Aquatic Animal Rearing Facilities of TUMSAT, which is licensed to keep broodstock and propagate fish, and were sacrificed by anesthetic overdose in order to minimize animal suffering prior to any sampling. All samples of wild fish used in this study were a kind donation from Dr. Seiichi Kasuga, National Institute for Environmental Studies (NIES), Ibaraki, Japan and were already dead when provided to us. These samples were taken in 2001 during routine fisheries resource assessments conducted by the NIES and have been kept frozen until use. Pejerrey is not an endangered species and its collection is not subject to permit requirement.

Cloning and sequencing of pejerrey amhy

To obtain the complete cDNA sequence of the amhy gene in O. bonariensis, total mRNA extracted from the gonad of a laboratory-reared, amhy-positive (amhy+) was used. Extraction of mRNA and synthesis of cDNA were performed according to previous studies [8]. 5′ and 3′ UTR fragments were amplified by the primers listed in Table S1 using GeneRacer (Invitrogen, Carlsbad, CA) and Smart RACE cDNA amplification (Clontech, Mountain View, CA) kits, following manufacturer's instructions. Genomic DNA was extracted following the protocol described by Aljanabi and Martinez [16] and used for intron sequencing. PCR was performed using primers designed on the basis of the O. hatcheri amhy (Table S1; NCBI accession code HM153803). All amplifications were done according to the following conditions: 3 min at 94°C, 30 cycles of 30 sec at 94°C, 45 sec at 60°C and 2.5 min at 72°C, then followed by a final elongation for 5 min at 72°C. PCR products were electrophoresed in 1% agarose gel, purified, and sequenced in an ABI PRISM 3100 capillary sequencer (Life Technologies, Carlsbad, CA) using the BigDye Terminator method. Sequences were analyzed with GENETYX version 11.0 (GENETYX, Tokyo, Japan).

Phylogenetic analysis

The predicted amino acid sequences of pejerrey Amhy and Amha (GeneBank accession numbers KC847082 and AY763406, respectively) were compared to the Amh sequences of other teleosts available at GenBank using the software GENETYX version 11.0. The following sequences were compared: Patagonian pejerrey Amhy and Amha (Odontesthes hatcheri, DQ441594 and HM153803, respectively), Atlantic salmon Amh (Salmo salar, AY722411), zebrafish Amh (Danio rerio, AY721604), Japanese flounder Amh (Paralichthys olivaceus, AB166791), blue tilapia Amh (Oreochromis aureus, DQ257618) and Japanese medaka Amh (Oryzias latipes, AB214971). The phylogenetic tree was constructed by the Neighbor-Joining method [17] using MEGA software (vers. 5.2.2) [18] with 10000 replicates.

amhy genotyping of wild fish and laboratory broodstock

A random sample of 90 pejerrey juveniles collected by seine net in the Lake Kasumigaura (Ibaraki, Japan) on September 2001 and 24 laboratory-reared broodstock fish from the Aquatic Animal Rearing Facilities, Tokyo University of Marine Science and Technology (Shinagawa Campus, Tokyo, Japan), were screened for the presence of amhy using primers designed on the basis of the 5′ flanking region of O. hatcheri amhy (Table S1; NCBI accession code HM153804). The autosomal amh homolog of O. bonariensis (amha; NCBI accession code AY763406) was analyzed using the primers indicated in Table S1 as a positive control. Animals carrying the amhy gene (amhy-positives) were represented by amhy+ when the exact genotype could not be determined and by amhy+/+ or amhy+/− when they were confirmed as homozygous or heterozygous, respectively. Those without amhy (amhy-negative) were represented by amhy−/−. Genomic DNA extraction and amplification followed the protocols described in the previous section. Gonadal sex of each individual was asserted by dissection and visual inspection of the gonads for wild fish, after sacrificing them through procedures described above, or manual stripping of gametes/gonadal cannulation for laboratory broodstock.

After amhy genotyping, laboratory-reared broodstock were used in single-pair crosses between one amhy−/− female and nine amhy+ males were produced by artificial fertilization for testing Mendelian inheritance and whether the males were homozygous (amhy+/+) or heterozygous (amhy+/−). We also performed a progeny test with one amhy+ female and an amhy−/− male. Incubation until hatching was performed as described below. Randomly-chosen hatchlings (n = 24–98) from each cross were analyzed following the same procedures used for wild fish and broodstock genotyping.

Rearing procedures and sampling for mRNA expression analysis

One of the pairs that yielded a balanced sex ratio in the progeny test (amhy−/− female, F1, amhy+/− male, M9; Table S2) was selected and allowed to breed naturally in a 650-liter recirculated-water rearing tank under controlled temperature (20°C), photoperiod (14L/10D), and salinity (0.2–0.5% NaCl in dechlorinated tap water). Fertilized eggs were collected, cleaned of chorionic filaments, and transferred to incubators with flowing brackish water (salinity of 0.2–0.5%) at 19°C. After hatching (about 9 days after fertilization), approximately 800 to 1000 newly-hatched larvae were stocked in each of two 60-liter tanks and reared at 25°C (MixPT) [1], [2] for up to 14 weeks. Fish were fed live Artemia nauplii from the first day to satiation three to four times daily and gradually weaned into powdered fish food (TetraMin flakes, Melle, Germany) from the third week. Fish were sampled daily (0 to 8 days after fertilization, or daf; n = 10) and weekly (0 to 10 wah; n = 20), respectively, for gene expression and histological analyses (see below for details). Larvae and juveniles were fin-clipped for genomic DNA extraction and amhy genotyping according to the methods described in the previous section. The remaining fish (n = 67) were collected at the end of the experiment (14 wah) for histological determination of sex ratios.

Histological analysis of gonadal sex differentiation and sex ratios

For the histological analysis of gonadal sex, trunks were fixed overnight in Bouin's fixative solution, dehydrated in ascending ethanol series, cleared in xylene, and embedded in Paraplast Plus (McCormick Scientific, St. Louis, MO). Cross-sections were cut serially at a thickness of 5 µm, stained with Hematoxylin-Eosin, and analyzed following previously reported histological criteria [2], [19].

Tissue distribution and temporal expression analysis of amhy, amha, and cyp19a1a transcripts

The tissue distribution of amhy and amha transcripts was analyzed using total RNA extracted from testis, brain, gill, heart, trunk kidney, spleen, liver, anterior and posterior intestine, and muscle of an amhy+/− 20 week old juvenile. For the temporal expression analysis, whole embryos and trunks of larvae were stored in RNAlater (Sigma-Aldrich, St. Louis, MO) at −80°C until use. Trizol Reagent (Life Technologies) was used for total RNA extraction. Genomic DNA extracted from the remaining interphase was used for genotyping embryos. All procedures followed the reagent manufacturer's protocol. Synthesis of cDNA and transcription analyses of amhy, amha, and β-actin in whole embryos and juvenile tissues were performed by RT-PCR according to a previous study [8]. In larvae, the same genes were analyzed by qRT-PCR using the specific sets of primers and probes shown in Table S1. The suitability of β-actin as an endogenous control was confirmed by qRT-PCR in the same samples (Fig. S1, see also references [3][7]). The specificity of the primers was confirmed by using plasmids containing amhy or amha ORFs as controls and also by direct sequencing of PCR products. The transcript levels of the ovarian differentiation marker cyp19a1a were analyzed at 4 and 6 wah following methods reported in our previous studies ([4][6]; see also Table S1).

Localization of amhy/amha mRNAs by ISH

Samples for in situ hybridization (ISH) in pre- and post-differentiation gonads were collected at 4 and 10 wah, fixed and processed for preparation of histological sections as described above. Body trunk sections were hybridized in the automated tissue processer Hybrimaster HS-500 (Aloka, Tokyo, Japan) using an amh probe that recognizes both amhy and amha, synthesized according to a previous study [5]. Final detection was performed manually with NBT/BCIP according to the manufacturer's (Roche Diagnostics, Basel, Schweiz) protocols.

Results

Cloning and sequence analysis of amhy gene

An amhy homolog was cloned from a laboratory-reared pejerrey and revealed the amhy-characteristic 0.5 kb fragment within the third intron (Fig. 1A). The deduced Amhy protein, including the characteristic TGF-β domain (amino acids 421–514) with seven canonical cysteine residues, comprised 514 amino acids. Phylogenetic analysis based on the amino acid sequence of the open reading frame showed that O. bonariensis Amhy shared the same clade with O. hatcheri Amhy whereas the Amha in both species were placed together in another clade (Fig. 1B). Among the outgroup species, the medaka Amh showed to have the shortest genetic distance to the Odontesthes species Amhs, displaying similar distances to both Amhy and Amha clades.

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Figure 1. amhy gene structure, phylogenetic relationship, and broodstock genotyping.

A: Structure of the amhy gene in O. bonariensis, size of exons, UTRs, and TGF-beta domain, and the respective identity values in relation to O. bonariensis amha. The third intron contains a 0.5 kb insertion in relation to amha. B: Phylogenetic tree (Neighbor-Joining method) for the amino acid sequences of O. bonariensis and O. hatcheri Amhy and Amha and the Amh of other teleosts. Numbers indicate bootstrap values based on 10000 replicates. C: amhy-based sex genotyping in O. bonariensis broodstock using primers that amplify part of the 5′ flanking region and part of the amhy gene (1896 bp); amha gene was used as positive control (2441 bp). The dotted-boxes indicate parents used in the rearing experiment and asterisks indicate disagreement between the amhy-based genotype and phenotypic sex. NC: negative control.

https://doi.org/10.1371/journal.pone.0102574.g001

Genotyping of wild fish, broodstock, and progeny from specific crosses

The analysis of juveniles from Lake Kasumigaura revealed 38 amhy+ and 52 amhy−/− out of 90 individuals whereas that of our O. bonariensis broodstock revealed 14 amhy+ and 10 amhy−/− out of 24 individuals (Table 1; Fig. 1C). In both cases, there was a high but not complete concordance between genotypic and phenotypic sex. The progeny of all 9 amhy+ males crossed pairwise with the same amhy−/− female showed sex ratios statistically undistinguishable from 1∶1 (Fisher's exact test), indicating that all males were heterozygous (amhy+/−) for the amhy gene (Table S2). No amhy+/+ male was found among the tested fish. Likewise, the cross of an amhy+ female with an amhy−/− male confirmed that the former was heterozygous for amhy (Table S2). As expected, amha was detected in all fish regardless of phenotypic sex or amhy genotype (Fig. 1C).

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Table 1. Relationship between phenotypic (gonadal) sex and amhy genotype in wild pejerrey and laboratory-reared broodstock.

https://doi.org/10.1371/journal.pone.0102574.t001

Tissue distribution and temporal expression analysis of amhy, amha, and cyp19a1a

Transcripts of amhy were found in the testis and in the brain whereas amha was expressed only in the testis of juveniles (Fig. 2A). Transcripts of amhy were detected in embryos from late blastula stage until hatching in all amhy+/− individuals (Fig. 2B). In larvae trunks, the expression of amhy was highest at 1 wah and decreased until 4 wah, when it reached a low but stable plateau (Fig. 3A). amha mRNA expression was undetectable in amhy+/− embryos (Fig. 2B) and low in larvae between 1 and 3 wah (Fig. 3B) but clearly upregulated between 4 and 6 wah. amha mRNA expression was not detected in any of the amhy−/− embryos (Fig. 2B) and was consistently low in larvae between 1 and 3 wah (Fig. 3C). In contrast, between 4 and 10 wah the mRNA expression assumed a bimodal distribution thereby 7 out of 19 amhy−/− individuals (37%) had high values and the remaining ones low levels (Fig. 3C).

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Figure 2. Expression of amhy and amha mRNAs in tissues and embryos.

A: Tissue distribution of amhy and amha mRNAs in juvenile pejerrey (RT-PCR). B: Expression profile of amhy and amha during embryogenesis in amhy+/− and amhy−/− genotypes (RT-PCR). β-actin was used as endogenous control. NC: negative control.

https://doi.org/10.1371/journal.pone.0102574.g002

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Figure 3. Quantification of amhy, amha and cyp19a1a mRNAs during sex differentiation.

A to C: Abundance of mRNA transcripts of amhy (A) and amha (B) in amhy+/− genotypes and of amha in amhy−/− genotypes (C) during larval development at 25°C (n = 3 to 6 per time point; qRT-PCR). D: Abundance of amha mRNA transcripts in relation to cyp19a1a in amhy+/− and amhy−/− genotypes at 4 and 6 weeks after hatching (qRT-PCR); arrows indicate two arbitrarily-defined, opposing patterns of gene expression. β-actin was used as endogenous control. Values with different letters are statistically different from one another (One-Way ANOVA with Bonferroni's post-test, p<0.05).

https://doi.org/10.1371/journal.pone.0102574.g003

A comparative analysis between the expression of amha and the ovarian differentiation marker cyp19a1a at 4 and 6 wah revealed that all 10 amhy+/− individuals had high and low transcript levels of amha and cyp19a1a, respectively (Fig. 3D). The amhy−/− animals, on the other hand, showed either this pattern (4 out of 10 individuals) or the opposite one with relatively high cyp19a1a and low amha levels (6 out of 10 individuals; Fig. 3D).

Localization of amha/amhy mRNAs by ISH

ISH signals for amha/amhy were detected exclusively in somatic cells of the medullary region of gonads of all amhy+/− (n = 2 for each sampling point) and in 8 out of 14 amhy−/− individuals from 4 and 10 wah (Fig. 4). At 10 wah, when all gonads had differentiated as ovaries or testes, only the latter had ISH signals.

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Figure 4. Spatial expression of amhy and amha mRNAs in differentiating gonads.

Localization amhy and/or amha transcripts by ISH (left panels) and light microscopic histology (right panels) of gonads in 4 and 10 week old larvae reared at 25°C. Transcripts were detected in all amhy+/− genotypes (presumptive amhy and/or amha signals) and in about half of the amhy−/− genotypes (amha signals). At 10 wah, the expression was detected in developing testis but not in developing ovaries. Scale bars indicate 10 µm.

https://doi.org/10.1371/journal.pone.0102574.g004

Relation of phenotypic sex to amhy genotype under controlled conditions

The remaining fish from the amha/amhy expression analysis at 14 wah (n = 67) were 68.7% males and 31.3% females. The ratio of amhy+/− to amhy−/− fish was nearly 1∶1 (49.3%:50.7%) and all of the formers (n = 33) were phenotypically male. Among the 34 amhy−/− fish, 21 (61.8%) and 13 (38.2%) were female and male, respectively. The gonads of all individuals examined, including the testes of both amhy−/− and amhy+/− males, had no abnormalities or difference of any kind compared to previously reported criteria [2], [19] (data not shown).

Discussion

In this study, we examined whether a homolog of the sex determining gene amhy of Odontesthes hatcheri [8] is present and plays any role in testis determination of pejerrey O. bonariensis, a species otherwise known for its strong temperature-dependent sex determination [1]. Cloning of the O. bonariensis amhy revealed a molecule that is 98% and 97% identical in terms of the open reading frame and TGF-β domain, respectively, to its homolog in O. hatcheri. Wild-caught pejerrey and captive broodstock were then genotyped on the basis of amhy, showing its presence in about half of the individuals and, for those that were phenotypically sexed, with few exceptions, they were males. More importantly, amhy+/− was linked 100% to maleness in a progeny that was reared throughout the critical period of sex determination under a temperature (25°C) known to produce mixed-sex populations [1], [2]. Conversely, most of the amhy−/− individuals were females although there were clearly more exceptions among those reared at 25°C (e.g., approximately 1/3 of amhy−/− males; see further discussion below about the effects of this temperature). In this context, and keeping in mind the strong effects of water temperature on pejerrey sex determination [1], the results suggest that amhy is sex-linked in O. bonariensis and that it could be implicated in the sex determination of this species just as it is in O. hatcheri [8].

To address this hypothesis, we examined the ontogeny of amhy expression during gonadal sex determination and histological sex differentiation in offspring from an amhy−/− female and an amhy+/− male raised under controlled laboratory conditions. During incubation at 19°C, amhy transcripts were consistently expressed from the late-blastula stage onwards in all amhy+/− genotypes. The amhy transcription was maintained through hatching and transfer to 25°C, the period considered as critical for sex determination (1–5 wah) [1], and finally the appearance of histological signs of gonadal differentiation (4–7 wah) [2]. This pattern of expression is consistent with a role in gonadal differentiation and, considering its sex linkage, the cellular pattern of expression described below, as well as the known involvement of Amh in testicular differentiation in several fish species including its congener O. hatcheri [4], [8], [20], with testicular development. Still, the expression from early embryogenesis, even before the formation of the gonad anlagen, is intriguing. This is much earlier than in O. hatcheri where amhy plays the master trigger for testicular differentiation [8]. Whether this early sex-specific expression can affect sex afterwards by epistatic effects on other genes, hence predisposing the amhy+/− genotypes to become males, remains to be assessed. Other questions concerning amhy that must be addressed are to what degree its expression is affected by water temperature, if it acts through or independently of amha (see the following discussion), and if the expression found in the brain is implicated in sex differentiation.

In contrast to amhy, amha was found in all fish regardless of gonadal phenotype, indicating that it is located in autosomal chromosomes just as it is in O. hatcheri [8]. Yet, it seems to be critical for masculinization in amhy−/− individuals, perhaps as a function of temperature and endocrine factors [4], and may be a coadjuvant factor in amhy+/− genotypes. The first line of evidence that supports a role for amha is that its expression, although not as early as that of amhy, coincided temporally with the period when the pejerrey gonads are still sexually labile (see references above). This pattern differs from the late amha expression described in O. hatcheri, where it is considered as irrelevant for testicular differentiation [8]. Further, both qRT-PCR and ISH revealed a bimodal pattern of amha expression in amhy−/− individuals where the proportion of animals with high amha expression during the estimated period of sex determination (37%) closely approximated the proportion of animals with low cyp19a1a during the same period (40%) and that of phenotypic males determined at 14 wah (38%). Also, when the gonads had clearly differentiated by 10 wah, gonads showing amha expression were testes whereas those without it were ovaries. Finally, all amhy+/− animals had high amha as well as low cyp19a1a transcription during the period of sex determination and all became males.

Taken together, these results strongly suggest that amhy+/− genotypes differentiate as males by expression of either amhy alone or amhy and amha together and that amhy may be implicated in the up regulation of amha. We also hypothesize that amhy−/− genotypes rely on amha expression for testis differentiation. Nevertheless, the actual processes underlying amha regulation in both genotypes remain to be elucidated. In this regard, it must be noted that the TGF-beta domain, the region that binds to the primary receptor AmhrII, is highly conserved in both amhy and amha genes of O. bonariensis as in O. hatcheri [8]. Thus, we suppose that Amha may activate the same AmhrII used by Amhy for the activation of downstream pathway of testis differentiation in amhy−/− genotypes. Ongoing studies are focusing on the thermal thresholds for mRNA expression, receptor binding, and the relative contributions of amhy and amha for masculinization.

The sex ratio in the controlled rearing experiment was significantly (about 70%) male-biased and only female-to-male sex-reversals were noted. This highlights the importance of the discovery of amhy for unbiased and accurate screening of thermal effects on gonadal sex differentiation. Thus, the current results suggest that 25°C might not be exactly neutral for pejerrey in terms of sex effects as previously assumed [1]. Alternatively, other forms of stress may have caused elevation in cortisol levels, which is able to induce testicular differentiation [6], [7], and thus activated the male pathway leading to sex-reversal. Given the results obtained in this study, it could be argued that pejerrey possesses a genotypic sex determinant in spite of having a marked TSD. This finding underscores the difficulty in drawing a line between GSD and TSD and that these forms are likely part of a continuum [21], [22]. On the other hand, it is intriguing how amhy has been maintained in the course of evolution in a species whose sex is highly susceptible to temperature effects. The high thermal dependence of sex associated to the presence of a marker for genetic predisposition of gender makes O. bonariensis a very attractive model to study these issues as well as the molecular pathways of high temperature-induced masculinization and low temperature-induced feminization. Although in low frequency, both amhy+/− females and amhy−/− males were found in a wild population, raising concerns about its causes and the impact of temperature-dependent sex determination and sex-reversals on the population demographics [12]. The finding of amhy will make possible to monitor wild pejerrey populations for mismatches between genotypic and phenotypic sex and may prove instrumental for field studies addressing the effects of endocrine disruptors or abnormal temperatures on reproduction and the ecological relevance of TSD for this species.

In summary, this study demonstrated that the amhy gene is active in amhy+/− genotypes before, during, and after the critical time-window of TSD. Although some amhy−/− individuals developed as males, no amhy+/− females were found among fish reared at intermediate temperatures, suggesting that under similar conditions amhy is a strong determinant of testis differentiation. Taken together, the present results provide strong support for the coexistence of GSD and TSD in O. bonariensis.

Supporting Information

Figure S1.

Quantification of β-actin mRNA during larval development. Abundance of β-actin mRNA transcripts in trunks of larvae reared from 1 to 10 weeks after hatching at 25°C (qRT-PCR). Symbols and bars indicate the means and SEM, respectively. Values with the same letter are not statistically different from one another (One-Way ANOVA with Bonferroni's post-test, p>0.05).

https://doi.org/10.1371/journal.pone.0102574.s001

(TIF)

Table S1.

Details of the primers used for amhy cloning, amhy genotyping and expression analysis with the respective PCR conditions.

https://doi.org/10.1371/journal.pone.0102574.s002

(DOCX)

Table S2.

Proportion of amhy+ and amhy−/− genotypes in the progenies produced by single-pair crosses using laboratory broodstock fish.

https://doi.org/10.1371/journal.pone.0102574.s003

(DOCX)

Acknowledgments

We would like to thank the staffs of Field Science Center, Yoshida Station, Tokyo University of Marine Science and Technology, for kindly supplying the broodstock fish of this study.

Author Contributions

Conceived and designed the experiments: YY RSH CAS. Performed the experiments: YZ MS. Analyzed the data: YY RSH. Wrote the paper: YY RSH CAS.

References

  1. 1. Strüssmann CA, Saito T, Usui M, Yamada H, Takashima F (1997) Thermal thresholds and critical period of thermolabile sex determination in two atherinid fishes, Odontesthes bonariensis and Patagonina hatcheri. J Exp Zool 278: 167–177.
  2. 2. Ito LS, Yamashita M, Takashima F, Strüssmann CA (2005) Dynamics and histological characteristics of gonadal sex differentiation in pejerrey (Odontesthes bonariensis) at feminizing and masculinizing temperatures. J Exp Zool 303A: 504–514.
  3. 3. Shinoda T, Miranda LA, Okuma K, Hattori RS, Fernandino JI, et al. (2010) Molecular cloning and expression analysis of Fshr and Lhr in relation to Fshb and Lhb subunits during the period of temperature-dependent sex determination in pejerrey Odontesthes bonariensis. Mol Rep Dev 77: 521–532.
  4. 4. Fernandino JI, Hattori RS, Kimura H, Strüssmann CA, Somoza GM (2008) Expression profile and estrogenic regulation of Anti-Müllerian hormone during gonadal development in pejerrey Odontesthes bonariensis, a teleost fish with strong temperature-dependent sex determination. Dev Dyn 237: 3192–3199.
  5. 5. Fernandino JI, Hattori RS, Shinoda T, Kimura H, Strobl-Mazzulla PH, et al. (2008) Dimorphic expression of dmrt1 and cyp19a1 (ovarian aromatase) during early gonadal development in pejerrey, Odontesthes bonariensis. Sex Dev 2: 316–324.
  6. 6. Hattori RS, Fernandino JI, Kishii A, Kimura H, Kinno T, et al. (2009) Cortisol-induced masculinization: does thermal stress affect gonadal fate in pejerrey, a teleost fish with temperature-dependent sex determination? PLoS ONE 4(8): e6548.
  7. 7. Fernandino JI, Hattori RS, Kishii A, Kimura H, Strobl-Mazzulla PH, et al. (2012) The cortisol and androgen pathways cross talk in high temperature-induced masculinization: the 11β-hydroxysteroid dehydrogenase as a key enzyme. Endocrinology 153: 6003–6011.
  8. 8. Hattori RS, Murai Y, Oura M, Masuda S, Majhi SK, et al. (2012) A Y-linked anti-Müllerian hormone duplication takes over a critical role in sex determination. Proc Natl Acad Sci USA 109: 2955–2959.
  9. 9. Strüssmann CA, Akaba T, Ijima K, Yamaguchi K, Yoshizaki G, et al. (1997) Spontaneous hybridization in the laboratory and genetic markers for the identification of hybrids between two atherinid species, Odontesthes bonariensis (Valenciennes 1835) and Patagonina hatcheri (Eigenmann 1909). Aquacult Res 28: 291–300.
  10. 10. Baroiller JF, Guigen Y, Fostier A (1999) Endocrine and environmental aspects of sex differentiation in fish. Cell Mol Life Sci 55: 910–931.
  11. 11. Devlin RH, Nagahama Y (2002) Sex determination and sex differentiation in fish: an overview of genetic, physiological, and environmental influences. Aquaculture 208: 191–364.
  12. 12. Strüssmann CA, Conover DO, Somoza GM, Miranda LA (2010) Implications of climate change for the reproductive capacity and survival of New World silversides (family Atherinopsidae). J Fish Biol 77: 1818–1834.
  13. 13. Penman DJ, Piferrer F (2008) Fish Gonadogenesis. Part I: Genetic and Environmental Mechanisms of Sex Determination. Rev Fish Sci 16: 16–34.
  14. 14. Baroiller JF, D'Cotta H, Saillant E (2009) Environmental effects on fish sex determination and differentiation. Sex Dev 3: 118–135.
  15. 15. Luckenbach JA, Borski RJ, Daniels HV, Godwin J (2009) Sex determination in flatfishes: mechanisms and environmental influences. Semin Cell Dev Biol 20: 256–263.
  16. 16. Aljanabi SMI, Martinez I (1997) Universal and rapid salt-extraction of high quality genomic DNA for PCR-based techniques. Nucleic Acids Res 25: 4692–4693.
  17. 17. Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4: 406–425.
  18. 18. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, et al. (2011) MEGA5: Molecular Evolutionary Genetics Analysis using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods. Molecular Biology and Evolution 28: 2731–2739.
  19. 19. Strüssmann CA, Ito LS (2005) Where does gonadal sex differentiation begin? Gradient of histological sex differentiation in the gonads of pejerrey, Odontesthes bonariensis (Pisces, Atherinidae). J Morphol 265: 190–196.
  20. 20. Piferrer F, Guiguen Y (2008) Fish gonadogenesis. Part II: molecular biology and genomics of sex differentiation. Rev Fish Sci 16: 35–55.
  21. 21. Strüssmann CA, Patiño R (1999) Sex determination, Environmental. In: Knobil E, Neill JD, editors. Encyclopedia of Reproduction. San Diego: Academic Press. pp. 402–409.
  22. 22. Barske LA, Capel B (2008) Blurring the edges in vertebrate sex determination. Curr Opin Genet Dev 18: 499–505.