Potential Contributions of Heat Shock Proteins to Temperature-Dependent Sex Determination in the American AlligatorKohno S.a · Katsu Y.b, c · Urushitani H.b · Ohta Y.d · Iguchi T.b, c · Guillette, Jr. L.J.a
aDepartment of Biology, University of Florida, Gainesville, Fla., USA; bOkazaki Institute for Integrative Bioscience, National Institute for Basic Biology, National Institutes of Natural Sciences, and cDepartment of Basic Biology, The Graduate University for Advanced Studies (SOKENDAI), Okazaki, dLaboratory of Experimental Animals, Department of Veterinary Medicine, Faculty of Agriculture, Tottori University, Tottori, Japan Corresponding Author
Louis J. Guillette, Jr., PhD
Department of Biology
220 Bartram Hall, University of Florida
Gainesville, FL 32611-8525 (USA)
Tel. +1 352 392 1098, Fax +1 352 392 3704, E-Mail firstname.lastname@example.org
Sex determination in the American alligator depends on the incubation temperature experienced during a thermo-sensitive period (TSP), although sex determination can be ‘reversed’ by embryonic exposure to an estrogenic compound. Thus, temperature and estrogenic signals play essential roles during temperature-dependent sex determination (TSD). The genetic basis for TSD is poorly understood, although previous studies observed that many of the genes associated with genetic sex determination (GSD) are expressed in species with TSD. Heat shock proteins (HSPs), good candidates because of their temperature-sensitive expression, have not been examined in regard to TSD but HSPs have the ability to modify steroid receptor function. A number of HSP cDNAs (HSP27, DNAJ, HSP40, HSP47, HSP60, HSP70A, HSP70B, HSP70C, HSP75, HSP90α, HSP90β, and HSP108) as well as cold-inducible RNA binding protein (CIRBP) and HSP-binding protein (HSPBP) were cloned, and expression of their mRNA in the gonadal-adrenal-mesonephros complex (GAM) was investigated. Embryonic and neonatal GAMs exhibited mRNA for all of the HSPs examined during and after the TSP. One-month-old GAMs were separated into 3 portions (gonad, adrenal gland, and mesonephros), and sexual dimorphism in the mRNA expression of gonadal HSP27 (male > female), gonadal HSP70A (male < female), and adrenal HSP90α (male > female) was observed. These findings provide new insights on TSD and suggest that further studies examining the role of HSPs during gonadal development are needed.
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In crocodilians, sex is determined by incubation temperature of the egg during a specific period of embryonic development, the thermo-sensitive period (TSP), rather than by critical sex-determining genes (e.g. SRY) as in mammals [Lang and Andrews, 1994; Morrish and Sinclair, 2002]. Egg incubations at 33.0–33.5°C produce males, whereas egg incubations at 30°C produce females in American alligator [Lang and Andrews, 1994; Milnes et al., 2002]. This system of sex determination is called temperature-dependent sex determination (TSD), and a TSP for TSD has been defined for the American alligator as stages 21–24 [Lang and Andrews, 1994]. Unlike in mammals, estrogens play a central role in the sex determination of fish, birds, crocodilians, and turtles [Crews, 1996; Devlin and Nagahama, 2002]. Indeed, treatment with estrogens or estrogenic compounds during the TSP produces sex reversal in crocodilians or turtles, thus females at male-producing temperatures [Bull et al., 1988; Lance and Bogart, 1994; Crain et al., 1997; Milnes et al., 2002]. Gonadal aromatase (CYP19A1) expression is elevated during and after TSP in alligators and turtles [Smith et al., 1995; Pieau et al., 1999; Gabriel et al., 2001; Murdock and Wibbels, 2003; Pieau and Dorizzi, 2004]. Estrogen receptors (ERs) exist prior to TSP in the genital ridge of the developing red-eared slider turtle and are expressed at a higher density in the future ovary rather than in the testis [Bergeron et al., 1998]. Thus, estrogens are involved in differentiation of an ovary; however, the precise mechanisms and reciprocal actions of estrogens and TSD in reptiles have not been clarified so far.
To date, the expression of several genes known to be important for sex determination in mammals, such as SOX9, anti-müllerian hormone (AMH), WT1, SF1, DAX1, and DMRT1, has been analyzed in alligator gonadal tissue during the TSP [Morrish and Sinclair, 2002]. Endogenous or exogenous estrogen would generate molecular and cellular action through ERs which belong to the nuclear receptor super-family and act as transcription factors. Like birds and mammals, alligators exhibit 2 forms of the nuclear ER, ERα (ESR1) and ERβ (ESR2), which show high sequence similarity to ERs found in other crocodilians, birds, and mammals [Katsu et al., 2004, 2006; Naidoo et al., 2008]. Extensive research on the molecular action of the steroid hormone receptors, including the ERs, indicates that these receptors are part of a transcription complex along with a number of chaperones and cofactors, including the heat shock proteins (HSPs) [Picard, 2006]. Moreover, HSPs were originally identified as the proteins whose expression is induced by heat and other stresses [Lindquist, 1986; Schlesinger, 1994; Ritossa, 1996]. The key factor with the thermo-sensitivity needed to initiate the suite of genetic factors during TSD has not been identified. Therefore, HSPs are interesting candidates to play important roles during the interaction of temperature and estrogen signaling that is known to exist during the TSP. It is also important to recognize that spatially ubiquitous gonadal gene expressions and hormonal signaling would not necessarily drive the morphologically correct differentiation of the gonad; that is, normal morphogenesis requires spatially defined gene expression, thus changes in gonadal morphogenesis, such as the development of basement membranes which would compartmentalize the developing gonad, should also be important in reptilian TSD. For example, germ cells are found in the cortex of undifferentiated gonads, but testis and ovary, respectively, will have germ cells in the medulla and cortex after TSP [Smith and Joss, 1993; Smith and Sinclair, 2004; Yao et al., 2004]. The distribution of germ cells should be one of the critical points for the morphological differentiation in the gonad.
The HSP genes are highly conserved in all eukaryotes and prokaryotes studied to date [Morimoto et al., 1990; Feder and Hofmann, 1999]. Based on sequence homology and the molecular weight of the proteins, the genes have been divided into families such as HSP110, HSP100, HSP90, HSP70, HSP60, HSP40, and the small heat shock proteins, a family of proteins with a molecular weight generally less than 30 kDa [Nover and Scharf, 1997; Gething, 1998; van den Ijssel et al., 1999]. These gene families consist of stress-inducible genes and constitutively expressed genes. In general, inducible genes are expressed at low levels under non-stress conditions, but their expression increases rapidly in response to various stressors. In contrast, basal levels of constitutive genes are high and show relatively little change in the response to stress. However, the inducible and constitutive expression of HSPs is changed during development and cellular differentiation [Craig et al., 1983; Rybczynski and Gilbert, 2000]. HSPs also are induced when a cell or organism undergoes various types of environmental stresses such as heat, cold, desiccation, and oxygen deprivation [Feder and Hofmann, 1999; Kregel, 2002]. The HSP families are grouped according to molecular size, and each family plays various roles in the cells. For example, the HSP90 family works as a chaperone protein for steroid hormone receptors [Pratt, 1997], whereas the HSP70 family is necessary for translocation and protein folding [Gething and Sambrook, 1992], and the HSP60 family is involved in protein stability and folding [Ostermann et al., 1989; Martin et al., 1992].
In the present study, we report the molecular cloning of HSP cDNAs encoding HSP27, DNAJ, HSP40, HSP47, HSP60, HSP70A, HSP70B, HSP70C, HSP75, HSP90α, HSP90β, and HSP108, as well as one cold-inducible RNA-binding protein (CIRBP), and one HSP-binding protein (HSPBP) from the American alligator. Using this sequence information, we built primers allowing us to perform RT-PCR or quantitative real-time PCR in whole GAMs (gonadal-adrenal-mesonephros complexes) or separated GAMs, so we could begin to identify key HSP activities during TSD.
All experiments in this study involving alligators were carried out under the guidelines specified by the Institutional Animal Care and Use Committee at the University of Florida. All fieldwork was performed under permits from the Florida Fish and Wildlife Conservation Commission and the U.S. Fish and Wildlife Service. Alligator eggs were collected from Lake Woodruff National Wildlife Refuge. At least one egg from the clutch was opened to determine embryonic stage based on criteria described by Ferguson . At embryonic stages 19, 24, and 25, eggs incubated at a male-producing temperature (33.5°C) or at female-producing temperature (30.0°C) were opened and GAMs were dissected from the embryos. GAMs were also isolated from neonates (within 48 h after hatching) and one-month-old alligators of both sexes. One animal per each stage was used for RT-PCR analysis to indicate the absence or presence of HSPs in embryonic and neonatal GAM tissue. Embryonic and neonatal sexes were determined by the temperature at which the eggs were incubated and by gross anatomy. They were further confirmed by mRNA expression of AMH and CYP19A1 that are highly sexually dimorphic in the GAM of alligators. At one month of age, GAM tissue from 7 male and 13 female alligators was analyzed; these animals had a mean snout-vent length of 13.9 ± 0.20 cm for males and 13.9 ± 0.15 cm for females. One-month-old animals were sexed by histological analysis and confirmed with mRNA expression of AMH and CYP19A1. GAMs were either flash frozen, fixed in RNAlater (Ambion) or fixed in Bouin’s fixative. Flash frozen GAMs were stored at –70°C, and GAMs fixed in RNAlater were stored at –20°C until analyzed.
Lambda ZAP II cDNA libraries were constructed from stage 25 embryos incubated at male and female-producing temperatures (Stratagene), and cDNAs were randomly sequenced from the 5′-terminal end. Twelve clones encoding the alligator homologs of HSPs, one clone encoding cold-inducible RNA binding protein (CIRBP), and another clone encoding HSP-binding protein (HSPBP) were identified from the cDNA library. In the case of a missing 5′-end of the cDNA it was amplified by 5′-rapid amplification of cDNA end (RACE) using a SMART RACE cDNA Amplification kit (BD Biosciences Clontech). The amplified 5′-end of the cDNA was sequenced and analyzed together with its 3′-side of the cDNA sequence.
All sequences generated were searched for similarity using BLASTN and BLASTP at web servers of the National Center of Biotechnology Information (http://blast.ncbi.nlm.nih.gov/Blast.cgi). All homologous amino acid sequences of Homo sapiens (human), Gallus gallus (chicken), Xenopus laevis (African clawed frog), Danio rerio (zebrafish), Drosophila melanogaster (fruit fly), and Tribolium castaneum (rust-red flour beetle) were used for phylogenetic analysis if the sequence had reference(s). The following sequences were used in the analysis of HSP70s: GenBank accession number were NP_001002012, NP_001006686, NP_001079632, NP_001080064, NP_001080068, NP_001081462, NP_001086039, NP_001091238, NP_001093532, NP_001103873, NP_001107061, NP_001120990, NP_001121147, NP_002146, NP_005336, NP_005337, NP_005338, NP_005518, NP_006588, NP_032327, NP_034608, NP_034609, NP_038586, NP_068814, NP_071705, NP_112442, NP_511132, NP_524063, NP_524339, NP_524356, NP_524474, NP_524798, NP_524927, NP_571472, NP_650209, NP_694881, NP_727563, NP_727564, NP_727565, NP_729940, NP_729941, NP_731651, NP_731716, NP_731987, NP_731988, NP_731989, NP_788663, NP_788679, NP_788680, NP_956908, NP_990334, NP_990822, NP_998223, XP_ 001341446, XP_001811933, XP_001814612, XP_001814746, XP_966611, XP_966842, XP_973521, XP_974442, NP_001006147, NP_001079627, NP_001080166, NP_004125, NP_034611, NP_523741, NP_958483, XP_975386.
GenBank accession numbers for the phylogenetic analysis of HSP90s were NP_001103255, NP_996842, NP_989620, NP_034610, NP_032328, NP_035761, NP_005339, NP_001017963, NP_031381, NP_001085598, NP_001086624, NP_001083114, NP_001084280, NP_571403, NP_001038538, NP_571385, NP_937853, NP_523899, NP_651601, NP_001094067, XP_971540.
Phylogenetic trees for HSP70s and HSP90s were estimated by a web program, Phylogeny.fr [Dereeper et al., 2008], which used the Muscle program for alignments, the Gblocks program for curation, and the PhyML program for phylogeny. The statistical confidence for each branch in the tree was evaluated by aLRT in the PhyML program. Phylogeny was edited on the MEGA4 program [Tamura et al., 2007].
Total RNAs were isolated from GAM tissues using RNeasy (Qiagen). For RT-PCR, 2 µg of total RNA was reverse transcribed using SuperScript III transcriptase (Invitrogen) and oligo (dT) primers. Primer sets used for RT-PCR analyses are shown in table 1. Thirty cycles of amplification were carried out under the following conditions: denaturing at 94°C for 15 s, annealing at 57°C for 30 s, and extension at 72°C for 1 min. At completion, PCR fragments were run on 2% agarose gels. The gel was stained with SYBR Green I (Cambrex), and the gel image was analyzed using a Fluoro-Image Analyzer (FLA-3000G, Fuji Photo Film Co., Ltd.).
After fixation of GAM tissues in Bouin’s fixative, they were dehydrated in a series of graded alcohols (70%, 95%, and 100%), cleared in Citrisol (Fisher Scientific), and embedded in paraffin (Tissue prep 2: Fisher Scientific). GAMs were cross-sectioned at 6 µm and double stained with Alcian Blue and Periodic Acid Schiff (AB-PAS) according to standard methods [Bancroft and Gamble, 2008].
GAMs fixed in RNAlater were carefully partitioned into 3 pieces (gonad, adrenal gland, and mesonephros) under a stereomicroscope. The mesonephros, which had a pigmented line on the lateral surface of the GAM (fig. 1), was isolated first. Second, the gonadal tissue on the ventral surface was isolated, and then the adrenal gland, which was creamy in color, was isolated from the connective tissue of the dorsal side.
Total RNAs were isolated from tissues using a total RNA isolation system (Promega) with a treatment of DNaseI. RNA quantity and quality was verified by measuring its optical density and then running it on an agarose gel. For quantitative real-time PCR (Q-PCR), 1 µg of total RNA was reverse-transcribed in 20 µl of a reaction mix using an iScript cDNA synthesis kit (Bio-Rad). Before starting the analysis, the cDNA was diluted 20-fold with TE buffer, and 1/25 volume of diluted cDNA was used in the Q-PCR analyses as a template. SYBR green-based Q-PCR was performed on a MyiQ Single-Color Real-Time PCR Detection System (Bio-Rad) with AmpliTaq Gold (Applied Biosystems) based homebrew SYBR green reaction mix and the primers for Q-PCR (table 2).
The expression value from each sample was calculated by comparison to standard samples which contained a known concentration of plasmid (copies/µl) ligated for each target. All mRNA expressions were weighted by expression of EEF1A1 mRNA, which was an internal control gene in this study; expressions are presented as weighted mean ± SE. Two-way ANOVA followed by Tukey’s HSD test were used to evaluate differences among tissues and sex and were calculated using JMP version 7.0.2 (SAS Institute Inc.).
After stabilization or fixation of one-month-old GAMs in RNAlater or Bouin’s fixative, the appearance of the GAM was examined (fig. 1). Gonadal tissue was found on the ventral side and was a white structure approximately one fourth of the thickness of the total GAM, whereas the adrenal gland was a creamy, off-white colored tissue lying underneath the gonad. The mesonephros was pigmented by yellow ocher and was found on the lateral surface (fig. 1). As seen in the histology on the right panel of figure 1, it was impossible to cleanly and completely separate one-month-old GAM into 3 portions. The GAMs isolated from one-month-old alligators were, however, carefully dissected under a stereomicroscope and separated into 3 unique portions of tissue largely representative of gonad, adrenal gland, and mesonephros, from which total RNAs were separately isolated, reverse-transcribed, and analyzed in Q-PCR as described in the Methods section.
Fourteen clones encoding alligator homologs ofHSPs (HSP27, DNAJ, HSP40, HSP47, HSP60, HSP70A, HSP70B, HSP70C, HSP75, HSP90α, HSP90β, and HSP108), cold-inducible RNA-binding protein (CIRBP) and HSP-binding protein (HSPBP) were identified following BLAST searches, and their full-length sequences were obtained using the 5′-RACE technique. GenBank Accession numbers were obtained for these American alligator transcripts: HSP27 (AB306274), DNAJ (AB306275), HSP40 (AB306276), HSP47 (AB306277), HSP60 (AB306278), HSP70A (AB306279), HSP70B (AB306280), HSP70C (AB306281), HSP75 (AB306282), HSP90α (AB306283), HSP90β (AB306284), HSP108 (AB306285), CIRBP (AB306286), and HSPBP (AB306287). The cDNA and predicted amino acid sequences of each clone can be found in the GenBank database.
The sequence identity of the majority of the clones, except for the HSP70s and the HSP90s, were analyzed against orthologs from several other species (table 3). Of the clones examined, all were more similar in sequence to chicken than human, Xenopus, or zebrafish, except for CIRBP. Interestingly, HSP40 and HSP60 were highly conserved among alligator, chicken, and human, with percent similarities over 90% in their predicted amino acid sequences. Our data indicate that the alligator CIRBP reported here was more similar to human CIRBP than chicken or Xenopus CIRBP with a similarity to human CIRBP of 91% in amino acid sequence (table 3). Alligator CIRBPwas very similar to dog CIRBP isoform 3, but not isoform 2 (Canis familiaris isoform 2: XM_863507, isoform 3: XM_868601). The overall identities of alligator CIRBP with isoform 2 and isoform 3 of dog CIRBP were 88 and 97%, respectively. Likewise, dog CIRBP isoform 2 revealed a high similarity to chicken CIRBP (94%). These results indicate that alligator CIRBP is likely the ortholog of dog CIRBP isoform 3 and suggests that the alligator could possess another type of CIRBP that is similar to the CIRBP isoform 2 of the dog.
We isolated 3 HSP70 homologs, designated HSP70A, 70B, and 70C. The cDNA encoding the alligator HSP70A homolog consisted of 2,317 bp with an open reading frame (ORF) encoding a 639-amino-acid protein whereas HSP70B has 2,269 bp encoding a protein of 646 amino acids, and HSP70C has 2,788 bp encoding a protein of 672 amino acids. Analysis of sequence similarity indicated that HSP70A was more similar to HSP70B than HSP70C (70A vs. 70B: 86%, 70A vs. 70C: 48%, 70B vs. 70C: 49%; fig. 2A), which was expected as HSP70A and 70B have been reported to belong to the same multigene family. Based on BLAST searches and phylogenetic analysis we found that HSP70A, 70B, and 70C were similar to vertebrate HSP70 protein 2, HSP70 protein 8, and HSP70 protein 9B, respectively (fig. 2B).
The cDNA encoding the alligator HSP90α homolog consisted of 2,957 bp with an ORF that encoded a 728-amino-acid protein, whereas the cDNA encoding the alligator HSP90β homolog had 2,748 bp that encoded a 729-amino-acid protein. In comparison of the amino acid sequences with those of HSP90s from other vertebrate species, alligator HSP90α was more similar to the α-type of HSP90 (93.6%: mouse, 99.0%: chicken, 91.6%: frog) than the β-type (84.5%: mouse, 83.5%: chicken, 83.5%: frog) (table 4). However, the sequence for alligator HSP90α was more closely related to Hsp90β of the zebrafish than the Hsp90α form (Hsp90α: 82.8%, Hsp90β: 84.1%).
The amino acid sequence of alligator HSP90α was very similar to alligator HSP90β (81.8%) (fig. 3A; table 4). The predicted amino acid sequences of alligator HSP90 proteins were similar to each other (81.8%), and the nucleic acid sequences of the coding regions also showed high homology (73.4%, data not shown). However, the sequences of the 3′-untranslated region (3′-UTR) were quite different (fig. 3B; 21.7%). These results were similar to data we obtained following an examination of chicken HSP90 sequence analyses. The sequences of the predicted amino acids and nucleic acids for chicken HSP90α and HSP90β were 82.8 and 73.9% similar to each other, respectively. However, like the alligator, the sequence similarity of the 2 HSP90s of the chicken 3′-UTR was only 23.5%.
HSP90 genes have been analyzed in several vertebrate groups, including mammals, avian, amphibian, and fishes. Further, fly (X03810), nematode (AF461150 for Hetrodera glycines, AJ005784 for Brugia pahangi, Q18688 for Caenorhabditis elegans), scallop (AY362761), and Schistosoma (AY815927) HSP90 genes have also been cloned and their complete sequences determined. Phylogenetic analyses of HSP90 amino acid sequences were generally consistent with existing phylogenetic hypotheses regarding vertebrate and invertebrate relationships, and 2 types of HSP90s were not observed in invertebrates. To better understand the position of alligator HSP90α and β proteins and their reciprocal relationship, a phylogeny was constructed using numerous HSP90 proteins from various vertebrate and invertebrate species (fig. 3C). The results show that alligator HSP90α and HSP90β are similar to vertebrate HSP90α and vertebrate HSP90β, respectively, as would be predicted (fig. 3C).
We hypothesized that temperature-induced sex determination in the alligator could involve temperature-regulated HSP gene expression. This hypothesis, in part, recognizes the role of HSPs as steroid receptor chaperones and cofactors. Steroids, and thus their receptors, appear to play an important role during TSD in the American alligator and other reptiles with this mode of sex determination. To test this hypothesis, we examined the existence of mRNAs of various HSPs. Total RNA was isolated from male and female embryonic GAMs at embryonic stages 19, 24, and 25 and from neonates. All HSPs we cloned were expressed in embryonic and neonatal GAMs isolated from both sexes (fig. 4), although the expression of HSP70A was detectable, but too low to show a band on the gel (data not shown). In female neonatal GAM CYP19A1 mRNA was obviously expressed at a high level, whereas we detected little or no CYP19A1 in male GAM tissue. In contrast, anti-müllerian hormone (AMH) expression was robust in male neonatal GAM but not in female GAM tissue (fig. 4). The expression of these 2 genes, CYP19A1 and AMH, provided robust positive control genes for ovarian and testicular differentiation, respectively.
AMH or CYP19A1 mRNA in one-month-old alligator tissues revealed significant effects of both sex and tissue differences on their expressions levels (fig. 5; table 5). Tissue differences within the GAM were shown for most of the HSP mRNAs examined except for HSP70C and 90α (fig. 5; table 5). The 2 primary factors in this study, sex and tissue type, affected the expression of HSP60, HSP70A, HSP70B, HSP70C, HSP75 and HSP108 mRNA (fig. 5; table 5). Sexually dimorphic patterns were observed in mRNA expression of gonadal HSP27, gonadal HSP70A, and adrenal HSP90α (fig. 5; table 5).
The TSP for TSD is during embryonic stages 21–24 in the American alligator [Ferguson, 1985; Lang and Andrews, 1994]. Although we have not quantified expression levels of HSPs in the GAM during the TSP, the expression of mRNA for various HSPs was verified throughout this period in embryonic GAMs of both sexes.
Heat shock proteins provide a variety of functions in vertebrates, with various classes of HSPs exhibiting different actions [Picard, 2006]. Most of the data collected to date suggest that the steroid hormone receptors are associated with HSP90s in the absence of their specific ligand [Picard, 2006]. The receptor-HSP90 complex is associated with a number of chaperones and cofactors that generate different complexes; i.e., no single form is used to construct the transcription machinery needed for gene expression. Many of the studies of HSP action are based on in vitro biochemical studies of yeast extracts, yet all suggest that 5 components are necessary for the ATP-driven maturation of a steroid receptor-HSP90 complex, those being P23, HSP40, HSP70, HOP, and HSP90 [for review, see Picard, 2006]. Despite observations of HSPs in loggerhead turtles [Harry et al., 1990], no other investigation of the molecular biology of HSPs in reptilian TSD has been reported. Harry et al.  found 42K and 46K proteins in embryonic urinogenital tissue of females, but the proteins were not identified. Our data indicate that all of the components of such a functional complex are present in the developing GAM of the American alligator at TSP. Enticingly, HSP27, HSP70A, and HSP90α revealed sexual dimorphism in mRNA expressions in gonadal or adrenal tissue isolated from one-month-old alligators. These data suggest that an in-depth quantitative analysis of HSP expression and action in embryonic GAM during the TSP is needed.
For example, HSP27 is inducible by environmental stress and developmental changes in mammals [Garrido et al., 2006]. It is involved in the resistance to stress, the organization of cytoplasmic actin, and is translocated from the cytoplasm to the nucleus upon stress induction in mammals [Garrido et al., 2006]. We observed that in one-month-old gonadal tissue from alligators HSP27 mRNA was significantly elevated in testicular tissue when compared to ovarian tissue of the same age. HSP27 can function as a suppressor of estrogen response element (ERE)-mediated transcription by competing with the estrogen receptor (ER) [Chen et al., 2004, 2008]; i.e., estrogenic signaling requires that the ligand (under normal conditions an endogenous estrogen) binds the ER which then dimerizes and translocates to the DNA where it binds to an ERE in the promoter of an estrogen-inducible gene. This process can be modified by various intracellular proteins as they can either complex with the ER machinery to augment or inhibit ERE binding or interact directly with the ERE thus altering estrogenic signaling. HSP27 is capable of suppressing ERE-mediated transcription at the ERE by acting as an intracellular estradiol-binding protein in mammals [Chen et al., 2004, 2008].
The HSP70 family can be divided into 2 subfamilies, a cognate or constitutive type (HSC70) and an inducible form (HSP70). Both of these subfamilies encode proteins that play key roles in the cell as molecular chaperones [Gething and Sambrook, 1992]. In mammalian cells, HSC70 remains unchanged or slightly upregulated upon exposure to environmental and pathological stressors. In contrast, HSP70 is highly induced from low levels, with transcriptional control mediated via heat shock factor 1 that binds in a trimeric form to an HSP70 promoter [Westwood et al., 1991; Kiang and Tsokos, 1998]. The constitutive HSC70 genes are slightly larger than the HSP70 genes, and the carboxyl region of these genes is highly heterogeneous as HSC70 displays a series of unique repeat GGXP motifs and a signature nonapeptide SGPTIEEVD at the N-terminus [Ali et al., 2003; Deane and Woo, 2005]. In the American alligator, HSP70A has 1 GGXP motif and a GGPTIEEVD region, whereas HSP70B has 2 GGXP motifs and a SGPTIEEV region. Alligator HSP70C has neither the GGXP motif nor the N-terminal SGPTIEEVD sequence. These results suggest that alligator HSP70A and 70B belong to the HSC70 family, whereas alligator HSP70C belongs to the HSP70 family. Further characterization of alligator HSP70s should be done using in vivo heat shock or stress experiments to determine whether these HSPs display similar constitutive or inducible patterns as seen in mammals. Our results appear to suggest that a drastic change in HSP70A expression occurs between neonatal and one-month-old time periods, but it is important to note that different primers were used for RT-PCR and Q-PCR as shown in tables 1 and 2. Thus, these results are not directly comparable with each other, and further analyses will be required to understand the potential details of such a change.
HSP70/HSC70 act in various ways including enhancing vitamin D-mediated transcription and its metabolism by working as an intracellular vitamin-D-binding protein [Gacad et al., 1997; Wu et al., 2002]. Vitamin D is an important factor in the synthesis of estrogen in both male and female gonads, as it induces CYP19A1 expression through the vitamin D receptor in mice [Kinuta et al., 2000; Bouillon et al., 2008]. In this study, we observed that neonatal ovarian tissue expressed significantly higher HSP70A and CYP19A1 mRNA levels when compared to testicular tissue of the same age. The enzyme CYP19A1 generates endogenous estrogens, thus being responsible for the transformation of androstenedione or testosterone into estrone or estradiol-17β, respectively. Although it is unlikely that HSP70A is the primary regulatory agent behind the very large difference in CYP19A1 expression when ovarian and testicular tissue is compared, it is possible that this HSP could augment the observed sexual dimorphism by maintaining differentiation of an ovary versus a testis by helping in the upregulation of CYP19A1 expression via vitamin D signaling.
HSP90 proteins are well-conserved molecular chaperones that are involved in signal transduction, protein folding, protein degradation, and morphologic evolution [Chen et al., 2005]. They usually associate with other co-chaperones and play important roles in folding newly synthesized proteins or stabilizing and refolding denatured proteins after stress [Chen et al., 2005]. There are 2 types of HSP90 proteins: HSP90α is an inducible form and HSP90β is a constitutive form in mammals [Chen et al., 2005]. Generally, HSP90 maintains the steroid hormone receptor in an inactive state but keeps it ready to bind its endogenous hormone [Pratt and Toft, 1997]. On the other hand, one isoform of HSP90, HSP90α, has been described to be extracellularly located where it interacts with the matrix metalloproteinase 2 (MMP2) in mammalian cancer cells [Eustace and Jay, 2004; Eustace et al., 2004]. Extracellular HSP90α enhances the invasiveness of cancer cells via regulating MMP2 activities [Eustace et al., 2004]. The degradation of the extracellular matrix by MMPs enhances cell migration that enables carcinoma formation [Nyberg et al., 2006]. The secretion of HSP90α and activation of MMPs does not occur only in cancer cells but also in normal tissues and cells. Prior to the TSP in turtles and crocodilians, when primordial germ cells migrate into the gonad, the germ cells are found at the cortex of undifferentiated gonads [Smith and Joss, 1993; Smith and Sinclair, 2004; Yao et al., 2004]. However, after the TSP and morphogenesis of the testis or ovary in turtles and crocodilians, germ cells lie inside of sex cords (medulla) in males or are outside of sex cords (cortex) in females [Smith and Joss, 1993; Smith and Sinclair, 2004; Yao et al., 2004; Yao and Capel, 2005]. Hence, the location of germ cells changes with gonadal differentiation and potentially is very important for sex determination itself. In our study, male adrenal glands in one-month-old alligators revealed higher expression of HSP90α than adrenals obtained from females. We hypothesize that this could lead to more secretion of HSP90α in the region of the male adrenal gland and the adjacent gonad in male GAMs when compared to females. If this elevated extracellular HSP90α of adrenal origin enhanced MMP2 in the male gonad, it could alter the basement membrane of the sex cords in male gonads providing access for the primordial germ cells. As the result of expressing more adrenal HSP90α in the male, germ cells could migrate into the sex cord through the basement membrane. Although hypothetical, this proposal is testable and helps provide one potential mechanism for the restructuring of the bipotential gonad that occurs during the TSP.
Dax1-deficient mice showed less or weaker basement membranes of seminiferous tubules in testis, whereas the females had multi-oocyte follicles in the ovary [Yu et al., 1998; Jeffs et al., 2001]. These data suggest that one of the functions of DAX1 during sex determination is via the regulation of the structural proteins in the basement membrane. Indeed, the structural protein laminin and its receptor (integrin) play important roles in the migration of primordial germ cells in Drosophila and mice [Jaglarz and Howard, 1995; Anderson et al., 1999]. Structural changes in the extracellular matrix are necessary for cell migration during tissue remodeling, differentiation, and also the TSD. During differentiation, MMP2 could induce cell migration by cleavage of laminin, which is a principal component of the basement membrane [Giannelli et al., 1997]. Additionally, it is well known that the migration of myoid cells into the gonad from the mesonephros is essential for testicular morphogenesis in mammals [Martineau et al., 1997; Tilmann and Capel, 1999; Ross et al., 2003]. Although Yao et al.  could not detect male-specific mesonephric cell migration in the red-eared slider turtle, the structure of the sex cords and the migration of germ cells and/or mesonephric cells is likely important during sex determination in all vertebrates.
In conclusion, our finding that sexual dimorphism exists in mRNA expression of gonadal HSP27, gonadal HSP70A, and adrenal HSP90α suggests that further study is warranted to determine if such factors could be involved in TSD. Like all vertebrates, the alligator gonad is a bipotential gonad prior to sex determination, and the germ cells lie in the cortex. We have highlighted 2 important factors associated with temperature-dependent sex determination, those being (a) estrogen signaling (E2 signal) which is important in the formation of the ovary in most non-mammalian vertebrate species studied to date and (b) the distribution and movement of the germ cells and mesonephric cells in the developing gonad. We observed sexually dimorphic mRNA expression of gonadal HSP27 (male > female), gonadal HSP70A (male < female), and adrenal HSP90α (male > female) in one-month-old alligator tissues. Using these data, we have proposed a hypothesis that needs to be examined in detail in the future (fig. 6). Our hypothesis suggests that gonadal HSP27 can reduce the E2 signal directly at trans-activation, whereas gonadal HSP70A could induce E2 signaling by stimulating vitamin D signaling that leads to the induction of augmented CYP19A1 expression. By working as antagonists, HSP27 and HSP70A could modify E2 signaling which appears to play such a central role in driving gonadal differentiation in alligators (fig. 6). Further, sex determination is not gene expression alone but leads to dramatic changes in gonadal morphology including the location of the germ cells. We hypothesize that adrenal HSP90α is secreted into the extracellular matrix of the adrenal gland and the adjacent gonad altering the basement membrane of the sex cords via activation of the matrix metalloproteinase and thus facilitating the movement of the germ cells and mesonephric cells into the sex cords of the developing testis (fig. 6). Our current findings provide several new observations related to sexually dimorphic gene expression in the alligator gonad and provide insights into TSD, while suggesting a new, albeit simplistic, integrated theory of gene expression, hormonal regulation, and morphological alterations. Future studies must begin to integrate environmental as well as endocrine signaling into a theory that can explain the regulation of the gene networks responsible for the remarkable morphological and physiological transformation associated with gonadal determination and differentiation.
We thank Ms. Rie Ichikawa and Ms. Megumi Hinago for their excellent technical assistance in cDNA cloning. The authors are grateful to the members of the Iguchi and Guillette laboratories for helpful discussions and comments. This work was supported in part by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (Y.K., Y.O., and T.I.), grants from the Ministry of Environment, Japan (Y.K. and T.I.), and grants from UF Opportunity Fund, Howard Hughes Medical Institute Professors program and U.S. NIH (NIEHS R21 ES014053-01) to L.J.G.
Louis J. Guillette, Jr., PhD
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