Octylphenol and UV-B radiation alter larval development and hypothalamic gene expression in the leopard frog (Rana pipiens). (Articles).

We assessed octylphenol (OP), an estrogenic endocrine-disrupting chemical, and UV-B radiation, a known stressor in amphibian development, for their effects on hypothalamic gene expression and premetamorphic development in the leopard frog (Rana pipiens). Newly hatched tadpoles were exposed for 10 days to OP alone at two different dose levels; to subambient UV-B radiation alone; and to two combinations of OP and UV-B. Control animals were exposed to ethanol vehicle (0.01%) exposure, a subset of tadpoles from each treatment group was raised to metamorphosis to assess differences in body weight and time required for hindlimb emergence. Tadpoles from one of the OP/UV-B combination groups had greater body weight and earlier hindlimb emergence (p < 0.05), but neither OP nor UV-B alone produced significant changes in body weight or hindlimb emergence, indicating a potential mechanism of interaction between OP and UV-B. We hypothesized that the developing hypothalamus might be a potential environmental sensor for neurotoxicologic studies because of its role in the endocrine control of metamorphosis. We used a differential display strategy to identify candidate genes differentially expressed in the hypothalamic region of the exposed tadpoles. Homology cloning was performed to obtain R. pipiens glutamate decarboxylases--GAD65 and GAD67, enzymes involved in the synthesis of the neurotransmitter [gamma]-aminobutyric acid (GABA). cDNA expression profiles revealed that OP and UV-B affected the levels of several candidate transcripts in tadpole (i.e., Nck, Ash, and phospholipase C [gamma]-binding protein 4 and brain angiogenesis inhibitor-3) and metamorph (i.e., GAD67, cytochrome C oxidase, and brain angiogenesis inhibitor-2 and -3) brains. This study represents a novel approach in toxicology that combines physiologic and molecular end points and indicates that levels of OP commonly found in the environment and subambient levels of UV-B alter the expression of important hypothalamic genes and disrupt tadpole growth patterns. Key words: amphibians, angiogenesis, endocrine-disrupting chemicals, estradiol, frogs, GABA, hypothalamus, Rana pipiens.

http://ehpnet1.niehs.nih.gov/docs/2002/110p277-284crump/abstract.html

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The presence of an increasing number of endocrine-disrupting chemicals (EDCs) in the environment may result in chronic exposure of humans and wildlife to low concentrations of contaminants including pesticides (e.g., dichlorodiphenyltrichloroethane, methoxychlor), polychlorinated biphenyls, synthetic steroids (e.g., ethinylestradiol), and some alkylphenolic compounds such as octylphenol (OP). Among wildlife species, the focus of research on EDC exposure has been on animals associated with wetlands or aquatic habitats receiving contaminated effluent and agricultural runoff, in which pollutant exposure has been linked to endocrine disruption (1-4). For example, developing alligator embryos collected from sites contamined with p,p'-dichlorodiphenyldichloroethene and 1,1'-(2,2-dichloroethylidene) bis [4-chlorobenzene] displayed altered sex determination, gonadal steroidogenesis, cliterophallus size, and endocrine or reproductive organ morphology (1). It has been hypothesized that exposure of amphibians to pollutants may disrupt endocrine systems controlling metamorphosis, stress response, and sexual development (5-10). Exposure to UV-B radiation (280-320 nm) has also been found to disrupt development in several amphibian species (11-15). The vulnerability of amphibian species to environmental stressors such as EDCs and UV-B may be associated with amphibian population declines that have been occurring worldwide since the 1960s (16).

In a report on environmental endocrine disruption, the U.S. Environmental Protection Agency suggested that amphibians might be good sentinel animal models for laboratory and field exposure studies (17). Several EDCs, including OP, can displace radiolabeled 17-[beta] estradiol ([[sup.3.H][E.sub.2]) from the estrogen receptor (18), cause significant feminization at low concentrations (e.g., 10 nM OP), and stimulate vitellogenin (VTG) mRNA expression in cultured hepatocytes in Xenopus frogs (9). Reeder et al. (6) reported a weak association (p = 0.07) between the detection of the herbicide atrazine and the prevalence of intersex individuals of the cricket frog (Acris crepitans). These authors also found that sex ratios favored males in juvenile A. crepitans collected from sites contaminated by polychlorinated biphenyls and polychlorinated dibenzofurans. Nishimura et al. (19) raised X. laevis in water containing different concentrations of [E.sub.2] and observed malformations of the head and abdomen, suppressed organogenesis, and suppressed nervous system development at [10.sup.-5] M. Although the dose Nishimura et al. (19) used exceeds physiologic levels, the findings suggest that estrogen exposure can disrupt brain development. Accelerated metamorphosis was observed after the treatment of Bufo bufo and B. americanus tadpoles with [E.sub.2] (20) and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) (21). Cheek et al. (7) observed that the herbicide acetochlor, in the presence of exogenous thyroid hormone [T.sub.3], disrupted development by accelerating metamorphosis in R. pipiens.

Corticotropin-releasing hormone (CRH) plays a central role in amphibian metamorphosis by stimulating the pituitary-thyroid axis, resulting in elevated [T.sub.3] levels in the blood (22-25). This thyroid-regulating effect of CRH in amphibians is in addition to the well-characterized effects of CRH on adrenocorticotropin hormone (ACTH) release in vertebrates (24). The frog hypothalamus can be stimulated by biotic or abiotic factors in the larval habitat (e.g., pond desiccation) to release the neuropeptide CRH (22). Corticosteroids are also released after exposure to stress and can synergize with [T.sub.3] to accelerate metamorphosis (22). Inhibition of metamorphosis is mediated by hypothalamic neurosecretion of the tripeptide thyrotropin-releasing hormone, which controls the biosynthesis and release of the pituitary hormone prolactin (PRL) (24,26). PRL antagonizes metamorphosis and promotes larval growth leading to larger animals at metamorphosis (24,26). Thyroid status is easily altered by the addition of a variety of hormones or [T.sub.3] synthesis inhibitors to water (23), indicating that the hypothalamo-pituitary-thyroid axis is extremely vulnerable to endocrine disruption. Premature metamorphosis and/or abnormal growth patterns could alter fitness and survivorship in amphibians (27).

Alkylphenol polyethoxylates (APEOs) are a large group of nonionic surfactants in commercial production [approximately 250,000 tons produced per year (28)] that enter the aquatic environment predominantly via sewage treatment plants and pulp and paper mills (3,29,30). Upon discharge, APEOs are rapidly degraded to form relatively stable, hydrophobic metabolites; principally the alkylphenols nonylphenol (NP) and OP. OP and NP are estrogenic and stimulate VTG gene expression in trout hepatocytes, induce growth of several breast cancer cell lines (e.g., MCF-7 and ZR-75), inhibit testicular growth in rainbow trout, cause feminization in Xenopus, and competitively bind to both trout and mouse estrogen receptors (9,29-31). Blazquez et al. (32) found that 1 [micro]M OP caused 50% mortality among immature male goldfish 20 days after exposure. There have been no reports on amphibian toxicity data for OP. Most evidence indicates that regardless of the species model, OP, at concentrations ranging from 0.1 [micro]M to 10 [micro]M, is a biologically active contaminant (30-32). Indeed, there is reason for concern because OP has been found at significant concentrations in fresh water (< 2.0 pM-2.5 nM), sediments (< 0.010-1.8 [micro]g/g dry weight), and sewage treatment plant effluent (0.6-12 nM) and sludge (< 0.005-12.1 [micro]g/g dry weight) in North America (33,34). Waterborne OP levels of approximately 63 nM have been reported in rivers and estuaries in the United Kingdom (35).

Previous studies have shown that UV-B radiation (280-320 nm) can disrupt normal development and hinder hatching success and larval survivorship of many amphibian species (11,12). Severe deformities including lordosis (curvature of the spine), bloating/distension, and abnormal development of the presumptive cornea were common pathologies associated with UV-B exposure (13,14). Ankley et al. (15) reported symmetrical hind-limb ectromelia and ectrodactyly after R. pipiens tadpoles were exposed to low levels (44 [micro]W/[cm.sup.2]) of UV-B. Again, metamorphic alterations of this nature in the wild would likely impair predator avoidance, reproductive success, and overall fitness. UV-B can also potentiate the toxicity of several pesticides and polycyclic aromatic hydrocarbons with respect to amphibian survivorship because of the generation of toxic photometabolites (36,37). Ahel et al. (38) determined the kinetics of OP photolysis in natural waters and calculated a half-life of approximately 10-15 hr. However, the photometabolites of OP were not identified. Bennie (34) noted that OP was relatively resistant to microbial degradation but that the final degradation products were water and carbon dioxide.

In the current study, we used sublethal, nonteratogenic levels of OP and UV-B to determine whether an interaction existed between these two stressors with respect to mRNA expression in the brain and effects on metamorphosis, specifically growth rate and hind-limb emergence (HLE). We focused on the tadpole diencephalon (preoptic/hypothalamic area) because the gene expression program for neural development of this brain region has been characterized (23). In addition, many aspects of hypothalamic function are modulated by sex steroids (32), so we hypothesized that the developing hypothalamus would be an effective and novel environmental sensor for neurotoxicologic studies.

Using a rapid molecular screening technique, we set out to isolate and identify candidate molecules in the hypothalamic region of developing leopard frog (R. pipiens) tadpoles that were differentially regulated by OP and UV-B, alone and in combination, as initially determined using differential display. We performed homology cloning to obtain R. pipiens glutamate decarboxylases GAD65 and GAD67, enzymes involved in the synthesis of the neurotransmitter [gamma]-aminobutyric acid (GABA). We used a multiple-gene dot blot in semiquantitative reverse Northern hybridization experiments to determine the extent to which the expression patterns of candidate molecules were altered after treatment with OP and UV-B. We also studied the potential interaction between OP and UV-B on gene expression profiles.

Materials and Methods

Animals and rearing conditions. Two experiments were conducted with animals from different sources. For experiment 1 (30 January 1999) we used animals from an induced breeding event to isolate candidate differentially expressed molecules from tadpole brains. For experiment 2 (2 May 1999) we used animals from naturally fertilized eggs to isolate candidate differentially expressed molecules from metamorph brains. We also assessed growth and premetamorphic development.

Adult R. pipiens were purchased from a commercial supplier (Charles Sullivan & Co., Nashville, TN, USA) and housed in a flow-through aquarium with dry land refuge areas at 18 [degrees] C. They were fed mealworms with Reptovit vitamin supplement (Terrafauna, Morris Plains, NJ, USA). For males and females, breeding was induced in mid-January 1999 by two injections of des-[Gly.sup.10] [D-His [(Bzl).sup.6]]-luteinizing hormone-releasing hormone ethylamide (Sigma, St. Louis, MO, USA) 4 days apart at a dose rate of 50 ng/g in frog saline (0.6% NaCl). Fertilized eggs were maintained in polystyrene containers with aerated, filtered water (pH 7.0; dissolved oxygen 8.4-10 mg/L; 16.5-18 [degrees] C) until stage 21 (39), after which they were distributed to the respective treatment exposures (experiment 1). In addition we collected two broods of naturally fertilized R. pipiens eggs on 29 April 1999 from a typical breeding pond on the campus of Trent University, Peterborough, Ontario (44 [degrees] 22' N, 78 [degrees] 17' W) and used them in experiment 2. All animal experimentation followed the standards and guidelines of the Canadian Council of Animal Care (40).

Conditions of exposure. We conducted a preliminary experiment to determine the 7-day [LC.sub.50] (50% lethal concentration) for R. pipiens tadpoles. This was important so that subsequent exposures would be sublethal and environmentally relevant. We conducted experiments 1 and 2 under the same OP/UV-B regimes, and they lasted for 10 days. Fifteen tadpoles were reared in each 100 x 15 mm Pyrex petri dish (working volume 100 mL) and exposed in a controlled environmental chamber (18 [degrees] C; 12:12 hr light:dark photoperiod) to two concentrations of the environmental estrogen OP (1 nM, 1 [micro]M; groups O[P.sub.1] and O[P.sub.2], respectively), a subambient level of UV-B radiation (7 [micro]W/[cm.sup.2]; group UV), and their combinations, groups UVO[P.sub.1] and UVO[P.sub.2]. In addition, an extra group receiving 0.01% ethanol served as a control. We prepared OP stock solutions (20.6 [micro]g/mL, 20.6 ng/mL) by dissolving 99% pure technical grade 4-OP (Aldrich Chemical Co., Milwaukee, WI, USA) in 95% ethanol. We prepared the nominal concentrations by adding 100 [micro]L of the appropriate OP stock solution to 1 L filtered water. Control and UV-B-only groups were treated with a 0.01% ethanol vehicle. The water was replaced every 48 hr during the study.

The supplemental lighting consisted of UV-B (UBL FS20T12/UVB-BP) and UV-A (combination of Cool White Sylvania F20T12 CW and NEC T10 Black Light Blue) lamps, as well as background laboratory lighting supplied by full spectrum bulbs (Verilux F40T12VLX; both from Sylvania, Mississauga, ON, Canada). Light panels (4 feet long) were positioned above the exposure containers to attain 7 [micro]W/[cm.sup.2] UV-B. These are subambient levels because summer levels of ambient UV-B in eastern Ontario vary between 100 and 250 [micro]W/[cm.sup.2] (12,41). The UV lamps were on for 6 hr per day (1000-1600 hr), and UV measurements were carried out using an Oriel GOLDILUX UV meter with interchangeable UV-B and UV-A probes (ThermoOriel, Stratford, CT, USA).

The experiments were performed with four replicates per treatment. Each petri dish had 15 tadpoles that were fed Nutrafin fish flakes (Rolf C. Hagen, Montreal, Canada) daily ad libitum as of stage 24 [day 5 of the exposure (39)]. After the 10-day exposure, tadpoles from experiment 1 were anesthetized using MS222 (Sigma), and the diencephalon, which contains the developing preoptic/hypothalamic area, was rapidly dissected and frozen on dry ice for subsequent isolation of poly [(A).sup.+]RNA. To obtain sufficient tissue, we pooled diencephalons from 10 tadpoles in each of four independent replicates per treatment.

Postexposure developmental effects. After experiment 2 (12 May 1999), 20 tadpoles [stage 25 (39)], from a total of 60, were randomly selected from each of the 6 experimental groups and transferred into clean water in 4.5-L grow-out containers to monitor premetamorphic growth and development. The tadpoles were kept in a separate environmental chamber with no background UV-B under a 12:12 hr light:dark photoperiod supplied by full spectrum lamps (1-2 [micro]W/[cm.sup.2] UV-A) and a constant temperature of 18 [+ or -] 1 [degrees] C. To minimize density stress during tadpole development, we used two containers per group. Tadpoles were fed ad libitum daily, and overall health was monitored. Two months after the initial 10-day exposure (16 July 1999) stage, 29 tadpoles (39) were weighed to assess potential treatment-related differences in body weight. The onset of HLE, defined as stage 36 (39), of individual tadpoles was also documented daily. At metamorphic climax (tail resorption), hypothalami were rapidly dissected and frozen on dry ice for isolation of poly[(A).sup.+]RNA. We combined hypothalamic tissue from two tadpoles in each of four independent replicates per treatment group.

Differential display and transcript identification. The differential display methodology used in this study was similar to our previously reported strategy (42). Poly(A)+RNA from diencephalons from all treatments of experiment 1 and metamorph hypothalami from all treatments of experiment 2 was isolated using the Straight A's mRNA isolation system (Novagen, Madison, WI, USA) and 100 ng was reverse transcribed using Superscript II (Gibco, Gaithersburg, MD, USA) to cDNA using one of three single 18-base arbitrary primers (primer [A.sub.3]: 5'-AATCTAGAGCTCTCCTGG-3'; primer [B.sub.3]: 5'-CATACACGCGTATACTGG-3'; primer [C.sub.3]: 5'-CCATGCGCATGCATGAGA-3'). The resulting cDNAs were then amplified by polymerase chain reaction (PCR) in the presence of high specific-activity radiolabeled nucleotides ([[sup.32]P]dCTP; 10 mCi/mL) and the original primer used for cDNA first-strand synthesis. Amplification was carried out in a thermocycler with a single cycle of low-stringency amplification (94 [degrees] C, 1 min/36 [degrees] C, 5 min/72 [degrees] C, 5 min) followed by 40 cycles with higher stringency [94 [degrees] C, 1 min/54 [degrees] C (for primers [A.sub.3] and [B.sub.3]); 56 [degrees] C (for primer [C.sub.3]), 2 min/72 [degrees] C, 2 min]. We separated and reamplified PCR products following Blazquez et al. (42). Of approximately 50 bands on the differential display gel, only those few transcripts that displayed an unequivocal presence/absence pattern in the various OP and UV-B treatments were considered differentially regulated. The differentially expressed transcripts were cloned into a pCR II-TOPO vector and transformed in E. coli competent cells using the TOPO TA Cloning Kit (Invitrogen, Groningen, The Netherlands). cDNA was sequenced by Canadian Molecular Research Services Inc (Ottawa, Ontario, Canada) using simultaneous bidirectional sequencing reactions with the DYEnamic Cycle Sequencing Kit (US79535) from Amersham Pharmacia Biotech (Baie d'Urfe, Quebec, Canada) and IRD700 and IRD800 labeled vector primers (LiCor, Lincoln, NE, USA) flanking the DNA insertion site. The sequencing reactions were separated on a LiCor 4200L sequencer and analyzed with Sequencer 4.0 (Gene Codes Corporation, Ann Arbor, MI, USA). Sequence results were compared to known sequences available in GenBank using the BLAST search accessible through the National Center for Biotechnology Information (43).

Reverse Northern multiple-gene dot blot. We used the reverse Northern technique, considered to be semiquantitative (44,45), to detect changes in the abundance of the mRNA transcripts isolated by differential display and homology cloning. Poly(A)+RNA was purified from brain tissue collected during experiment 2 using the Straight A's mRNA isolation system (Novagen), and 200 ng was reverse transcribed following the methods of Parfett et al. (44), except that Superscript II (Gibco) was used in place of M-MLV reverse transcriptase. For this experiment, we used only brain tissues from the low level of OP (1 nM) and UV-B, alone and in combination, and the solvent control. We synthesized second-strand cDNA in the same salts/buffer mixture as the first-strand, and the 50 [micro]L reaction mix contained 1.5 [micro]L fresh deoxynucleotide triphosphates (10 mM), 1 [micro]l bovine serum albumin (BSA; 0.1 [micro]g/[micro]L), 0.5 [micro]L RNAse H (0.027 U/[micro]L), and 0.5 [micro]L E. coli DNA polymerase holoenzyme I (0.1 U/[micro]L. The second-strand cDNA was incubated at 15 [degrees] C for 1 hr, extracted with phenol, and precipitated with ethanol. Probe synthesis consisted of labeling 100 ng of double-stranded DNA with [[sup.32]P]dCTP using the Amersham Pharmacia random primer/T7 DNA polymerase oligo-labeling kit.

We chose a composite selection of seven candidate genes isolated by differential display from both tadpole and metamorph brains for the multiple-gene dot blot. Very few brain-specific molecules of any class have been cloned from the leopard frog. Thus the differential display strategy allowed for rapid isolation of candidate genes altered by UV-B and OP. In addition, the two isoforms of leopard frog glutamate decarboxylase [accession numbers AF202124 (GAD67); AF202125 (GAD65); Trudeau et al. (46)] and snapping turtle (Chelydra serpentina) [beta]-actin (100% identical at the predicted amino acid level with Xenopus [beta]-actin) were included, giving a total of 10 genes. To isolate approximately 30 lag of purified cDNA insert required for the dot blots, the Qiagen Plasmid Maxi Kit (Qiagen, Mississauga, ON, Canada) was used. cDNA inserts were digested with EcoRI (Gibco) and extracted from 1% agarose gels using the QIAquick gel extraction kit (Qiagen). Purified cDNA [300 ng/dot prepared in 240 pL 12 x standard sodium citrate (SSC)] of each of the 10 molecules was dotted, in triplicate, onto Hybond-N+ membranes (Amersham Pharmacia), producing a 10 x 3 gene array. Dot blots were made using a 96-well Schleicher and Schuell apparatus. Dot blots were hybridized (44) for 48 hr at 55 [degrees] C with denatured, [[sup.32]P]-labeled double-stranded cDNA synthesized from poly[(A).sub.+]RNA from the various treatment groups to detect changes in the relative abundance of the 10 mRNA species.

After hybridization, membranes were sequentially washed for 30 rain from low [2 x SSC/0.1% sodium dodecyl sulfate (SDS) at 55 [degrees] C] to high stringency (0.1 x SSC/0.1% SDS at 55 [degrees] C), and specific hybridization signals were visualized with the BioRad phosphor-imaging system and quantified using Quantity One software (BioRad Laboratories, Hercules, CA, USA). All data were normalized to [beta]-actin, as it did not change with OP or UV-B treatments.

Statistical analysis of data. We used linear interpolation to estimate the L[C.sub.50] value. The line between the two nearest concentrations that produced mortality levels above and below 50% was used in the calculation. We analyzed tadpole weight and age at HLE using a two-way analysis of variance (ANOVA). A post-hoc Fisher's least significant difference (LSD) multiple comparisons test was performed to identify differences between treatment groups. The average of internal triplicates on one membrane was calculated per dot blot, and each treatment group had an independent replicate of three or four blots (n = 3 or 4) to ensure reproducibility. Gene expression data were not normal, so we used Friedman's test (a two-way ANOVA on the ranked data) to test for significant interactions between OP and UV-B with respect to mRNA expression (47). This was followed by Fisher's LSD test to determine differences between groups (47). For all statistical procedures, group means were considered different if p < 0.05. As indicated, gene expression data were nonparametric and therefore the median rather than the mean of each treatment group has been presented (47). We used Systat 7.0.1 software (SPSS Inc., Chicago, IL, USA) for all statistical procedures.

Results

L[C.sub.50] for OP

The calculated 7-day L[C.sub.50] value for waterborne OP was 2.8 [micro]M (Figure 1). Figure 1 shows that the toxic response was extremely abrupt: At 2.5 [micro]M there was minimal mortality, and at 3 [micro]M there was 84% mortality. The R. pipiens tadpoles exposed to 1 [micro]M OP in this study displayed minimal (approximately 5%) mortality (Figure 1), and, subsequently, the levels of OP used were at or below 1 [micro]M. No additional increases in mortality were observed in the 1 [micro]M group between 7 and 10 days (data not shown). The ethanol-exposed control group displayed an extremely low mortality rate of approximately 2% (Figure 1).

[FIGURE 1 OMITTED]

Postexposure Developmental Effects

Tadpole body weight (wet weight) at stage 29 (39) changed according to early life-stage exposure. There was no change in weight in animals treated with OP alone (groups O[P.sub.1] and O[P.sub.2]). However, tadpole weight in the UV group was significantly reduced. Moreover, tadpoles treated with a combination of 1 [micro]M OP plus UV-B (group UVO[P.sub.2]) were larger than tadpoles in all other treatments (Figure 2A). Treatments with either OP or UV-B (groups O[P.sub.1], O[P.sub.2], and UV) alone had no effects on the onset of HLE, stage 36 (39). However, tadpoles treated with 1 pM OP plus UV-B (group UVO[P.sub.2]) displayed significant acceleration of HLE compared to all other treatments (Figure 2B).

[FIGURE 2 OMITTED]

Identification of Putative Treatment-Responsive Genes Using Differential Display

Tadpole diencephalon. The differential display strategy identified three candidate cDNA transcripts altered by OP, one transcript altered by UV-B, and two molecules that were unchanged based on a similar band intensity across all treatments (Table 1). The expression of a cDNA fragment (774 bp) approximately 66% identical to the 3' end of human and rat plectin was potentially increased by 1 nM OP. Another transcript (798 bp) that revealed a potential increase in expression following 1 nM OP treatment was 89% identical to human Nck, Ash, and phospholipase C [gamma]-binding protein 4 (NAP4). The expression of a 517-bp transcript was potentially decreased by both 1 nM and 1 [micro]M OP and was 59% identical to human brain-specific angiogenesis inhibitor 2 (BAI2). A 403-bp transcript displayed a potential decrease of expression after UV-B treatment and was 56% identical to rat arcadlin. Finally, the expression of cytochrome C oxidase chain I, an important mitochondrial proton-pumping respiratory protein, and NADH dehydrogenase subunit 4, involved in glycolosis and cellular respiration, appeared to be unchanged across all treatments.

Metamorph hypothalamus. The expression of a 567-bp transcript that was 90% identical to human brain-specific angiogenesis inhibitor 3 (BAI3) was determined to be unchanged based on differential display (Table 1). Differential display also identified a 896-bp fragment in the metamorph hypothalamus that showed a potential increase in expression after exposure to 1 nM and 1 [micro]M OP, alone and in combination with UV-B (groups O[P.sub.1], O[P.sub.2], UVO[P.sub.1], and UVO[P.sub.2], respectively). This molecule was 54% identical to goldfish NADH dehydrogenase subunit 4 (Table 1). Note that the expression of NADH dehydrogenase subunit 4 mRNA was unchanged in the tadpole brain, which suggests a stage- and treatment-specific shift in expression of this molecule.

Determination of Gene Expression Using Reverse Northern Blot Analysis

Tadpole diencephalon. Octylphenol (1 nM; group O[P.sub.1]) induced a 3-fold increase in the expression of NAP4 mRNA (Figure 3A), confirming the initial differential display results (Table 1). All other treatments were without effects (Figure 3A). Although BAI3 mRNA was originally isolated from the hypothalamus of R. pipiens metamorphs, we found that its expression in the tadpole diencephalon was increased 5-fold in animals exposed to UV-B (Figure 3B). All other treatments were without effects (Figure 3B). In addition, we verified that the expression of cytochrome C oxidase chain I and NADH dehydrogenase subunit 4 was unchanged across the various treatment exposures (data not shown). The median values for plectin mRNA expression were not greater in the OP treatment and in fact were similar across all treatments (data not shown). This result, together with those of BAI2 and arcadlin, are inconsistent with the results obtained from the differential display (Table 1). Thus, the reverse Northern experiments confirmed the expression pattern of three of the six transcripts originally isolated from tadpole diencephalon using differential display. A similar level of confidence has been reported for differential display and reverse Northern blots in other vertebrate systems (45). In the tadpole diencephalon, the expressions of GAD65 and GAD67 were similar across all treatments (data not shown).

[FIGURE 3 OMITTED]

Metamorph hypothalamus. GAD67 mRNA levels were not affected by OP (1 nM; group O[P.sub.1]) or UV-B alone. However, the expression of GAD67 mRNA was significantly decreased in the hypothalamus of metamorphs exposed to OP compared to those exposed to UV-B alone. Moreover, GAD67 expression was increased by approximately 2-fold in the hypothalamus of metamorphs coexposed to OP plus UV-B (group UVO[P.sub.1]; Figure 4A). The expression pattern of BAI2 mRNA in the various treatment groups was similar to that observed for GAD67 (Figure 4B). Early exposure to OP (group O[P.sub.1]) resulted in a 2-fold decrease in BAI2 expression, whereas UV-B exposure alone did not affect BAI2 mRNA levels (Figure 4B). In contrast to OP and UV-B treatments alone, the combined OP plus UV-B exposure (group UVO[P.sub.1]) significantly increased BAI2 mRNA expression in the metamorph hypothalamus (Figure 4B). BAI3 was originally determined by differential display to be similarly expressed in all treatment groups (Table 1). However, semi-quantitative reverse Northern blots revealed that UV-B exposure increased BAI3 mRNA expression approximately 3-fold. Similarly, the expression of BAI3 was 4-fold higher in the hypothalamus of animals in group UVO[P.sub.1] than in the control or O[P.sub.1] group (Figure 4C).

[FIGURE 4 OMITTED]

As in the tadpole diencephalon (Figure 3B), BAI3 mRNA levels were increased by UV-B treatment in the metamorph hypothalamus (Figure 4C). As indicated previously, cytochrome C oxidase chain I mRNA was unchanged in the tadpole diencephalon. However, its expression in the metamorph hypothalamus was increased 3-fold in animals exposed to UV-B. In contrast, levels of cytochrome C oxidase chain I mRNA in the hypothalamus of animals treated with OP and OP plus UV-B (groups O[P.sub.1] and UVO[P.sub.1], respectively) were similar to that in controls (Figure 4D). NADH dehydrogenase subunit 4 expression was not regulated (data not shown) as predicted by differential display (Table 1). In addition, mRNA expression of GAD65, plectin, arcadlin, and NAP4 were similar across all treatments (data not shown).

Discussion

The present study shows that an early 10-day exposure of R. pipiens tadpoles to OP and UV-B radiation can disrupt normal premetamorphic development. Body weight before HLE was increased and the day at HLE (i.e., Gosner stage 36) was significantly accelerated by cotreatments of OP plus UV-B. Disruption of metamorphosis has been observed in other amphibian studies when certain toxins (acetochlor, TCDD) were combined with exogenous T3 (7,21). Jung and Walker (21) found that 0.03 [micro]g/L TCDD accelerated metamorphosis and that B. americanus tadpoles exposed to > 0.03 [micro]g/L TCDD had a larger body mass at metamorphosis than vehicle-treated animals. Cheek et al. (7) reported that the herbicide acetochlor ([10.sup.-8] M), in combination with [T.sub.3], accelerated forelimb emergence in R. pipiens. Contrary to the present study, they observed no alteration of tadpole growth or timing of HLE. Cheek et al. (7) proposed that acetochlor enhanced [T.sub.3] action, in the presence of exogenous [T.sub.3], to accelerate a specific metamorphic event, forelimb emergence. The authors further stated that acetochlor might have decreased the enzymatic activity of 5-deiodinase that inactivates [T.sub.4] to [T.sub.3] and [T.sub.3] to [T.sub.2], effectively increasing endogenous [T.sub.3] concentrations and indirectly accelerating metamorphosis.

The mechanisms involved in the changes in metamorphic parameters in this study are currently not well understood. The increase in weight and acceleration of HLE may be the result of a photochemical interaction between OP and UV-B because metamorphic alterations were observed only in this treatment group. The photointermediates of OP have not yet been identified; however, putative photochemical byproducts could conceivably affect the hypothalamo-pituitary-thyroid axis. Hypothalamic release of CRH and the downstream effects on [T.sub.3] concentrations could have been the target in this case, as exogenous [T.sub.3] was not required to observe the metamorphic alterations. Perhaps, as in the study by Cheek et al. (7), the combination of specific stressors accelerates specific metamorphic events. Regardless of the mechanism, physiologic end points such as metamorphosis provide promising indicators of disruption of the hypothalamo-pituitary-thyroid axis (22,48) by environmental contaminants.

Contrary to the laborious techniques of subtractive hybridization and/or library screening, our differential display strategy proved to be an effective method to isolate candidate genes rapidly from the leopard frog, a species whose genome is not characterized. We identified several functionally and structurally important molecules solely by cloning transcripts that displayed a presence/absence pattern in the differential display. These included plectin, an intermediate filament-binding protein that provides mechanical strength and structural integrity to the cytoskeleton (49); NAP4, implicated in coordinating various signaling pathways including growth factor and cell adhesion receptors (50); BAI2 and BAI3, membrane proteins that inhibit neovascularization and act as growth suppressors of glioblastoma (primary brain tumor development) (51); arcadlin, a novel cadherin molecule expressed at the synapses that may play an important role in activity-induced synaptic reorganization underlying long-term memory (52); cytochrome C oxidase chain I, an important mitochondrial proton-pumping respiratory protein; and NADH dehydrogenase subunit 4, involved in glycolosis and cellular respiration. The inclusion of the well-characterized neurotransmitter enzymes GAD65 and GAD67 allowed us to address known hypothalamic pathways in addition to the relatively unknown mechanisms of the candidate molecules.

The effects of OP on growth, metamorphosis, and hypothalamic gene expression observed in this study provide further evidence that OP is a biologically active contaminant at environmentally relevant levels. The 1-nM OP exposure level used in our study is 1,000 times lower than the concentration used in an in vitro culture study where OP (1 [micro]M) induced PRL gene expression in rat pituitary cells (53). Additionally, the 1-nM OP exposure is approximately 2,800 times less than the calculated L[C.sub.50] for R. pipiens tadpoles. The observed effects of UV-B on gene expression are in addition to the well-characterized effects of this stressor on several aspects of amphibian development and survival (11-14).

NAP4 expression was increased by 1 nM OP in the tadpole diencephalon, verifying the pattern observed in the initial differential display. NAP4 is a putative signaling molecule widely expressed in various tissues and during several developmental stages in mammals (50). It contains a complete Src homology region 2 (SH2) domain known to interact with the middle SH3 domain of Nck, an adaptor protein involved in tyrosine kinase-mediated signal transduction for both epidermal and vascular endothelial growth factors (50,54). In addition, Nck affects pathways leading to cellular mitogenesis and morphogenesis (54). During early tadpole development, the diencephalon undergoes substantial restructuring, and the regulation of intercellular communication is essential for proper development and survival (23). In this context, an increase in NAP4 expression after OP treatment could affect important aspects of development of the tadpole brain (e.g., tyrosine kinase-mediated growth factor signal transduction). However, deregulation of certain signal transduction pathways associated with cellular proliferation (e.g., Ras GTPases, extracellular signal-related kinase, ERK) can cause various abnormalities including cancer (54). Nck, and thus NAP4, appear to be functionally involved in Ras GTPases and ERK. Thus, a disruption of normal function caused by OP exposure could lead to similar consequences with respect to cellular proliferation in the hypothalamus.

The expression of BAI3 was increased in brain tissue of tadpoles and metamorphs exposed to UV-B and was additionally increased by the combination of OP plus UV-B in the metamorph hypothalamus. The expression of another member of the BAI family, BAI2, was decreased by OP treatment and was increased by the combination of OP plus UV-B in the metamorph hypothalamus. All members of the BAI family, composed thus far of BAI 1, BAI2, and BAI3, contain a seven-span transmembrane region with an extracellular motif recognized by the integrins and sequences corresponding to thrombospondin type I repeats that can inhibit experimental angiogenesis (51). A local balance between stimulators and inhibitors of neovascularization and vasoproliferation controls angiogenesis (51,55). Angiogenesis inhibitors block the signaling of cancer-cell inducers to surrounding blood vessels and inhibit the vasoproliferation necessary for the growth, persistence, and metastasis of solid tumors (55). The regulation of BAI-related molecules may be important for capillary formation and blood supply to the developing hypothalamus during metamorphosis.

NAP4 is also associated with signal transduction events involving inducers of vasoproliferation and has been shown to have an oncogenic role when overexpressed in fibroblasts (54). Although a decrease in expression of either BAI2 or BAI3 was not observed in the tadpole diencephalon, early exposure to OP did decrease BAI2 expression in the metamorph hypothalamus. NAP4 expression was significantly increased by OP in the tadpole diencephalon, which might stimulate signal transduction events that would lead to vasoproliferation and in metamorphs, the endogenous inhibitors of such vasoproliferation appear suppressed. Additionally, UV-B is a known carcinogen, and in both the tadpole diencephalon and metamorph hypothalamus BAI3 expression appears to be sensitive to UV-B treatment, producing a significant increase of expression. The increases in expression of both NAP4 and BAI3 after UV-B exposure could modulate vasoproliferation in the developing tadpole brain, perhaps contributing to disruption of neuroendocrine function.

GAD67 expression in the metamorph hypothalamus was altered after early exposure to OP and UV-B. Both GAD65 and GAD67 mediate the synthesis of GABA, but their distribution in the brain suggests divergent functional roles (56). GABA is the primary inhibitory neurotransmitter in the central nervous system and acts to induce membrane hyperpolarizations by binding to postsynaptic GAB[A.sub.A] receptors and presynaptic GAB[A.sub.B] receptors (56). GABA also acts as an important neurotrophic and neurodifferentiating signal molecule during early brain development (57). Interestingly, the gene expression pattern of BAI2 is similar to that of GAD67 in metamorph hypothalami, suggesting possible relationships between angiogenesis and GABA neurons during metamorphic development of the hypothalamus.

GABA is found throughout the hypothalamus and regulates most aspects of hypothalamic function (58). GABA has both stimulatory and inhibitory effects on thyrotropin (TSH) release in mammals (58). It has also been shown that GABA inhibits PRL release in both fish and mammals (58,59). In ovariectomized rats, GABA lowered plasma TSH via actions on the dopamine system. However, the inhibitory effects of GABA on TSH release were reduced in rats treated with [E.sub.2] and progesterone (58). On the other hand, GABAergic stimulation of TSH release in both males and ovariectomized female rats has also been reported (58). In amphibians, CRH stimulates pituitary TSH release, which in turn enhances thyroid production of [T.sub.3], the hormonal inducer of metamorphosis (24,26). PRL, on the other hand, antagonizes amphibian metamorphosis and promotes larval growth (24,26). Given that cotreatment with OP (1 nM) plus UV-B increases GAD67 mRNA levels and OP (1 [micro]M) plus UV-B advances metamorphosis, there may be a GABAergic component to the control of TSH and/or PRL release in the leopard frog.

We found that the expression of cytochrome C oxidase chain I was increased approximately 3-fold in the metamorph hypothalamus as a result of early exposure to UV-B. This molecule has been shown to be [T.sub.3]-regulated in the Xenopus gene expression program for neural development and thus is associated with changes in the diencephalon during metamorphosis (23). Cytochrome C oxidase is an important mitochondrial proton-pumping respiratory protein that catalyzes the transfer of electrons from cytochrome C to oxygen (23). The extensive brain restructuring involved in metamorphosis and the corresponding metabolic demands during cell proliferation and differentiation would likely require increased energy via the cytochrome C pathway. Denver et al. (23) proposed that the increased expression of cytochrome C oxidase subunit I in tadpoles might be correlated with changes in brain oxidative phosphorylation. The data in our study suggest that UV-B exposure alters the expression of this [T.sub.3]-responsive molecule, indicating an alteration of a standard metabolic pathway in amphibian metamorphosis.

One major question remaining relates to the unexpected alterations of gene expression profiles when UV-B and OP were given together. For example, in the tadpole diencephalon, OP alone induces NAP4 expression, a response that is abolished in the presence of UV-B. Moreover, UV-B induced the expression of BAI3 in the tadpole diencephalon, and this effect was eliminated with cotreatment of OP. These rather complex modulated responses were also apparent in the metamorphs. Both GAD67 and BAI2 were reduced in OP-exposed animals, but not affected by UV-B; yet the cotreatments induced 2- to 3-fold increases in the expression of these molecules in the hypothalamus. Possible mechanisms for this interaction are speculative at best but likely involve complex gene interactions, perhaps as a result of altered metabolic pathways or signal transduction systems. It is clear from our data that UV-B increases cytochrome C gene expression in the metamorph hypothalamus, which could be reasonably expected to affect cytochrome C activity, perhaps affecting cellular metabolism and OP action. Moreover, interactions between signal transduction pathways are known to occur in neuroendocrine systems (60,61) and during embryonic development of the brain and spinal cord (62,63). Although we do not yet know which signaling pathways are involved in the UV-B and OP responses, we hypothesize that there may be an interaction in several downstream signaling mechanisms that could account for our observations. The molecular mechanisms involved should be explored in future work.

In summary, this study represents a novel technique in toxicology that combines physiologic and molecular end points for a species native to North America. The exact mechanism of action of OP and UV-B, alone or in combination, on the expression of the various candidate molecules is not well understood at this time. It is not possible, at present, to establish a cause-and-effect relationship between the observed changes in hypothalamic gene expression and metamorphosis. However, this study provides confirmation that stressors previously determined to affect amphibians can be assessed at a more subtle level and lends precedence for using molecular techniques to address toxicologic questions. This study is also among the first to attempt such work in the frog tadpole.

Recently, there has been an effort to use large-scale or whole-genome approaches to analyze the effects of drugs and toxicants. The standard Northern blot experiments have now been superseded by dot blots and cDNA microarrays, which can simultaneously determine expression patterns of many genes. The regulation of gene expression occurs primarily at the transcriptional level--hence the interest in developing techniques to measure differentially expressed genes via mRNA (64). It is important to recognize that changes at the mRNA level that were determined here using reverse Northern dot blots may not accurately predict the changes in the functional protein. In fact, there is a relatively poor correlation between gene and protein expression, and often the regulation of protein function is at the translational or post-translational level (64). The functional analysis of protein expression would help determine the precise roles of these molecules in the context of amphibian hypothalamic development and metamorphosis. Nevertheless, early life exposure to a persistent EDC and a subambient level of UV-B radiation alters premetamorphic development and regulates the expression of hypothalamic genes important for signal transduction, angiogenesis, and neurotransmitter synthesis.

Table 1. mRNA transcripts (with accession numbers) potentially altered
by 0P and UV-B in the hypothalamic tissue of leopard frog (R. pipiens)
tadpoles and metamorphs as determined using differential display.

Stage, molecule        Functions
(accession no.)

Tadpole
 Plectin (AF279869)    Mechanical strength for cytoskeleton;
                        structural integrity
 NAP4 (AF279870)       Signal transduction;
                        Growth factor action
 BAI2 (AF279868)       Development of glioblastoma

 Arcadlin (AF279872)   Ca2+ signaling;
                        synaptic reorganization
 Cytochrome C oxidase  Mitochondrial respiratory protein;
 chain I (AF279871)     brain oxidative phosphorylation
 NADH dehydrogenase    Glycolosis; cellular respiration
 subunit 4 (AF279867)
Metamorph
 BAI3 (AF279866)       (see BAI2)
 NADH dehydrogenase    Glycolosis;
 subunit 4 (AF279867)   cellular respiration

Stage, molecule        cDNA length   Primer    Percent identity (a)
(accession no.)

Tadpole
 Plectin (AF279869)      774 bp     [C.sub.3]  66 (rat, X59601)
 NAP4 (AF279870)         798 bp     [C.sub.3]  89 (human, PC4427)
 BAI2 (AF279868)         517 bp     [A.sub.3]  59 (human, NP 001694)
 Arcadlin (AF279872)     403 bp     [B.sub.3]  56 (rat, BAA82442)
 Cytochrome C oxidase    676 bp     [B.sub.3]  62 (alligator, AAD09982)
 chain I (AF279871)
 NADH dehydrogenase      898 bp     [A.sub.3]  54 (goldfish, BAA31247)
 subunit 4 (AF279867)
Metamorph
 BAI3 (AF279866)         567 bp     [A.sub.3]  90 (human, NP 001695)
 NADH dehydrogenase      896 bp     [A.sub.3]  54 (goldfish, BAA31247)
 subunit 4 (AF279867)

Stage, molecule           Treatment effects
(accession no.)

Tadpole
 Plectin (AF279869)     O[P.sub.1] [up arrow]

 NAP4 (AF279870)        O[P.sub.1] [up arrow]

 BAI2 (AF279868)       O[P.sub.1] [down arrow]
                       0[P.sub.2] [down arrow]
 Arcadlin (AF279872)       UV [down arrow]

 Cytochrome C oxidase         No change
 chain I (AF279871)
 NADH dehydrogenase           No change
 subunit 4 (AF279867)
Metamorph
 BAI3 (AF279866)              No change
 NADH dehydrogenase      All treatments [up
 subunit 4 (AF279867)   arrow] except control

Treatments were O[P.sub.1] (1 nM), 0[P.sub.2] (1 [micro]M), and UV
(7 mW/[cm.sup.2]), [up arrow] = increased expression; [down arrow] =
decreased expression.

(a) At the predicted amino acid level; in parentheses is the species
and accession number of the GenBank sequence for the first BLAST
search hit.

REFERENCES AND NOTES

(1.) Guillette LJ Jr, Gross TS, Masson GR, Matter JM, Percival HF, Woodward AR. Developmental abnormalities of the gonad and abnormal sex hormone concentrations in juvenile alligators from contaminated and control lakes in Florida. Environ Health Perspect 102:680-688 (1994).

(2.) Purdom CE, Hardiman PA, Bye VJ, Eno NC, Tyler CR, Sumpter JP. Estrogenic effects of effluents from sewage treatment works. Chem Ecol 8:275-285 (1994).

(3.) Sumpter JP, Jobling S. Vitellogenesis as a biomarker for estrogenic contamination of the aquatic environment. Environ Health Perspect 103(suppl 7):173-178 (1995).

(4.) Folmar LC, Denslow ND, Rao V, Chow M, Crain DA, Enblom J, Marcino J, Guillette LJ Jr. Vitellogenin induction and reduced serum testosterone concentrations in feral male carp (Cyprinus carpio) captured near a major metropolitan sewage treatment plant. Environ Health Perspect 104:1096-1101 (1996).

(5.) Sower SA, Reed KL, Babbitt KJ. Limb malformations and abnormal sex hormone concentrations in frogs. Environ Health Perspect 108:1085-1090 (2000).

(6.) Reeder AL, Foley GL, Nichols DK, Hansen LG, Wikoff B, Faeh S, Eisold J, Wheeler MB, Warner R, Murphy JE, Beasley VR. Forms and prevalence of intersexuality and effects of environmental contaminants on sexuality in cricket frogs (Acris crepitans). Environ Health Perspect 106:261-266 (1998).

(7.) Cheek AO, Ide CF, Bollinger JE, Rider CV, McLachlan JA. Alteration of leopard frog (Rana pipiens) metamorphosis by the herbicide Acetochlor. Arch Environ Contam Toxico 37:70-77 (1999).

(8.) Hopkins WA, Mendonca MT, Congdon JD. Responsiveness of the hypothalamo-pituitary-interrenal axis in an amphibian (Bufo terrestris) exposed to coal combustion wastes. Comp Biochem Physiol C Pharmacol Toxicol Endocrinol 122:191-196 (1999).

(9.) Kloas W, Lutz I, Einspanier R. Amphibians as models to study endocrine disruptors: II. Estrogenic activity of environmental chemicals in vitro and in vivo. Sci Total Environ 225:59-68 (1999).

(10.) Pickford DB, Morris ID. Effects of endocrine-disrupting contaminants on amphibian oogenesis: methoxychlor inhibits progesterone-induced maturation of Xenopus laevis oocytes in vitro. Environ Health Perspect 107:285-292 (1999).

(11.) Blaustein AR, Hoffman PD, Hokit DG, Kiesecker JM, Walls SC, Hays JB. UV repair and resistance to solar UVB in amphibian eggs: a link to population declines? Proc Natl Acad Sci USA 91:1791-1795 (1994).

(12.) Crump D, Berrill M, Coulson D, Lean DRS, McGillivray L, Smith A. Sensitivity of amphibian embryos, tadpoles and larvae to enhanced UV-B radiation in natural pond conditions. Can J Zoo 77:1956-1966 (1999).

(13.) Worrest RC, Kimeldorf DJ. Distortions in amphibian development induced by ultraviolet-B enhancement (290-315nm) of a simulated solar spectrum. Photochem Photobiol 24:377-382 (1976).

(14.) Hays JB, Blaustein AR, Kiesecker JM, Hoffman PD, Pandelova I, Coyle D, Richardson T. Developmental responses of amphibians to solar and artificial UVB sources: a comparative study. Photochem Photobiol 64:449-456 (1996).

(15.) Ankley GT, Tietge JE, DeFoe DL, Jansen KM, Holcombe GW, Durhan EJ, Diamond SA. Effects of ultraviolet light and methoprene on survival and development of Rana pipiens. Environ Toxicol Chem 17:2530-2542 (1998).

(16.) Houlahan JE, Findlay CS, Schmidt DR, Meyer AH, Kuzmin SL. Quantitative evidence for global amphibian declines. Nature 404:752-755 (2000).

(17.) U.S. EPA. Special Report on Environmental Endocrine Disruption: Effects Assessment and Analysis. EPN630/R-96/012. Washington, DC:U.S. Environmental Protection Agency, 1997.

(18.) Lutz I, Kloas W. Amphibians as a model to study endocrine disruptors. I. Environmental pollution and estrogen receptor binding. Sci Total Environ 225:49-57 (1999).

(19.) Nishimura N, Fukazawa Y, Uchiyama H, Iguchi T. Effects of estrogenic hormones on early development of Xenopus laevis. J Exp Zool 278:221-233 (1997).

(20.) Frieden E, Naile B. Biochemistry of amphibian metamorphosis. I. Enhancement of induced metamorphosis by gluco-corticoids. Science 231:37-39 (1955).

(21.) Jung RE, Walker ML. Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on development of anuran amphibians. Environ Tox Chem 16:230-240 (1997).

(22.) Denver RJ. Environmental stress as a developmental cue: corticotropin-releasing hormone is a proximate mediator of adaptive phenotypic plasticity in amphibian metamorphosis. Horm Behav 31:169-179 (1997).

(23.) Denver RJ, Pagvi S, Shi Y. Thyroid hormone-dependent gene expression program for Xenopus neural development. J Biol Chem 272:8179-8188 (1997).

(24.) Denver RJ. The molecular basis of thyroid hormone-dependent central nervous system remodeling during amphibian metamorphosis. Comp Biochem Physiol 119:219-228 (1998).

(25.) Tata JR. Amphibian metamorphosis as a model for studying the developmental actions of thyroid hormone. Biochimie 81:359-366 (1999).

(26.) Tata JR. Amphibian metamorphosis: an exquisite model for hormonal regulation of postembryonic development in vertebrates. Develop Growth Differ 38:223-231 (1996).

(27.) Smith DC. Adult recruitment in Chorus frogs: effects of size and date at metamorphosis. Ecology 68:344-350 (1987).

(28.) Bennett ER, Metcalfe CD. Distribution of alkylphenol compounds in Great Lakes sediments, United States and Canada. Environ Toxicol Chem 17:1230-1235 (1998).

(29.) White R, Jobling S, Hoare SA, Sumpter JP, Parker MG. Environmentally persistent alkylphenolic compounds are estrogenic. Endocrinology 135:175-182 (1994).

(30.) Jobling S, Sheahan D, Osborne JA, Matthiessen P, Sumpter, JP. Inhibition of testicular growth in rainbow trout (Oncorhynchus mykiss) exposed to estrogenic alkylphenolic chemicals. Environ Toxicol Chem 15:194-202 (1996).

(31.) Jobling S, Sumpter JP. Detergent components in sewage effluent are weakly estrogenic to fish: an in vitro study using rainbow trout (Oncorhynchus mykiss) hepatocytes. Aquat Toxico127:361-372 (1993).

(32.) Blazquez M, Bosma PT, Fraser EJ, Van Look KJW, Trudeau VL. Fish as models for the neuroendocrine regulation of reproduction and growth. Comp Biochem Physiol 119:345-364 (1998).

(33.) Lee HB, Peart TE. Determination of 4-nonylphenol in effluent and sludge from sewage treatment plants. Anal Chem 67:1976-1980 (1995).

(34.) Bennie DT. Review of the environmental occurrence of alkylphenols and alkylphenol ethoxylates. Water Qual Res J Can 34:79-122 (1999).

(35.) Blackburn MA, Waldock MJ. Concentrations of alkylphenols in rivers and estuaries in England and Wales. Water Res 29:1623-1629 (1995).

(36.) Hatch AC, Burton Jr, GA. Effects of photoinduced toxicity of fluoranthene on amphibian embryos and larvae. Environ Toxicol Chem 17:1777-1785 (1998).

(37.) Monson PD, Call DJ, Cox DA, Liber K, Ankley GT. Photoinduced toxicity of fluoranthene to northern leopard frogs (Rana pipiens). Environ Toxicol Chem 18:308-312 (1999).

(38.) Ahel M, Scully FE, Hoigne J, Giger W. Photochemical degradation of nonylphenol and nonylphenol polyethoxylates in natural waters. Chemosphere 28:1361-1368 (1994).

(39.) Gosner KL. A simplified table for staging anuran embryos and larvae with notes on identification. Herpetologica 16:183-190 (1960).

(40.) CCAC. Guidelines on: The Care and Use of Wildlife. Ottawa:Canadian Council of Animal Care, 2002.

(41.) Crump D, Lean DRS, Berrill M, Coulson D, Toy L. Spectral irradiance in pond water: influence of water chemistry. Photochem Photobiol 70:893-901 (1999).

(42.) Blazquez M, Bosma PT, Chang JP, Docherty K, Trudeau VL. [gamma]-Aminobutyric acid up-regulates the expression of a novel secretogranin-II messenger ribonucleic acid in the goldfish pituitary. Endocrinology 139:4870-4880 (1998).

(43.) NCBI. Bethesda, MD:National Center for Biotechnology Information. Available: http://www.ncbi.nlm.nih.gov/[cited 25 November 1998].

(44.) Parfett CLJ, Pilon R, Barlow JW, Caldeira AA. Altered abundance of multiple, oxidant-inducible mRNA species in C3H/10T1/2 cells following exposure to asbestos or reactive oxygen species. In Vitro Toxicology 9:403-417 (1996).

(45.) Wan JS, Erlander MG. Cloning differentially expressed genes by using differential display and subtractive hybridization. In: Methods in Molecular Biology, Vol 85: Differential Display Methods and Protocols (Liang P, Pardee AB, eds). Totowa, NJ:Humana Press Inc., 1997;45-68.

(46.) Trudeau VL, Spanswick D, Fraser EJ, Lariviere K, Crump D, Chiu S, MacMillan M, Schulz RW. The role of amino acid neurotransmitters in the regulation of pituitary gonadotropin release in fish. Biochem Cell Biol 78:1-22 (2000).

(47.) Sokal RR, Rohlf FJ. Biometry: The Principles and Practice of Statistics in Biological Research. San Francisco:W.H. Freeman and Co., 1981.

(48.) Crump D. The effects of UV-B radiation and endocrine-disrupting chemicals (EDCs) on the biology of amphibians. Environ Rev 9:61-80 (2001).

(49.) Liu C, Maercker C, Castanon MJ, Hauptmann R, Wiche G. Human plectin: organization of the gene, sequence analysis, and chromosome localization (8q24). Proc Natl Acad Sci USA 93:4278-4283 (1996).

(50.) Matuoka K, Miki H, Takahashi K, Takenawa T. A novel ligand for an SH3 domain of the adaptor protein Nck bears an SH2 domain and nuclear signaling motifs. Biochem Biophys Res Commun 239:488-492 (1997).

(51.) Shiratsuchi T, Nishimori H, Ichise H, Nakamura Y, Tokino T. Cloning and characterization of BAI2 and BAI3, novel genes homologous to brain-specific angiogenesis inhibitor 1 (BAI1). Cytogenet Cell Genet 79:103-108 (1997).

52. Yamagata K, Andreasson KI, Sugiura H, Maru E, Dominique M, Irie Y, Miki N, Hayashi Y, Yoshioka M, Kaneko K, et al. Arcadlin is a neural activity-regulated cadherin involved in long term potentiation. J Biol Chem 274:19473-19479 (1999).

(53.) Abraham EJ, Frawley S. Octylphenol (OP), an environmental estrogen, stimulates prolactin (PRL) gene expression. Life Sci 80:1457-1464 (1997).

(54.) McCarty JH. The Nck SH2/SH3 adaptor protein: a regulator of multiple intracellular signal transduction events. BioEssays 20:913-921 (1998).

(55.) Nishimori H, Shiratsuchi T, Urano T, Kimura Y, Kiyono K, Tatsumi K, Yoshida S, Ono M, Kuwano M, Nakamura Y, et al. A novel brain-specific p53-target gene, BAI1, containing thrombospondin type 1 repeats inhibits experimental angiogenesis. Oncogene 15:2145-2150 (1997).

(56.) Pinal CS, Tobin AJ. Uniqueness and redundancy in GABA production. Perspect Develop Neurobiol 5:109-118 (1998).

(57.) Waagepeterson HS, Sonnewald U, Schousboe A. The GABA Paradox: multiple roles as metabolite, neurotransmitter, and neurodifferentiative agent. J Neurochem 73:1335-1342 (1999).

(58.) McCann SM, Rettori V. The role of gamma amino butyric acid (GABA) in the control of anterior pituitary hormone secretion. In: GABA and Benzodiazepine Receptors (Squires RF, ed). Boca Raton, FL:CRC Press, Inc., 1988;127-130.

(59.) Prunet P, Gonnard JF, Paboeuf G. GABA-ergic control of prolactin release in rainbow trout (Oncorhynchus mykiss) pituitaries in vitro. Fish Physiol Biochem 11:131-137 (1993).

(60.) Burbach JP. Genetic pathways in the developmental specification of hypothalamic neuropeptide and midbrain catecholamine systems. Eur d Pharmacol 405:55-62 (2000).

(61.) Chang JP, Johnson JD, Van Goor F, Wong CJ, Yunker WK, Uretsky AD, Taylor D, Jobin BM, Wong AD, Goldberg JI. Signal transduction mechanisms mediating secretion in goldfish gonadotropes and somatotropes. Biochem Cell Biol 78:139-153 (2000).

(62.) Fritz JL, VanBerkum MF. Calmodulin and son of sevenless dependent signaling pathways regulate midlinecrossing of axons in the Drosophila CNS. Development 127:1991-2000 (2000).

(63.) Jessell TM. Neuronal specification in the spinal cord: inductive signals. Nat Rev Genet 1:20-29 (2000).

(64.) Wildsmith SE, Elcock FJ. Microarrays under the microscope. Mol Pathol 54:8-16 (2001).

Address correspondence to V.L. Trudeau, Department of Biology (CAREG), University of Ottawa, 30 Marie Curie Street, Ottawa, Ontario KIN 6N5, Canada. Telephone: [phone] (ext. 6165). Fax: [phone]. E-mail: vtrudeau@ science.uottawa.ca

We thank C. Parfett and R. Pilon (Health Canada, Ottawa), and S. Chiu (University of Ottawa) for technical expertise. We also acknowledge S. Findlay (University of Ottawa) for advice about statistics and M. Blazquez (University of Aberdeen) and G. Van Der Kraak (University of Guelph) for critically reading the manuscript.

We acknowledge funding support for this project from the Natural Sciences and Engineering Research Council (NSERC; to D.L.) and Canadian Network of Toxicology Centres (to V.L.T). D. Crump received an NSERC graduate scholarship.

Received 1 June 2001; accepted 20 September 2001.