Characterization of the morphological, phenotypic, and molecular effects of 17α- ethynylestradiol...

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Characterization of the morphological, phenotypic, and molecular effects of 17α- ethynylestradiol exposure during early development in Xenopus laevis Amber Tompsett, Steve Wiseman, Eric Higley, Hong Chang John P. Giesy, and Markus Hecker SETAC North America Annual Meeting Portland, OR, USA November 7-11, 2010 Toxicology Centre, University of Saskatchewan

Transcript of Characterization of the morphological, phenotypic, and molecular effects of 17α- ethynylestradiol...

Page 1: Characterization of the morphological, phenotypic, and molecular effects of 17α- ethynylestradiol exposure during early development in Xenopus laevis Amber.

Characterization of the morphological, phenotypic, and molecular effects of 17α-

ethynylestradiol exposure during early development in Xenopus laevis

Amber Tompsett, Steve Wiseman, Eric Higley, Hong Chang John P. Giesy, and Markus Hecker

SETAC North America Annual MeetingPortland, OR, USA

November 7-11, 2010

Toxicology Centre, University of Saskatchewan

Page 2: Characterization of the morphological, phenotypic, and molecular effects of 17α- ethynylestradiol exposure during early development in Xenopus laevis Amber.

Introduction

• Estrogenic chemicals in the environment– Exposure hypothesized to cause adverse effects

• Feminization/demasculinization of males

– Wide variety of species are affected by exposure

• 17α-ethynylestradiol (EE2)– Potent estrogen of environmental concern– Present in oral contraceptives

• Not fully removed by conventional sewage treatment• Detectable in surface water

Page 3: Characterization of the morphological, phenotypic, and molecular effects of 17α- ethynylestradiol exposure during early development in Xenopus laevis Amber.

Introduction

• Xenopus laevis– Common laboratory amphibian– Exquisitely sensitive to estrogenic exposures during

sexual differentiation• Male-to-female phenotypic sex reversal• Recently discovered sex-linked gene

• EE2 and X. laevis used as model systems– Morphological and phenotypic effects of EE2 exposure– Molecular effects underlying sex reversal

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Experimental design

• Dosing Regime*– FETAX control and 0.0025% ethanol solvent control– 0.1, 1, and 10 µg/L EE2

• Tadpole samples– Near sexual differentiation

• Experiment terminated at 96 d– Morphometrics and phenotyping– Molecular samples– Histological samples

*Estrogen equivalent concentrations in surface water normally range from 3-30 ng/L

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Days to Metamorphosis

Survival analysis followed by ANOVA, post-hoc Tukey’s test; significant differences (p<0.05) denoted by different letters

Control Solvent 0.1 ug/L EE2 1 ug/L EE2 10 ug/L EE255

60

65

70

75

80

85

90

Treatment

DTM a a

b

b

b

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Phenotyping: Gross Morphology

Control SC 0.1 ug/L EE2 1 ug/L EE2 10 ug/L EE20

20

40

60

80

100% Male% Female

Treatment

a a

b bb

Fisher’s Exact Tests; significant differences denoted by different letters

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DM-W Based Genotypic Sexing• X. laevis has ZW chromosomal sex determination– ZW female; ZZ male– DM-W resides on the W chromosome

• Multiplex DM-W/DMRT1 PCR genotyping– Genomic DNA– PCR products visualized on a gel

♀♂ DM-W

DMRT1

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Genotypic Sex Ratios

*Initial data from a subsample of EE2 treated animals.

Control SC EE2 Treated*0

10

20

30

40

50

60

70% Male

% Female

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Initial Comparison of Genotyping and Phenotyping

Control P

henotype

Control G

enotype

SC Phenotype

SC Genotype

EE2 Treated Phenotype

EE2 Treated Genotype0

10

20

30

40

50

60

70

80

90

100

% Ambiguous% Female% Male

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2

O

1

O

3T

T

1. Genetic female2. Sex-reversed genetic male3. Genetic male

Gross Phenotypic Morphology

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Transcriptome Analysis

• Nieukwoop-Faber Stage 53 Tadpoles– Undergoing sexual differentiation– Control and 100 µg/L EE2 treated animals• Male genotype

• Illumina Sequencing– RNA Seq– Single-end read– 75 bp read length

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Initial Transcriptome Analysis

• CLC Genomics Workbench– Reads filtered and trimmed– Mapped to X. laevis published mRNAs– Expression analysis

• General Statistics– 70% of reads mapped to an mRNA transcript– 95% of transcripts were detected at least once

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Transcriptome Analysis• Overview of changes

Upregulated at least 2-fold

Downregulated at least 2-fold

Unchanged

73%

12%

15%

22 genes upregulated at least 15-fold66 genes downregulated at least 15-fold

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Types of Genes Impacted

• Up-regulated– Estrogen/steroid hormone metabolism– Cardiac/skeletal muscle contraction and growth– DNA repair

• Down-regulated– Redox metabolic activity– Axonogenesis and synaptogenesis– Metabolism of neurotransmitters

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Potential Genes of Interest

Gene Fold Change

Estrogen sulfotransferase (sult1e1) +19

Frizzled-related protein (frzb-1) +24

Troponin T Type 3 (tnnt3) +37

Cu-Zn superoxide dismutase (sod) -23

Synaptosomal associated protein 25 (snap-25) -85

Sulfotransferase 4a1 (sult4a1) -23

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Biological Relevance of EE2 Exposure

• Male-to-female sex reversal

• May impact individual fitness– Delayed metamorphosis and smaller size

• Changes in the male transcriptome at sexual differentiation– Estrogen/hormone metabolism– Other processes

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Additional Ongoing Analysis

• Histology of gonads– Gross morphology of small

animals unclear

• Parallel wood frog experiment– Native, non-model species

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Acknowledgements

• Toxicology Centre– ETL and ATRF– Jon Doering– Jason Raine

• Canada Research Chairs Program