TY - JOUR
T1 - Enabling comparative gene expression studies of thyroid hormone action through the development of a flexible real-time quantitative PCR assay for use across multiple anuran indicator and sentinel species
AU - Veldhoen, Nik
AU - Propper, Catherine R.
AU - Helbing, Caren C.
N1 - Funding Information:
We thank Amanda Carew and Stacey Maher for animal exposures and tissue collection and Taka-Aki Ichu and Vicki Rehaume for help in tissue collection and processing. Expert assistance in TAXISS qPCR assay development and validation was provided by Austin Hammond, Stephanie E. Wolff, Claire Ramirez, Amanda Carew, Mitchel Stevenson, Pola Wojnarowicz, and Austin Eakin. This work was funded by the Northern Arizona University Technology and Research Initiative Fund and NIH Grant no. 5 R25 GM056931-16 to C.R.P. and by the Natural Sciences and Engineering Research Council (Canada) to C.C.H.
PY - 2014/3
Y1 - 2014/3
N2 - Studies performed across diverse frog species have made substantial contributions to our understanding of basic vertebrate development and the natural or anthropogenic environmental factors impacting sensitive life stages. Because, anurans are developmental models, provide ecosystems services, and act as sentinels for the identification of environmental chemical contaminants that interfere with thyroid hormone (TH) action during postembryonic development, there is demand for flexible assessment techniques that can be applied to multiple species. As part of the "thyroid assays across indicator and sentinel species" (TAXISS) initiative, we have designed and validated a series of cross-species real time quantitative PCR (qPCR) primer sets that provide information on transcriptome components in evolutionarily distant anurans. Validation for fifteen gene transcripts involved a rigorous three-tiered quality control within tissue/development-specific contexts. Assay performance was confirmed on multiple tissues (tail fin, liver, brain, and intestine) of Rana catesbeiana and Xenopus laevis tadpoles enabling comparisons between tissues and generation of response profiles to exogenous TH. This revealed notable differences in TH-responsive gene transcripts including thra, thrb, thibz, klf9, col1a2, fn1, plp1, mmp2, timm50, otc, and dio2, suggesting differential regulation and susceptibility to contaminant effects. Evidence for the applicability of the TAXISS anuran qPCR assay across seven other species is also provided with five frog families represented and its utility in defining genome structure was demonstrated. This novel validated approach will enable meaningful comparative studies between frog species and aid in extending knowledge of developmental regulatory pathways and the impact of environmental factors on TH signaling in frog species for which little or no genetic information is currently available.
AB - Studies performed across diverse frog species have made substantial contributions to our understanding of basic vertebrate development and the natural or anthropogenic environmental factors impacting sensitive life stages. Because, anurans are developmental models, provide ecosystems services, and act as sentinels for the identification of environmental chemical contaminants that interfere with thyroid hormone (TH) action during postembryonic development, there is demand for flexible assessment techniques that can be applied to multiple species. As part of the "thyroid assays across indicator and sentinel species" (TAXISS) initiative, we have designed and validated a series of cross-species real time quantitative PCR (qPCR) primer sets that provide information on transcriptome components in evolutionarily distant anurans. Validation for fifteen gene transcripts involved a rigorous three-tiered quality control within tissue/development-specific contexts. Assay performance was confirmed on multiple tissues (tail fin, liver, brain, and intestine) of Rana catesbeiana and Xenopus laevis tadpoles enabling comparisons between tissues and generation of response profiles to exogenous TH. This revealed notable differences in TH-responsive gene transcripts including thra, thrb, thibz, klf9, col1a2, fn1, plp1, mmp2, timm50, otc, and dio2, suggesting differential regulation and susceptibility to contaminant effects. Evidence for the applicability of the TAXISS anuran qPCR assay across seven other species is also provided with five frog families represented and its utility in defining genome structure was demonstrated. This novel validated approach will enable meaningful comparative studies between frog species and aid in extending knowledge of developmental regulatory pathways and the impact of environmental factors on TH signaling in frog species for which little or no genetic information is currently available.
KW - Anuran
KW - Frog tadpole
KW - Metamorphosis
KW - Multispecies assay
KW - Normalizer
KW - Quantitative PCR
KW - Thyroid hormone
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U2 - 10.1016/j.aquatox.2014.01.008
DO - 10.1016/j.aquatox.2014.01.008
M3 - Article
C2 - 24503578
AN - SCOPUS:84893485028
SN - 0166-445X
VL - 148
SP - 162
EP - 173
JO - Aquatic Toxicology
JF - Aquatic Toxicology
ER -