4.5 Article

Thyroid hormone regulation of mRNAs encoding thyrotropin β-subunit, glycoprotein α-subunit, and thyroid hormone receptors α and β in brain, pituitary gland, liver, and gonads of an adult teleost, Pimephales promelas

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JOURNAL OF ENDOCRINOLOGY
卷 202, 期 1, 页码 43-54

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BIOSCIENTIFICA LTD
DOI: 10.1677/JOE-08-0472

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  1. West Coast Center for Oceans and Human Health (WCCOHH)
  2. NOAA Oceans and Human Health Initiative

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Thyroid hormones (THs) regulate growth, morphological development, and migratory behaviors in teleost fish, yet little is known about the transcriptional dynamics of gene targets for THs in these taxa. Here, we characterized TH regulation of mRNAs encoding thyrotropin subunits and thyroid hormone receptors (TRs) in an adult teleost fish model, the fathead minnow (Pimephales promelas). Breeding pairs of adult minnows were fed diets containing 3,5, 3'-triiodo-L-thyronine (T-3) or the goitrogen methimazole for 10 days. In males and females, dietary intake of exogenous T-3 elevated circulating total T-3, while methimazole depressed plasma levels of total thyroxine (T-4). In both sexes, this methimazole-induced reduction in T-4 led to elevated mRNA abundance for thyrotropin beta-subunit (tsh beta) in the pituitary gland. Fish treated with T-3 had elevated transcript levels for TR isoforms alpha and beta (tr alpha and tr beta) in the liver and brain, but reduced levels of brain mRNA for the immediate-early gene basic transcription factor-binding protein (bteb). In the ovary and testis, exogenous T-3 elevated gene transcripts for tsh beta, glycoprotein hormone alpha-subunit (gph alpha), and tr beta, while not affecting tr alpha levels. Taken together, these results demonstrate negative feedback of T-4 on pituitary tsh beta, identify tr alpha and tr beta as T-3-autoinduced genes in the brain and liver, and provide new evidence that tsh beta, gph alpha, and tr beta are THs regulated in the gonad of teleosts. Adult teleost models are increasingly used to evaluate the endocrine-disrupting effects of chemical contaminants, and our results provide a systemic assessment of TH-responsive genes during that life stage. Journal of Endocrinology (2009) 202, 43-54

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