Identification of Thyroid Hormones and Functional Characterization of Thyroid Hormone Receptor in the Pacific Oyster Crassostrea gigas Provide Insight into Evolution of the Thyroid Hormone System

PLoS One. 2015 Dec 28;10(12):e0144991. doi: 10.1371/journal.pone.0144991. eCollection 2015.

Abstract

Thyroid hormones (THs) play important roles in development, metamorphosis, and metabolism in vertebrates. During the past century, TH functions were regarded as a synapomorphy of vertebrates. More recently, accumulating evidence has gradually convinced us that TH functions also occur in invertebrate chordates. To date, however, TH-related studies in non-chordate invertebrates have been limited. In this study, THs were qualitatively detected by two reliable methods (HPLC and LC/MS) in a well-studied molluscan species, the Pacific oyster Crassostrea gigas. Quantitative measurement of THs during the development of C. gigas showed high TH contents during embryogenesis and that oyster embryos may synthesize THs endogenously. As a first step in elucidating the TH signaling cascade, an ortholog of vertebrate TH receptor (TR), the most critical gene mediating TH effects, was cloned in C. gigas. The sequence of CgTR has conserved DNA-binding and ligand-binding domains that normally characterize these receptors. Experimental results demonstrated that CgTR can repress gene expression through binding to promoters of target genes and can interact with oyster retinoid X receptor. Moreover, CgTR mRNA expression was activated by T4 and the transcriptional activity of CgTR promoter was repressed by unliganded CgTR protein. An atypical thyroid hormone response element (CgDR5) was found in the promoter of CgTR, which was verified by electrophoretic mobility shift assay (EMSA). These results indicated that some of the CgTR function is conserved. However, the EMSA assay showed that DNA binding specificity of CgTR was different from that of the vertebrate TR and experiments with two dual-luciferase reporter systems indicated that l-thyroxine, 3,3',5-triiodothyronine, and triiodothyroacetic acid failed to activate the transcriptional activity of CgTR. This is the first study to functionally characterize TR in mollusks. The presence of THs and the functions of CgTR in mollusks contribute to better understanding of the evolution of the TH system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Evolution
  • Chromatography, High Pressure Liquid
  • Chromatography, Liquid
  • Crassostrea / embryology*
  • Crassostrea / metabolism*
  • DNA-Binding Proteins / genetics
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation, Developmental
  • Mass Spectrometry
  • Promoter Regions, Genetic / genetics
  • Receptors, Thyroid Hormone / genetics
  • Receptors, Thyroid Hormone / metabolism*
  • Retinoid X Receptors / metabolism
  • Signal Transduction
  • Thyroid Gland / metabolism
  • Thyroxine / metabolism*
  • Transcription, Genetic / drug effects
  • Transcriptional Activation / drug effects
  • Triiodothyronine / analogs & derivatives*
  • Triiodothyronine / metabolism*

Substances

  • DNA-Binding Proteins
  • Receptors, Thyroid Hormone
  • Retinoid X Receptors
  • Triiodothyronine
  • 3,3',5-triiodothyroacetic acid
  • Thyroxine

Grants and funding

This research was financially supported by the National Natural Science Foundation of China (No.31372515 and 31402285), the National Basic Research Program of China (973 Program, 2010CB126401), and the National High Technology Research and Development Program (863 program, 2012AA10A405). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.