Thyroperoxidase
Thyroid Hormones

Author: Gianpiero Pescarmona
Date: 06/01/2012

Description

DEFINITION

A short protein description with the molecular wheight, isoforms, etc...
Use, when available, the link to Wikipedia (Es Trypsin)

External links not available on Wikipedia have to be added here

THE GENE

DatabaseLink
WikigenesACADM
GeneCards"URL":
Your Favorite Gene Sigma"URL":

Wikigenes includes links to

  • NCBI Gene
  • NCBI SNP
  • iHOP resource
  • OMIM
  • SNPedia
  • UniProt
  • Ensembl
  • HGNC

CHEMICAL STRUCTURE AND IMAGES

When relevant for the function

  • Primary structure
  • Secondary structure
  • Tertiary structure
  • Quaternary structure


Protein Aminoacids Percentage
The Protein Aminoacids Percentage gives useful information on the local environment and the metabolic status of the cell (starvation, lack of essential AA, hypoxia)

Protein Aminoacids Percentage (Width 700 px)

SYNTHESIS AND TURNOVER

mRNA synthesis
protein synthesis

post-translational modifications
degradation

CELLULAR FUNCTIONS

cellular localization,
biological function

  • Enzymes
DatabaseLink
BRENDA - The Comprehensive Enzyme Information System"URL":
KEGG Pathways"URL":
Human Metabolome Database"URL":
  • Cell signaling and Ligand transport
  • Structural proteins

REGULATION

Thyroperoxidase NIS

Inducers

Thyroperoxidase mRNA in quiescent and proliferating thyroid epithelial cells: expression and subcellular localization studied by in situ hybridization. 1993

Using in situ hybridization procedure, we have investigated the regulation and the cellular localization of thyroperoxidase (TPO) messenger RNA accumulation as a marker of differentiation in dog thyroid epithelial cells in primary culture. The response to different mitogens (TSH acting through cAMP, EGF and TPA) has been compared. TPO mRNA accumulation was exquisitely dependent on a continuous TSH/cAMP stimulation. It was induced within 1 h in the whole cell population from a very low basal level. This effect was inhibited by the cAMP-independent mitogens EGF and TPA. By contrast, the TSH-induction of TPO mRNA accumulation was observed irrespectively of the proliferative activity of the cells, i.e. in the presence or the absence of insulin, which is required for mitogenesis. The short half-life of TPO mRNA (+/- 2 h) implies that it was continuously transcribed during TSH/cAMP-dependent cell cycling. As compared to another thyroid differentiation marker, thyroglobulin mRNA (Pohl et al., J. Cell Biol. 111, 663-672 (1990)), TPO mRNA accumulation differed by the rapidity of its control by cAMP, the pattern of its intercellular heterogeneity, and the unexpected segregation to a perinuclear region, probably the nuclear envelope that constitutes a specialized part of the endoplasmic reticulum. Despite these differences, both TPO and thyroglobulin gene transcriptions are unequivocally compatible with the cell cycle when induced by cAMP, at variance with the generally observed antagonism between growth and differentiation expression.

Repressors

Moderate doses of iodide in vivo inhibit cell proliferation and the expression of thyroperoxidase and Na+/I- symporter mRNAs in dog thyroid. 1997

Thyroglobulin regulates follicular function and heterogeneity by suppressing thyroid-specific gene expression. 1999

BRAF mutations in papillary thyroid carcinomas inhibit genes involved in iodine metabolism. 2007
Quantitative PCR was used to measure mRNA levels for the sodium/iodide symporter (NIS), apical iodide transporter (AIT-B), thyroglobulin (Tg), thyroperoxidase (TPO), TSH receptor (TSH-R), the transcription factor PAX8, and glucose transporter type 1 (Glut1).

Retinoic acid modulation of thyroid dual oxidase activity in rats and its impact on thyroid iodine organification. 2010
In this group, NIS function and TPO activity were unchanged, whereas DuOx activity was significantly decreased, which might have contributed to the decrease in iodine organification.

DIAGNOSTIC USE

AddThis Social Bookmark Button