PUBLICATION

Dietary iron alters waterborne-copper induced gene expression in softwater acclimated zebrafish (Danio rerio)

Authors
Craig, P.M., Galus, M., Wood, C.M., and McClelland, G.B.
ID
ZDB-PUB-081110-7
Date
2009
Source
American journal of physiology. Regulatory, integrative and comparative physiology   296(2): R362-R373 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Acclimatization*
  • Adenosine Triphosphatases/metabolism
  • Animals
  • Body Weight
  • Cation Transport Proteins/metabolism
  • Copper Radioisotopes
  • Copper Sulfate/toxicity*
  • Female
  • Gastrointestinal Tract/drug effects
  • Gastrointestinal Tract/metabolism
  • Gene Expression Regulation/drug effects
  • Gills/drug effects
  • Gills/metabolism
  • Iron, Dietary/metabolism
  • Iron, Dietary/toxicity*
  • Liver/drug effects
  • Liver/metabolism
  • Male
  • Membrane Transport Proteins/genetics
  • Membrane Transport Proteins/metabolism*
  • Metallothionein/metabolism
  • Transcription, Genetic/drug effects
  • Water Pollutants, Chemical/toxicity*
  • Zebrafish/genetics
  • Zebrafish/metabolism*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
PubMed
18987288 Full text @ Am. J. Physiol. Regul. Integr. Comp. Physiol.
CTD
18987288
Abstract
Metals like iron (Fe) and copper (Cu) function as integral components in many biological reactions and in excess, these essential metals are toxic, and organisms must control metal acquisition and excretion. We examined the effects of chronic waterborne Cu exposure and the interactive effects of elevated dietary Fe on gene expression and tissue metal accumulation in zebrafish. Softwater acclimated zebrafish exposed to 8microg/L Cu, with and without supplementation of a diet high in Fe (560 vs 140 mg Fe/kg food) for 21d demonstrated a significant reduction in liver and gut Cu load relative to waterborne Cu exposure alone. Gene expression levels for divalent metal transport (DMT)-1, copper transporter (CTR)-1 and the basolateral metal transporter ATP7A in the gills and gut increased when compared to controls, but the various combinations of Cu and high Fe diet revealed altered levels of expression. Further examination of the basolateral Fe transporter, ferroportin, showed responses to waterborne Cu exposure in the gut, and a significant increase with Fe treatment alone in the liver. Additionally, we examined metallothionein 1 & 2 (MT1 & MT2), which indicated that MT2 is more responsive to Cu load. To explore the relationship between transcription and protein function, we examined both CTR-1 protein levels and gill apical uptake of radiolabelled Cu(64), which demonstrated decreased Cu uptake and protein abundance in the elevated Cu treatments. This study shows that high dietary Fe can significantly alter the genetic expression pattern of Cu transporters at the level of the gill, liver, and gastrointestinal tract. Key words: Zebrafish, Copper, Gene expression, CTR-1.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping