PUBLICATION

Partial cloning, tissue distribution and effects of epigallocatechin gallate on hepatic 3-hydroxy-3-methylglutaryl-CoA reductase mRNA transcripts in goldfish (Carassius auratus)

Authors
Cocci, P., Mosconi, G., and Palermo, F.A.
ID
ZDB-PUB-140728-45
Date
2014
Source
Gene   545(2): 220-225 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Catechin/analogs & derivatives*
  • Catechin/pharmacology
  • Cloning, Molecular
  • Gene Expression Regulation/drug effects*
  • Goldfish/classification
  • Goldfish/genetics*
  • Goldfish/metabolism*
  • Hydroxymethylglutaryl CoA Reductases/chemistry
  • Hydroxymethylglutaryl CoA Reductases/genetics*
  • Hydroxymethylglutaryl CoA Reductases/metabolism*
  • Liver/drug effects*
  • Liver/enzymology*
  • Molecular Sequence Data
  • Organ Specificity
  • Phylogeny
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Sequence Alignment
PubMed
24835314 Full text @ Gene
Abstract

Epigallocatechin gallate (EGCG), the major active component of the green tea, has recently been found to inhibit 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCoAR) activity in vitro and to modulate lipogenesis in vivo. In this study we have evaluated the effects of short-term in vivo exposure to EGCG (6 μg g 1 BW or 9 μg g 1 BW) on hepatic HMGCoAR gene expression of goldfish (Carassius auratus). We initially characterized a partial sequence of goldfish HMGCoAR suggesting that the obtained fragment shares high similarity (> 92%) with other fish HMGCoAR sequences. Further, the HMGCoAR transcript was detected in all goldfish tissues (except muscle) but primarily in liver, brain and gonads; on the contrary, low expression levels were found in intestine, heart, gill, and kidney. Both EGCG doses significantly decreased hepatic HMGCoAR mRNA levels 180 min post-injection. HMGCoAR was also significantly down-regulated at 90 min after injection in fish treated with the highest dose of EGCG. Our results demonstrate that hepatic HMGCoAR gene expression is acutely responsive to short-term EGCG exposure in goldfish. This finding suggests a potential role of EGCG in transcriptional regulation of the rate-limiting enzyme in cholesterol synthesis.

Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping