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Published on: January 14, 2013
Expression analysis of glycerol synthesis-related liver transcripts in rainbow smelt (Osmerus mordax) exposed to a
Jennifer R Hall1, Connie E Short, Matthew L Rise
1Ocean Sciences Centre, Memorial University of Newfoundland, St. John's, Newfoundland A1C 5S7, Canada. jrhall@mun.ca
Physiological and Biochemical Zoology : PBZ
|January 13, 2012
Summary
Rainbow smelt increase glycerol to survive cold by breaking down glycogen and inhibiting pyruvate oxidation. This metabolic shift channels energy towards glycerol production, preventing freezing.
Area of Science:
- * Biochemistry and molecular biology
- * Environmental physiology
- * Aquatic animal adaptation
Background:
- * Rainbow smelt (Osmerus mordax) accumulate glycerol to prevent freezing in subzero temperatures.
- * Glyceroneogenesis, a metabolic pathway, is activated by cold and occurs in the liver, branching from glycolysis and gluconeogenesis.
Purpose of the Study:
- * To investigate the metabolic and transcriptomic changes in rainbow smelt during a cold acclimation.
- * To identify genes and pathways involved in glycerol production in response to decreasing temperatures.
Main Methods:
- * Controlled temperature transition from 8°C to 0°C for rainbow smelt.
- * Measurement of carbohydrate and liver transcript levels of 21 genes.
- * Comparison of gene expression and metabolite levels between warm (8°C) and cold (0°C) acclimated smelt.
Main Results:
- * Cold smelt showed lower liver glycogen and higher phosphoglucomutase transcript levels compared to warm smelt.
- * Plasma glycerol levels increased over time in cold smelt, with elevated phosphofructokinase and pyruvate dehydrogenase kinase transcript levels.
- * Increased plasma glucose, liver glucose-6-phosphatase, and lipoprotein lipase transcript levels were observed in cold smelt.
Conclusions:
- * Glycerol production in rainbow smelt is fueled by glycogen degradation.
- * Inhibition of pyruvate oxidation directs metabolic flux towards glycerol synthesis.
- * Upregulation of lipoprotein lipase suggests enhanced lipid breakdown, and glutamine synthetase may aid nitrogen storage for future biosynthesis.

