Glycogen synthase 2 is a novel target gene of peroxisome proliferator-activated receptors
Glycogen synthase 2 (Gys-2) is the ratelimiting enzyme in the storage of glycogen in liver and adipose tissue, yet little is known about regulation of Gys-2 transcription. The peroxisome proliferator-activated receptors (PPARs) are transcription factors involved in the regulation of lipid and glucose metabolism and might be hypothesized to govern glycogen synthesis as well. Here, we show that Gys-2 is a direct target gene of PPAR¿, PPARß/¿ and PPAR¿. Expression of Gys-2 is significantly reduced in adipose tissue of PPAR¿¿/¿, PPARß/¿¿/¿ and PPAR¿+/¿ mice. Furthermore, synthetic PPARß/¿, and ¿ agonists markedly up-regulate Gys-2 mRNA and protein expression in mouse 3T3-L1 adipocytes. In liver, PPAR¿ deletion leads to decreased glycogen levels in the refed state, which is paralleled by decreased expression of Gys-2 in fasted and refed state. Two putative PPAR response elements (PPREs) were identified in the mouse Gys-2 gene: one in the upstream promoter (DR-1prom) and one in intron 1 (DR-1int). It is shown that DR-1int is the response element for PPARs, while DR-1prom is the response element for Hepatic Nuclear Factor 4 alpha (HNF4¿). In adipose tissue, which does not express HNF4¿, DR-1prom is occupied by PPARß/¿ and PPAR¿, yet binding does not translate into transcriptional activation of Gys-2. Overall, we conclude that mouse Gys-2 is a novel PPAR target gene and that transactivation by PPARs and HNF4¿ is mediated by two distinct response elements.
| Main Authors: | , , , , , , , , , |
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| Format: | Article/Letter to editor biblioteca |
| Language: | English |
| Subjects: | adipose-tissue, alpha ppar-alpha, beta/delta, fatty-acid oxidation, gamma, glycogen-synthase, in-vivo, metabolism, response elements, skeletal-muscle, |
| Online Access: | https://research.wur.nl/en/publications/glycogen-synthase-2-is-a-novel-target-gene-of-peroxisome-prolifer |
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| Summary: | Glycogen synthase 2 (Gys-2) is the ratelimiting enzyme in the storage of glycogen in liver and adipose tissue, yet little is known about regulation of Gys-2 transcription. The peroxisome proliferator-activated receptors (PPARs) are transcription factors involved in the regulation of lipid and glucose metabolism and might be hypothesized to govern glycogen synthesis as well. Here, we show that Gys-2 is a direct target gene of PPAR¿, PPARß/¿ and PPAR¿. Expression of Gys-2 is significantly reduced in adipose tissue of PPAR¿¿/¿, PPARß/¿¿/¿ and PPAR¿+/¿ mice. Furthermore, synthetic PPARß/¿, and ¿ agonists markedly up-regulate Gys-2 mRNA and protein expression in mouse 3T3-L1 adipocytes. In liver, PPAR¿ deletion leads to decreased glycogen levels in the refed state, which is paralleled by decreased expression of Gys-2 in fasted and refed state. Two putative PPAR response elements (PPREs) were identified in the mouse Gys-2 gene: one in the upstream promoter (DR-1prom) and one in intron 1 (DR-1int). It is shown that DR-1int is the response element for PPARs, while DR-1prom is the response element for Hepatic Nuclear Factor 4 alpha (HNF4¿). In adipose tissue, which does not express HNF4¿, DR-1prom is occupied by PPARß/¿ and PPAR¿, yet binding does not translate into transcriptional activation of Gys-2. Overall, we conclude that mouse Gys-2 is a novel PPAR target gene and that transactivation by PPARs and HNF4¿ is mediated by two distinct response elements. |
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