TY - JOUR
T1 - Two types of phosphofructokinase-1 differentially regulate the glycolytic pathway in insulin-stimulated chicken skeletal muscle
AU - Seki, Yoshinori
AU - Sato, Kan
AU - Kono, Tatsuyoshi
AU - Akiba, Yukio
N1 - Funding Information:
The authors are grateful for the financial support of the Japan Society for the Promotion of Science. This work was partly supported by Grants-in-Aid (Nos. 13460121 and 15208026) from the Ministry of Education, Science and Culture of Japan. We also acknowledge the excellent technical assistance of H. Matsuyama, M. Ueda, T. Takimoto and A. Aoki.
PY - 2006/3
Y1 - 2006/3
N2 - To elucidate the precise regulation of glucose homeostasis in chicken skeletal muscle, expression of muscle- and liver-type phosphofructokinase-1 (EC:2.7.1.11, PFK-M, PFK-L) was characterized in the insulin-stimulated state by Real-Time PCR. Firstly, chicken PFK-M and PFK-L full-length cDNA sequences were identified. The deduced amino acid sequences were 81.6% and 86.5% identical with human PFK-M and PFK-L, respectively. In pectoralis superficialis (PS) muscle and extensor digitorum longus (EDL), PFK-M mRNA levels were unchanged following insulin stimulation. Surprisingly, although mammalian PFK-L has been reported to be expressed in liver, kidney and brain, chicken PFK-L was not detected in liver and kidney, however, strong expression was detected in skeletal muscle and brain by Northern blot analysis. However, using PCR, PFK-L mRNA was detected in liver. Taken together, chicken PFK-L mRNA expression was at a very low level, below the detection limit of Northern blot analysis. Chicken PFK-L mRNA levels were increased 200% in PS muscle but decreased by 40% in EDL following insulin stimulation. These results suggest that two types of PFK regulate the glycolytic pathway in the insulin-stimulated state and, therefore, that glucose metabolism in chicken skeletal muscle may be regulated in a very different manner compared to mammals.
AB - To elucidate the precise regulation of glucose homeostasis in chicken skeletal muscle, expression of muscle- and liver-type phosphofructokinase-1 (EC:2.7.1.11, PFK-M, PFK-L) was characterized in the insulin-stimulated state by Real-Time PCR. Firstly, chicken PFK-M and PFK-L full-length cDNA sequences were identified. The deduced amino acid sequences were 81.6% and 86.5% identical with human PFK-M and PFK-L, respectively. In pectoralis superficialis (PS) muscle and extensor digitorum longus (EDL), PFK-M mRNA levels were unchanged following insulin stimulation. Surprisingly, although mammalian PFK-L has been reported to be expressed in liver, kidney and brain, chicken PFK-L was not detected in liver and kidney, however, strong expression was detected in skeletal muscle and brain by Northern blot analysis. However, using PCR, PFK-L mRNA was detected in liver. Taken together, chicken PFK-L mRNA expression was at a very low level, below the detection limit of Northern blot analysis. Chicken PFK-L mRNA levels were increased 200% in PS muscle but decreased by 40% in EDL following insulin stimulation. These results suggest that two types of PFK regulate the glycolytic pathway in the insulin-stimulated state and, therefore, that glucose metabolism in chicken skeletal muscle may be regulated in a very different manner compared to mammals.
KW - Chicken
KW - Glucose metabolism
KW - Insulin
KW - Molecular cloning
KW - mRNA expression
KW - Phosphofructokinase-1
KW - Real-Time PCR
KW - Skeletal muscle
UR - http://www.scopus.com/inward/record.url?scp=33344475508&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33344475508&partnerID=8YFLogxK
U2 - 10.1016/j.cbpb.2005.12.006
DO - 10.1016/j.cbpb.2005.12.006
M3 - Article
C2 - 16413217
AN - SCOPUS:33344475508
SN - 1096-4959
VL - 143
SP - 344
EP - 350
JO - Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology
JF - Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology
IS - 3
ER -