Citation: | QIU Ying, HUANG Guiju, LIU Baosuo, FAN Sigang, LI Youning, CHEN Mingqiang, YU Dahui. Cloning of GLUT1 gene from winged pearl oyster Pteria penguin and its expression in response to glucose challenge[J]. South China Fisheries Science, 2016, 12(5): 81-89. DOI: 10.3969/j.issn.2095-0780.2016.05.010 |
Facilitated glucose transporter type 1 (GLUT1) takes part in transporting glucose in most animal tissues responsible for energy metabolism. To study function of GLUT1 in Pteria penguin, the cDNA sequence of GLUT1 was obtained from P.penguin transcriptome using RACE, which was named as PpGLUT1. The full length cDNA was 2 068 bp, The gene encoded 522 amino acids, 12 transmembrane helical motifs and multiple phosphorylation sites, with N-terminal and C-terminal on the cytoplasmic side.The molecular weight was 57.226 4 kD and the isoelectric point was 5.17. Fluorescent quantitative PCR results show that PpGLUT1 expressed in all tissues and was significantly low in muscle. The high concentration of 0.5 g·mL-1 glucose injection result shows that the expression of PpGLUT1 increased within 30 min after injected, and then decreased; at the injection time of 2 h, the expression of PpGLUT1 was lowest; the expression gradually increased after 2 h. Different concentrations of glucose injection test indicate that the expression levels of PpGLUT1 increased with increase of glucose concentrations ranging from 0.1 g·mL-1 to 0.4 g·mL-1 and then decreased. The mRNA expression responses to glucose suggests that PpGLUT1 plays an important role in glucose transportation in multiple tissues of P.penguin.
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