Krishnan S N, Haddad G G
Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut 06520-8064, USA.
Life Sci. 1995;56(14):1193-7. doi: 10.1016/0024-3205(95)00058-e.
Using PCR, glucose transporter-3 (GLUT3) was cloned in its entirety from rat brain. The similarity between human, murine and rodent glucose transporter-3 proteins exceeds 90%. Such extensive sequence conservation suggests that essentially all regions of the protein, including the transmembrane domains, are functionally important. This clone can be used to study GLUT3 expression in the rat by Northern analysis or in situ hybridization, or the sequence can be used to generate peptide antibodies. Finally, the availability of a probe for glucose transporter-3 in the rat allows studies of the regulation of GLUT3 gene expression in neurons under a variety of physiological and pathophysiological conditions.
利用聚合酶链反应(PCR),从大鼠脑中完整克隆了葡萄糖转运蛋白3(GLUT3)。人、小鼠和啮齿动物的葡萄糖转运蛋白3蛋白质之间的相似性超过90%。如此广泛的序列保守性表明该蛋白质的几乎所有区域,包括跨膜结构域,在功能上都很重要。该克隆可用于通过Northern分析或原位杂交研究大鼠体内GLUT3的表达,或者该序列可用于生成肽抗体。最后,大鼠葡萄糖转运蛋白3探针的可得性使得在各种生理和病理生理条件下研究神经元中GLUT3基因表达的调控成为可能。