首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Bovine glucose transporter GLUT8: cloning, expression, and developmental regulation in mammary gland
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Bovine glucose transporter GLUT8: cloning, expression, and developmental regulation in mammary gland

机译:牛葡萄糖转运蛋白GLUT8:乳腺的克隆,表达和发育调控

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摘要

GLUT8 is a newly identified member of the facilitative glucose transporter family, which characteristically exhibits high-affinity glucose transport activity. The expression of GLUT8 has been shown to depend on gonadotropin secretion in human testes and to be regulated by insulin in the blastocyst. To characterize GLUT8 and investigate its role in normal mammary gland function, we cloned and sequenced the full-length cDNA of bovine GLUT8. The 2073-base-pair cDNA sequence is predicted to encode a protein of 478 amino acids, with a molecular weight of approximately 51 kDa. The deduced amino acid sequence of bovine GLUT8 is 90%, 84%, 84% and 58% identical to human, mouse, rat and chicken GLUT8, and is 26%, 27% and 24% identical to bovine GLUT1, GLUT3 and GLUT4, respectively. Bovine GLUT8 retains the characteristic structural features of GLUT8 proteins previously identified from other species including membrane spanning helices, glucose transporter motifs, an N-linked glycosylation site on loop 9 and a putative dileucine internalization motif. The major in vitro transcription and translation product of bovine GLUT8 cDNA migrated at an apparent molecular weight of 38 kDa similar to the sizes reported for GLUT8 from other mammalian species. In the presence of canine microsomal membranes, the translation product increased to 40 kDa suggesting glycosylation. Transient transfection studies using a FLAG epitope tagged construct in COS-7 cells revealed that bovine GLUT8 is localized to the cytoplasm in non-stimulated conditions. A 2.1-kb GLUT8 mRNA transcript was detected at high levels in bovine testes, at moderate levels in lactating bovine mammary gland, lung, kidney, spleen, intestine and skeletal muscle, and at low levels in bovine liver. GLUT8 mRNA expression in bovine mammary gland increased about 10-fold (P<0.001) during late pregnancy and early lactation, similar to the pattern of change in GLUT1 mRNA and more dramatic than the increase seen in mouse mammary gland. These results suggest that GLUT8 expression may be regulated by lactogenic hormones and that GLUT8 may play a role in glucose uptake in the lactating mammary gland. (C) 2004 Elsevier B.V. All rights reserved.
机译:GLUT8是促进性葡萄糖转运蛋白家族的新成员,其特征在于具有高亲和力的葡萄糖转运活性。已经显示GLUT8的表达取决于人睾丸中促性腺激素的分泌,并受胚泡中胰岛素的调节。为了表征GLUT8并研究其在正常乳腺功能中的作用,我们克隆并测序了牛GLUT8的全长cDNA。预测2073个碱基对的cDNA序列编码一个478个氨基酸的蛋白质,分子量约为51 kDa。牛GLUT8的推导氨基酸序列与人,小鼠,大鼠和鸡GLUT8的同源性为90%,84%,84%和58%,与牛GLUT1,GLUT3和GLUT4的同源性为26%,27%和24%,分别。牛GLUT8保留了先前从其他物种鉴定出的GLUT8蛋白的特征性结构特征,包括跨膜螺旋,葡萄糖转运蛋白基序,环9上的N-联糖基化位点和推定的双亮氨酸内化基序。牛GLUT8 cDNA的主要体外转录和翻译产物以38 kDa的表观分子量迁移,与其他哺乳动物物种GLUT8报道的大小相似。在犬微粒体膜的存在下,翻译产物增加至40 kDa,表明糖基化。在COS-7细胞中使用标记有FLAG表位的构建体进行的瞬时转染研究表明,牛GLUT8在非刺激条件下定位于细胞质。在牛睾丸中检测到2.1-kb GLUT8 mRNA转录水平高,在泌乳的牛乳腺,肺,肾,脾,肠和骨骼肌中检测到中等水平,而在牛肝中检测到低水平。牛乳腺中的GLUT8 mRNA表达在怀孕后期和早期哺乳期增加了约10倍(P <0.001),与GLUT1 mRNA的变化模式相似,并且比小鼠乳腺中的变化更显着。这些结果表明,GLUT8的表达可能受泌乳激素的调节,并且GLUT8可能在泌乳的乳腺中吸收葡萄糖。 (C)2004 Elsevier B.V.保留所有权利。

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