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首页> 外文期刊>Molecules and cells >Regulatory elements involved in transcription of the human NeuAc alpha 2,3Gal beta 1,3GaINAc alpha 2,6-sialyltransferase (hST6GaINAc IV) gene
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Regulatory elements involved in transcription of the human NeuAc alpha 2,3Gal beta 1,3GaINAc alpha 2,6-sialyltransferase (hST6GaINAc IV) gene

机译:调控元件参与人类NeuAc alpha 2,3Gal beta 1,3GaINAc alpha 2,6-唾液酸转移酶(hST6GaINAc IV)基因的转录

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摘要

We previously cloned and characterized the promoter region of the human NeuAcalpha2,3Galbeta1,3GalNAcalpha2,6sialyltransferase (hST6GalNAc IV) gene [Kim et at. (2003)]. In the present study, we identified a region of 294 bp upstream of exon 1 of the gene that produced maximal transcriptional activity in human Jurkat T cells. Site-directed mutagenesis and transient transfection assays demonstrated that Sp1 and MZF1 elements in this region were required for the promoter activity. Further analysis by electrophoretic mobility shift assays using specific competitors and antibody revealed that Sp1 and MZF1 nuclear proteins interacted with these elements. These results indicate that Sp1 and MZF1 are involved in the transcriptional regulation of the hST6GalNAc IV gene in Jurkat T cells.
机译:我们先前克隆并鉴定了人类NeuAcalpha2,3Galbeta1,3GalNAcalpha2,6唾液酸转移酶(hST6GalNAc IV)基因的启动子区域[Kim等。 (2003)]。在本研究中,我们确定了在人类Jurkat T细胞中产生最大转录活性的基因外显子1上游294 bp的区域。定点诱变和瞬时转染实验表明,该区域的Sp1和MZF1元件是启动子活性所必需的。使用特定的竞争者和抗体通过电泳迁移率变动分析进行的进一步分析显示,Sp1和MZF1核蛋白与这些元素相互作用。这些结果表明Sp1和MZF1参与Jurkat T细胞中hST6GalNAc IV基因的转录调控。

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