天然细胞毒性受体NKp44基因在人NK细胞白血病中的转录调控

Kenichiro Ito, M. Kawana, T. Iwata, K. Higai
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引用次数: 1

摘要

天然细胞毒性受体NKp44是NK细胞功能的重要调节因子。我们之前报道过NKp44与肝素具有结合亲和力,并且人肝癌HepG2细胞(HepTF)产生的含多聚唾液酸Lewis X的转铁蛋白比其他天然细胞毒性受体表达更高。为了进一步了解天然细胞毒性受体之间的差异,我们试图了解NKp44在KHYG-1人NK白血病细胞中的基因转录调控。cDNA末端的5 '快速扩增揭示了NKp44转录起始位点的位置,从而鉴定了5 '非转录区。双荧光素酶分析结果表明,NKp44基因的表达调控受转录起始位点的-1963 ~ -1599 nt区和-352 ~ -231 nt区影响。-410至+ 1nt区域包含转录因子AP-1、Oct-1、HNF-4和Pax-4的潜在结合位点。这些结果表明,NKp44基因5 '侧的特定区域对NKp44的转录和调控很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptional Regulation of the Natural Cytotoxicity Receptor NKp44 Gene in Human NK Cell Leukemia
The natural cytotoxicity receptor NKp44 is an important regulator of NK cell function. We have previously reported that NKp44 has binding affinity to heparin and the transferrin containing multimeric sialyl Lewis X produced by human hepatoma HepG2 cells (HepTF) is more highly expressed than the other natural cytotoxicity receptors. To further understand the differences between natural cytotoxicity receptors, we sought to understand the gene transcriptional regulation of NKp44 in KHYG-1 human NK leukemia cells. 5′-rapid amplification of cDNA ends revealed the location of the NKp44 transcription initiation sites allowing identification of the 5′ untranscribed region. The result of the dual luciferase assay suggested that regulation of NKp44 gene expression is affected by the -1963 to -1599 nt region and the -352 to -231 nt region relative to the transcription initiation sites. The -410 to +1 nt region contained potential binding sites for the transcription factors AP-1, Oct-1, HNF-4, and Pax-4. These results suggest that defined regions in the 5′-flanking region of NKp44 gene is important for NKp44 transcription and regulation.
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