首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Role of Runt-related Transcription Factor 3 (RUNX3) in Transcription Regulation of Natural Cytotoxicity Receptor 1 (NCR1/NKp46) an Activating Natural Killer (NK) Cell Receptor
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Role of Runt-related Transcription Factor 3 (RUNX3) in Transcription Regulation of Natural Cytotoxicity Receptor 1 (NCR1/NKp46) an Activating Natural Killer (NK) Cell Receptor

机译:矮子相关转录因子3(RUNX3)在活化自然杀伤(NK)细胞受体天然细胞毒性受体1(NCR1 / NKp46)的转录调控中的作用

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摘要

Natural cytotoxicity receptor 1 (NCR1), also known as NKp46, is a natural killer (NK) lymphocyte-activating receptor. It is involved in major aspects of NK immune function and shows a high degree of lineage specificity in blood and bone marrow. The nature of its NK-restricted expression is not well understood. In this study, we confirm that human NCR1 NK-specific expression is achieved at the mRNA level. We found two key cis-regulatory elements in the immediate vicinity upstream of the gene. One element acts as an essential promoter, whereas the other acts as a tissue-dependent enhancer/repressor. This latter regulatory element contains a runt related-transcription factor (RUNX) recognition motif that preferentially binds RUNX3. Interfering with RUNX proteins using a dominant negative form results in decreased Ncr1 expression. RUNX3 overexpression had the opposite effect. These findings shed light on the role of RUNX3 in the control of an important NK-activating receptor.
机译:天然细胞毒性受体1(NCR1),也称为NKp46,是天然杀伤(NK)淋巴细胞激活受体。它涉及NK免疫功能的主要方面,并且在血液和骨髓中显示出高度的谱系特异性。 NK限制表达的性质尚未完全了解。在这项研究中,我们确认了在mRNA水平上实现了人类NCR1 NK特异性表达。我们在该基因的上游附近发现了两个关键的顺式调控元件。一个元件充当必需的启动子,而另一个充当组织依赖性增强子/阻遏物。后一个调节元件包含优先结合RUNX3的矮子相关转录因子(RUNX)识别基序。使用显性负向形式干扰RUNX蛋白会导致Ncr1表达降低。 RUNX3过表达具有相反的效果。这些发现揭示了RUNX3在重要的NK激活受体控制中的作用。

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