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Genetic Control of Variegated KIR Gene Expression: Polymorphisms of the Bi-Directional KIR3DL1 Promoter Are Associated with Distinct Frequencies of Gene Expression

机译:杂色KIR基因表达的遗传控制:双向KIR3DL1启动子的多态性与基因表达的不同频率相关

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Natural killer (NK) cells play an important role in the detection and elimination of tumors and virus-infected cells by the innate immune system. Human NK cells use cell surface receptors (KIR) for class I MHC to sense alterations of class I on potential target cells. Individual NK cells only express a subset of the available KIR genes, generating specialized NK cells that can specifically detect alteration of a particular class I molecule or group of molecules. The probabilistic behavior of human KIR bi-directional promoters is proposed to control the frequency of expression of these variegated genes. Analysis of a panel of donors has revealed the presence of several functionally relevant promoter polymorphisms clustered mainly in the inhibitory KIR family members, especially the KIR3DL1 alleles. We demonstrate for the first time that promoter polymorphisms affecting the strength of competing sense and antisense promoters largely explain the differential frequency of expression of KIR3DL1 allotypes on NK cells. KIR3DL1/S1 subtypes have distinct biological activity and coding region variants of the KIR3DL1/S1 gene strongly influence pathogenesis of HIV/AIDS and other human diseases. We propose that the polymorphisms shown in this study to regulate the frequency of KIR3DL1/S1 subtype expression on NK cells contribute substantially to the phenotypic variation across allotypes with respect to disease resistance.
机译:天然杀伤(NK)细胞在通过先天免疫系统检测和消除肿瘤和病毒感染的细胞中起着重要作用。人类NK细胞使用I类MHC的细胞表面受体(KIR)来感知潜在靶细胞上I类的改变。单个NK细胞仅表达可用KIR基因的子集,从而生成可以特异性检测特定I类分子或分子组改变的专门化NK细胞。人类KIR双向启动子的概率行为被提议来控制这些杂色基因的表达频率。对一组供体的分析显示,存在几种功能相关的启动子多态性,这些启动子多态性主要集中在抑制性KIR家族成员中,尤其是KIR3DL1等位基因。我们第一次证明启动子多态性影响竞争有义和反义启动子的强度很大程度上解释了NK细胞上KIR3DL1同种异型表达的差异频率。 KIR3DL1 / S1亚型具有独特的生物学活性,KIR3DL1 / S1基因的编码区变体强烈影响HIV / AIDS和其他人类疾病的发病机理。我们建议本研究中所示的多态性,以调节NK细胞上KIR3DL1 / S1亚型的表达频率,在很大程度上改变了同种异型在抗病性方面的表型变异。

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