Clarke Emily, Rahman Nusrat, Page Natalie, Rolph Michael S, Stewart Graeme J, Jones Graham J
Institute for Immunology and Allergy Research, Westmead Millennium Institute, University of Sydney, Westmead, Australia.
J Allergy Clin Immunol. 2008 May;121(5):1148-1154.e3. doi: 10.1016/j.jaci.2008.02.028. Epub 2008 Apr 11.
Polymorphisms in the plant homeodomain finger protein 11 gene (PHF11) are associated with increased total serum IgE levels, asthma, and severe atopic dermatitis (AD) in children. Although PHF11 includes a plant homeodomain, a motif often found in transcriptional regulators, the function of PHF11 has not been investigated.
We sought to test (1) whether PHF11 regulates the transcription of genes involved in allergic disorders and (2) whether polymorphisms in PHF11 predict changes in the expression or function of this gene.
Microarray analysis was used to examine the expression of PHF11 in different immune cell subsets, and the function of PHF11 was tested by using small interfering RNA-induced knockdown or overexpression of PHF11 in primary CD4+ T cells or Jurkat T cells. Genotype-dependent effects on PHF11 expression were tested by using an allele-specific gene expression, and the transcriptional activity of PHF11 was determined by using luciferase hybrid gene reporter assays and in vitro DNA-binding electromobility shift assays.
PHF11 expression was higher in T(H)1 cells relative to that in T(H)2 cells, and knockdown of PHF11 expression reduced expression of the T(H)1-type cytokines IFN-gamma and IL-2. The G-allele of a 3' untranslated region polymorphism associated with AD was correlated with reduced abundance of PHF11 RNA in T(H)1 cells, as well as an increase in a PHF11 isoform lacking exon II. Evidence was also found for a physical and functional interaction between PHF11 and the p65 subunit of nuclear factor kappaB.
PHF11 is a regulator of T(H)1-type cytokine gene expression. The reduction in PHF11 expression seen with an AD-associated genotype could contribute to the strong T(H)2 responses that characterize many allergic individuals.
植物同源异型结构域指蛋白11基因(PHF11)的多态性与儿童血清总IgE水平升高、哮喘及重度特应性皮炎(AD)相关。尽管PHF11包含一个植物同源异型结构域,这是一种在转录调节因子中常发现的基序,但PHF11的功能尚未得到研究。
我们试图测试(1)PHF11是否调节参与过敏性疾病的基因转录,以及(2)PHF11中的多态性是否可预测该基因表达或功能的变化。
采用微阵列分析检测PHF11在不同免疫细胞亚群中的表达,并通过在原代CD4+T细胞或Jurkat T细胞中使用小干扰RNA诱导的PHF11敲低或过表达来测试PHF11的功能。通过等位基因特异性基因表达测试基因型对PHF11表达的影响,并使用荧光素酶杂交基因报告分析和体外DNA结合电泳迁移率变动分析来确定PHF11的转录活性。
相对于T(H)2细胞,PHF11在T(H)1细胞中的表达更高,敲低PHF11表达会降低T(H)1型细胞因子IFN-γ和IL-2的表达。与AD相关的3'非翻译区多态性的G等位基因与T(H)1细胞中PHF11 RNA丰度降低以及缺乏外显子II的PHF11异构体增加相关。还发现了PHF11与核因子κB的p65亚基之间存在物理和功能相互作用的证据。
PHF11是T(H)1型细胞因子基因表达的调节因子。与AD相关的基因型导致的PHF11表达降低可能促成了许多过敏个体特有的强烈T(H)2反应。