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本文引用的文献

1
NLRC5 negatively regulates the NF-kappaB and type I interferon signaling pathways.NLRC5 负调控 NF-κB 和 I 型干扰素信号通路。
Cell. 2010 Apr 30;141(3):483-96. doi: 10.1016/j.cell.2010.03.040.
2
The nucleotide-binding oligomerization domain-like receptor NLRC5 is involved in IFN-dependent antiviral immune responses.核苷酸结合寡聚化结构域样受体 NLRC5 参与 IFN 依赖性抗病毒免疫反应。
J Immunol. 2010 Feb 15;184(4):1990-2000. doi: 10.4049/jimmunol.0900557. Epub 2010 Jan 8.
3
An epigenetic switch involving NF-kappaB, Lin28, Let-7 MicroRNA, and IL6 links inflammation to cell transformation.一种涉及核因子-κB、Lin28、Let-7微小RNA和白细胞介素6的表观遗传开关将炎症与细胞转化联系起来。
Cell. 2009 Nov 13;139(4):693-706. doi: 10.1016/j.cell.2009.10.014. Epub 2009 Oct 29.
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Nod2 is required for the regulation of commensal microbiota in the intestine.Nod2是调节肠道共生微生物群所必需的。
Proc Natl Acad Sci U S A. 2009 Sep 15;106(37):15813-8. doi: 10.1073/pnas.0907722106. Epub 2009 Sep 1.
5
Regulation of MHC class I assembly and peptide binding.MHC I类分子组装与肽结合的调控
Annu Rev Cell Dev Biol. 2008;24:343-68. doi: 10.1146/annurev.cellbio.24.110707.175347.
6
NLRs at the intersection of cell death and immunity.位于细胞死亡与免疫交叉点的NLRs。
Nat Rev Immunol. 2008 May;8(5):372-9. doi: 10.1038/nri2296.
7
NLR proteins: integral members of innate immunity and mediators of inflammatory diseases.NLR蛋白:先天免疫的重要成员及炎症性疾病的介质
J Leukoc Biol. 2008 Jan;83(1):13-30. doi: 10.1189/jlb.0607402. Epub 2007 Sep 17.
8
GTP-dependent recruitment of CIITA to the class II major histocompatibility complex promoter.GTP依赖的CIITA募集至II类主要组织相容性复合体启动子
J Biol Chem. 2007 Sep 7;282(36):26178-84. doi: 10.1074/jbc.M611747200. Epub 2007 Jul 10.
9
Classical nuclear localization signals: definition, function, and interaction with importin alpha.经典核定位信号:定义、功能及其与输入蛋白α的相互作用。
J Biol Chem. 2007 Feb 23;282(8):5101-5. doi: 10.1074/jbc.R600026200. Epub 2006 Dec 14.
10
All the peptides that fit: the beginning, the middle, and the end of the MHC class I antigen-processing pathway.所有适配的肽段:MHC I类抗原加工途径的起始、中间和末端。
Immunol Rev. 2005 Oct;207:31-41. doi: 10.1111/j.0105-2896.2005.00321.x.

NLR 家族成员 NLRC5 是 MHC Ⅰ类基因的转录调节因子。

NLR family member NLRC5 is a transcriptional regulator of MHC class I genes.

机构信息

Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Aug 3;107(31):13794-9. doi: 10.1073/pnas.1008684107. Epub 2010 Jul 16.

DOI:10.1073/pnas.1008684107
PMID:20639463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2922274/
Abstract

MHC class I plays a critical role in the immune defense against viruses and tumors by presenting antigens to CD8 T cells. An NLR protein, class II transactivator (CIITA), is a key regulator of MHC class II gene expression that associates and cooperates with transcription factors in the MHC class II promoter. Although CIITA also transactivates MHC class I gene promoters, loss of CIITA in humans and mice results in the severe reduction of only MHC class II expression, suggesting that additional mechanisms regulate the expression of MHC class I. Here, we identify another member of the NLR protein family, NLRC5, as a transcriptional regulator of MHC class I genes. Similar to CIITA, NLRC5 is an IFN-gamma-inducible nuclear protein, and the expression of NLRC5 resulted in enhanced MHC class I expression in lymphoid as well as epithelial cell lines. Using chromatin immunoprecipitation and reporter gene assays, we show that NLRC5 associates with and activates the promoters of MHC class I genes. Furthermore, we show that the IFN-gamma-induced up-regulation of MHC class I requires NLRC5, because knockdown of NLRC5 specifically impaired the expression of MHC class I. In addition to MHC class I genes, NLRC5 also induced the expression of beta2-microglobulin, transporter associated with antigen processing, and large multifunctional protease, which are essential for MHC class I antigen presentation. Our results suggest that NLRC5 is a transcriptional regulator, orchestrating the concerted expression of critical components in the MHC class I pathway.

摘要

MHC I 类分子在免疫防御病毒和肿瘤中起着至关重要的作用,它将抗原呈递给 CD8 T 细胞。NLR 蛋白,II 类转激活子(CIITA),是 MHC II 类基因表达的关键调节因子,它与 MHC II 启动子中的转录因子结合并合作。尽管 CIITA 也能转激活 MHC I 类基因启动子,但人类和小鼠中 CIITA 的缺失只会导致 MHC II 类表达的严重减少,这表明还有其他机制调节 MHC I 类的表达。在这里,我们发现 NLR 蛋白家族的另一个成员 NLRC5 是 MHC I 类基因的转录调节因子。与 CIITA 相似,NLRC5 是一种 IFN-γ诱导的核蛋白,NLRC5 的表达导致淋巴样和上皮细胞系中 MHC I 类表达增强。通过染色质免疫沉淀和报告基因分析,我们表明 NLRC5 与 MHC I 类基因的启动子结合并激活它们。此外,我们表明 IFN-γ诱导的 MHC I 类上调需要 NLRC5,因为 NLRC5 的敲低特异性地损害了 MHC I 类的表达。除了 MHC I 类基因,NLRC5 还诱导了β2-微球蛋白、抗原加工相关转运体和多功能蛋白酶的表达,这些是 MHC I 类抗原呈递所必需的。我们的结果表明,NLRC5 是一种转录调节因子,协调 MHC I 途径中关键成分的协同表达。