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本文引用的文献

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Polymorphisms of DNA repair and oxidative stress genes in B-cell lymphoma patients.B细胞淋巴瘤患者DNA修复与氧化应激基因的多态性
Biomed Rep. 2013 Jan;1(1):151-155. doi: 10.3892/br.2012.31. Epub 2012 Oct 25.
2
Epigenetic silencing of the human NOS2 gene: rethinking the role of nitric oxide in human macrophage inflammatory responses.人类 NOS2 基因的表观遗传沉默:重新思考一氧化氮在人类巨噬细胞炎症反应中的作用。
J Immunol. 2014 Mar 1;192(5):2326-38. doi: 10.4049/jimmunol.1301758. Epub 2014 Jan 29.
3
Regulation of NO synthesis, local inflammation, and innate immunity to pathogens by BET family proteins.BET 家族蛋白对 NO 合成、局部炎症和病原体固有免疫的调节。
Mol Cell Biol. 2014 Feb;34(3):415-27. doi: 10.1128/MCB.01353-13. Epub 2013 Nov 18.
4
Nitric oxide synthase gene polymorphisms in functional dyspepsia.功能性消化不良中一氧化氮合酶基因多态性。
Dig Dis Sci. 2014 Jan;59(1):72-7. doi: 10.1007/s10620-013-2886-4. Epub 2013 Oct 11.
5
Genetic variation in NOS2A is associated with a sustained virological response to peginterferon plus ribavirin therapy for chronic hepatitis C in Taiwanese Chinese.台湾汉族人群中 NOS2A 的遗传变异与聚乙二醇干扰素联合利巴韦林治疗慢性丙型肝炎的持续病毒学应答相关。
J Med Virol. 2013 Jul;85(7):1206-14. doi: 10.1002/jmv.23598.
6
KLF6 and iNOS regulates apoptosis during respiratory syncytial virus infection.KLF6 和 iNOS 调节呼吸道合胞病毒感染期间的细胞凋亡。
Cell Immunol. 2013 May-Jun;283(1-2):1-7. doi: 10.1016/j.cellimm.2013.06.002. Epub 2013 Jun 18.
7
Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis.一氧化氮合酶:NOS1、NOS2A和NOS3基因与多发性硬化症的关联分析
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8
Expression levels of 10 candidate genes in lung tissue of vaccinated and TB-infected cynomolgus macaques.接种疫苗和感染结核的食蟹猕猴肺组织中10个候选基因的表达水平。
J Med Primatol. 2013 Jun;42(3):161-4. doi: 10.1111/jmp.12040.
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Induction and stability of human Th17 cells require endogenous NOS2 and cGMP-dependent NO signaling.诱导和稳定人 Th17 细胞需要内源性 NOS2 和 cGMP 依赖的 NO 信号。
J Exp Med. 2013 Jul 1;210(7):1433-445. doi: 10.1084/jem.20121277.
10
Loss of methylation in CpG sites in the NF-κB enhancer elements of inducible nitric oxide synthase is responsible for gene induction in human articular chondrocytes.诱导型一氧化氮合酶的核因子κB增强子元件中CpG位点的甲基化缺失是人类关节软骨细胞中基因诱导的原因。
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非人灵长类动物中诱导型一氧化氮合酶(iNOS)调控区变异

Inducible nitric oxide synthase (iNOS) regulatory region variation in non-human primates.

作者信息

Roodgar Morteza, Ross Cody T, Kenyon Nicholas J, Marcelino Gretchen, Smith David Glenn

机构信息

Graduate Group of Comparative Pathology, School of Veterinary Medicine, University of California, Davis, United States; Molecular Anthropology Laboratory, Department of Anthropology, University of California, Davis, United States; California National Primate Research Center (CNPRC), University of California, Davis, United States.

Molecular Anthropology Laboratory, Department of Anthropology, University of California, Davis, United States; Santa Fe Institute, Santa Fe, NM, United States.

出版信息

Infect Genet Evol. 2015 Apr;31:236-44. doi: 10.1016/j.meegid.2015.01.015. Epub 2015 Feb 9.

DOI:10.1016/j.meegid.2015.01.015
PMID:25675838
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4361290/
Abstract

Inducible nitric oxide synthase (iNOS) is an enzyme that plays a key role in intracellular immune response against respiratory infections. Since various species of nonhuman primates exhibit different levels of susceptibility to infectious respiratory diseases, and since variation in regulatory regions of genes is thought to play a key role in expression levels of genes, two candidate regulatory regions of iNOS were mapped, sequenced, and compared across five species of nonhuman primates: African green monkeys (Chlorocebus sabaeus), pig-tailed macaques (Macaca nemestrina), cynomolgus macaques (Macaca fascicularis), Indian rhesus macaques (Macaca mulatta), and Chinese rhesus macaques (M. mulatta). In addition, we conducted an in silico analysis of the transcription factor binding sites associated with genetic variation in these two candidate regulatory regions across species. We found that only one of the two candidate regions showed strong evidence of involvement in iNOS regulation. Specifically, we found evidence of 13 conserved binding site candidates linked to iNOS regulation: AP-1, C/EBPB, CREB, GATA-1, GATA-3, NF-AT, NF-AT5, NF-κB, KLF4, Oct-1, PEA3, SMAD3, and TCF11. Additionally, we found evidence of interspecies variation in binding sites for several regulatory elements linked to iNOS (GATA-3, GATA-4, KLF6, SRF, STAT-1, STAT-3, OLF-1 and HIF-1) across species, especially in African green monkeys relative to other species. Given the key role of iNOS in respiratory immune response, the findings of this study might help guide the direction of future studies aimed to uncover the molecular mechanisms underlying the increased susceptibility of African green monkeys to several viral and bacterial respiratory infections.

摘要

诱导型一氧化氮合酶(iNOS)是一种在针对呼吸道感染的细胞内免疫反应中起关键作用的酶。由于各种非人类灵长类动物对传染性呼吸道疾病表现出不同程度的易感性,并且由于基因调控区域的变异被认为在基因表达水平中起关键作用,因此对iNOS的两个候选调控区域进行了定位、测序,并在五种非人类灵长类动物中进行了比较:非洲绿猴(Chlorocebus sabaeus)、猪尾猕猴(Macaca nemestrina)、食蟹猕猴(Macaca fascicularis)、印度恒河猴(Macaca mulatta)和中国恒河猴(M. mulatta)。此外,我们对这两个候选调控区域跨物种的遗传变异相关的转录因子结合位点进行了计算机分析。我们发现,两个候选区域中只有一个显示出参与iNOS调控的有力证据。具体而言,我们发现了13个与iNOS调控相关的保守结合位点候选证据:AP-1、C/EBPB、CREB、GATA-1、GATA-3、NF-AT、NF-AT5、NF-κB、KLF4、Oct-1、PEA3、SMAD3和TCF11。此外,我们发现跨物种与iNOS相关的几个调控元件(GATA-3、GATA-4、KLF6、SRF、STAT-1、STAT-3、OLF-1和HIF-1)的结合位点存在种间变异证据,特别是相对于其他物种,非洲绿猴的变异尤为明显。鉴于iNOS在呼吸道免疫反应中的关键作用,本研究的结果可能有助于指导未来旨在揭示非洲绿猴对几种病毒和细菌呼吸道感染易感性增加背后分子机制的研究方向。