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诱导型一氧化氮合酶(NOS2)启动子CCTTT重复序列多态性:与无症状疟疾流行区人群体内一氧化氮生成/NOS活性的关系

Inducible nitric oxide synthase (NOS2) promoter CCTTT repeat polymorphism: relationship to in vivo nitric oxide production/NOS activity in an asymptomatic malaria-endemic population.

作者信息

Boutlis Craig S, Hobbs Maurine R, Marsh Robyn L, Misukonis Mary A, Tkachuk Ariana N, Lagog Moses, Booth Jennifer, Granger Donald L, Bockarie Moses J, Mgone Charles S, Levesque Marc C, Weinberg J Brice, Anstey Nicholas M

机构信息

International Health Program, Infectious Diseases Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.

出版信息

Am J Trop Med Hyg. 2003 Dec;69(6):569-73.

Abstract

Polymorphisms in the inducible nitric oxide synthase gene (NOS2) promoter have been associated with clinical outcome from malaria. These include a CCTTT repeat (CCTTTn) 2.5 kilobases upstream from the NOS2 transcription start site, and two single nucleotide substitutions: G-->C at position -954 (G-954C), and C-->T at position -1173 (C-1173T). Although hypothesized to influence NO production in vivo, the functional relevance of (CCTTT)n and G-954C is uncertain because disease association studies have yielded inconsistent results. This study found no association between CCTTT repeat number and levels of plasma NO metabolites or peripheral blood mononuclear cell NOS activity in a cohort of asymptomatic malaria-exposed coastal Papua New Guineans 1-60 years old. This suggests that (CCTTT)n does not independently influence NOS2 transcription in vivo. Neither the G-954C nor the C-1173T polymorphisms were identified in this population, indicating the variability and complexity of selection for NOS2 promoter polymorphisms in different malaria-endemic populations.

摘要

诱导型一氧化氮合酶基因(NOS2)启动子的多态性与疟疾的临床结局相关。这些多态性包括位于NOS2转录起始位点上游2.5千碱基处的CCTTT重复序列(CCTTTn),以及两个单核苷酸替换:-954位的G→C(G-954C)和-1173位的C→T(C-1173T)。尽管据推测这些多态性会影响体内一氧化氮的产生,但由于疾病关联研究结果不一致,(CCTTT)n和G-954C的功能相关性仍不确定。本研究在一组年龄为1至60岁、接触过疟疾的无症状沿海巴布亚新几内亚人群中,未发现CCTTT重复序列数量与血浆一氧化氮代谢产物水平或外周血单核细胞NOS活性之间存在关联。这表明(CCTTT)n在体内不会独立影响NOS2转录。该人群中未发现G-954C和C-1173T多态性,这表明不同疟疾流行地区人群中NOS2启动子多态性的选择具有变异性和复杂性。

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