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人类嗜T淋巴细胞病毒I型(HTLV-I)启动子活性的比较分析显示不存在与疾病相关的表达模式。

Comparative analysis of HTLV-I promoter activities reveals no disease-linked pattern of expression.

作者信息

Gonzalez-Dunia D, Komurian-Pradel F, Chirinian-Syan S, De The G, Brahic M, Ozden S

机构信息

Département des Rétrovirus, UA Centre National de Recherche Scientifique (CNRS) 1157, Institut Pasteur, Paris, France.

出版信息

AIDS Res Hum Retroviruses. 1993 Apr;9(4):337-41. doi: 10.1089/aid.1993.9.337.

Abstract

To investigate the possibility of an association between the type of pathology caused by HTLV-I and the activity of its promoter, we compared the levels of transcription obtained with six LTRs isolated from patients with two different HTLV-I-related diseases: ATL and TSP/HAM. The patients came from different geographical endemic areas. The LTR region was amplified by polymerase chain reaction (PCR) from the DNA of uncultured peripheral blood lymphocytes, and directly cloned upstream of the luciferase reporter gene. Constructs were tested by a transient transfection assay in a variety of cell lines. Although the activities of these LTRs were statistically different in some of the cell lines tested, no correlation could be demonstrated between the promoter activity and the nature of the disease. Thus, the data suggest that the LTR is not a major determinant of the nature of the disease associated with the infection by HTLV-I.

摘要

为了研究人类嗜T淋巴细胞病毒I型(HTLV-I)所致病理类型与其启动子活性之间存在关联的可能性,我们比较了从患有两种不同HTLV-I相关疾病(成人T细胞白血病/淋巴瘤(ATL)和热带痉挛性截瘫/HTLV-I相关脊髓病(TSP/HAM))的患者中分离出的六个长末端重复序列(LTR)的转录水平。这些患者来自不同的地理流行区。通过聚合酶链反应(PCR)从未培养的外周血淋巴细胞DNA中扩增LTR区域,并直接克隆到荧光素酶报告基因的上游。通过瞬时转染试验在多种细胞系中对构建体进行检测。尽管在一些测试的细胞系中这些LTR的活性存在统计学差异,但启动子活性与疾病性质之间未显示出相关性。因此,数据表明LTR不是与HTLV-I感染相关疾病性质的主要决定因素。

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