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免疫球蛋白启动子可独立于增强子展现细胞类型特异性。

An immunoglobulin promoter displays cell-type specificity independently of the enhancer.

作者信息

Foster J, Stafford J, Queen C

出版信息

Nature. 1985;315(6018):423-5. doi: 10.1038/315423a0.

Abstract

Recent studies in which cloned immunoglobulin genes were introduced into cultured cells have produced two significant findings. First, the genes are expressed after transfection into lymphoid cells but not non-lymphoid cells. Second, transcription of an immunoglobulin gene requires, in addition to the promoter region, an enhancer element located downstream of the transcription start site. These findings raise the question of whether it is the promoter or the enhancer region that is responsible for the observed cell-type specificity. It has, in fact, been shown that immunoglobulin enhancers function only in lymphoid cells. We show here that the promoter for an immunoglobulin kappa light-chain gene also is strongly specific for lymphoid cells. Our result reemphasizes the importance of promoters relative to enhancers in determining which cells express which genes.

摘要

最近将克隆的免疫球蛋白基因导入培养细胞的研究产生了两个重要发现。第一,这些基因转染到淋巴细胞后能表达,但转染到非淋巴细胞后则不能表达。第二,免疫球蛋白基因的转录除了需要启动子区域外,还需要一个位于转录起始位点下游的增强子元件。这些发现提出了一个问题,即究竟是启动子还是增强子区域导致了所观察到的细胞类型特异性。事实上,已经表明免疫球蛋白增强子仅在淋巴细胞中起作用。我们在此表明,免疫球蛋白κ轻链基因的启动子对淋巴细胞也具有很强的特异性。我们的结果再次强调了启动子相对于增强子在决定哪些细胞表达哪些基因方面的重要性。

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