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猿猴空泡病毒40增强子可被切割成多个片段,每个片段都具有不同的细胞类型特异性。

The SV40 enhancer can be dissected into multiple segments, each with a different cell type specificity.

作者信息

Schirm S, Jiricny J, Schaffner W

机构信息

Institute für Molekularbiologie II der Universität Zürich, Switzerland.

出版信息

Genes Dev. 1987 Mar;1(1):65-74. doi: 10.1101/gad.1.1.65.

Abstract

The SV40 enhancer is known to be active in a wide variety of tissues and species. It contains a number of sequence motifs that can be bound by protein factors and whose integrity is essential for full enhancer activity. We have individually analyzed three synthetic oligonucleotides derived from sequences present within the SV40 enhancer: two oligonucleotides contain variants of the enhancer "core" sequence (designated corePVUII and coreC) and the third represents a region containing a decanucleotide homology to the immunoglobulin promoters/enhancers (designated SPHI). The oligonucleotides were multimerized and linked to a beta-globin test gene. Transcripts of the test gene were analyzed following transient expression in 10 cell lines representing a broad spectrum of tissues. We show that each of the three short segments can individually act as an enhancer when present in multiple copies. None of these enhancers is ubiquitously active; however, each shows activity in a distinctive subpopulation of cell lines. This cell type specificity is most remarkable in the case of the two oligonucleotide segments containing the core sequences. One of these is primarily active in CV-1 cells, whereas the other exhibits a cell type specificity identical to that of the entire enhancer, possibly identifying it as the most important sequence element within the native SV40 enhancer. Our data suggest that a particular cell type specificity is typical for individual enhancer segments, and that enhancers of differing specificity can be assembled from the individual sequence motifs by combining them in different patterns.

摘要

已知SV40增强子在多种组织和物种中具有活性。它包含一些可被蛋白质因子结合的序列基序,其完整性对于增强子的完全活性至关重要。我们分别分析了源自SV40增强子内序列的三种合成寡核苷酸:两种寡核苷酸包含增强子“核心”序列的变体(分别命名为corePVUII和coreC),第三种代表与免疫球蛋白启动子/增强子具有十核苷酸同源性的区域(命名为SPHI)。将这些寡核苷酸多聚化并连接到β-珠蛋白测试基因上。在代表广泛组织类型的10种细胞系中进行瞬时表达后,分析测试基因的转录本。我们发现,当以多拷贝形式存在时,这三个短片段中的每一个都可以单独作为增强子发挥作用。这些增强子均无普遍活性;然而,每个增强子在不同的细胞系亚群中都表现出活性。这种细胞类型特异性在包含核心序列的两个寡核苷酸片段的情况下最为显著。其中一个主要在CV-1细胞中具有活性,而另一个则表现出与整个增强子相同的细胞类型特异性,这可能表明它是天然SV40增强子中最重要的序列元件。我们的数据表明,特定的细胞类型特异性是单个增强子片段的典型特征,并且不同特异性的增强子可以通过以不同模式组合各个序列基序来组装而成。

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