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利用原子力显微镜以单分子分辨率成像RNA聚合酶-釉原蛋白基因复合体。

Imaging RNA polymerase-amelogenin gene complexes with single molecule resolution using atomic force microscopy.

作者信息

Crampton Neal, Thomson Neil H, Kirkham Jennifer, Gibson Carolyn W, Bonass William A

机构信息

School of Physics and Astronomy, University of Leeds, and Department of Oral Biology, Leeds Dental Institute, UK.

出版信息

Eur J Oral Sci. 2006 May;114 Suppl 1:133-8; discussion 164-5, 380-1. doi: 10.1111/j.1600-0722.2006.00274.x.

Abstract

The AMELX gene encoding the enamel matrix protein, amelogenin, is located within (and in the opposite orientation to) the first intron of the ARHGAP6 gene, which encodes a GTPase-activating protein. The orientation of these two genes with respect to each other raises the possibility that they may undergo simultaneous convergent transcription during amelogenesis. The aim of this study was to use atomic force microscopy (AFM) to study a transcriptionally active amelogenin DNA template and to investigate the binding of RNA polymerase to convergently aligned promoters. Images of RNA polymerases stalled on DNA templates were obtained following incubation of the template with RNA polymerases and ribonucleotide triphosphates. A linear DNA template incorporating an intact rat amelogenin cDNA flanked by convergently aligned coliphage T7 and T3 promoters was constructed and shown to be transcriptionally active in vitro. Atomic force microscopy images of transcription complexes revealed globular structures, corresponding to single RNA polymerase molecules bound at specific locations on the DNA templates. These results indicate that AFM allows the visualization of individual RNA polymerases on DNA templates, offering a realistic approach to investigating the concept of convergent transcription of nested genes, which may lead to an understanding of whether the simultaneous expression of AMELX and ARHGAP6 is possible during the formation of tooth enamel.

摘要

编码釉基质蛋白釉原蛋白的AMELX基因位于ARHGAP6基因的第一个内含子内(且方向相反),ARHGAP6基因编码一种GTP酶激活蛋白。这两个基因彼此的方向增加了它们在釉质形成过程中可能同时进行汇聚转录的可能性。本研究的目的是使用原子力显微镜(AFM)研究转录活性的釉原蛋白DNA模板,并研究RNA聚合酶与汇聚排列的启动子的结合。在模板与RNA聚合酶和三磷酸核糖核苷酸孵育后,获得了停滞在DNA模板上的RNA聚合酶的图像。构建了一个线性DNA模板,其包含完整的大鼠釉原蛋白cDNA,两侧是汇聚排列的噬菌体T7和T3启动子,并证明其在体外具有转录活性。转录复合物的原子力显微镜图像显示出球状结构,对应于结合在DNA模板特定位置的单个RNA聚合酶分子。这些结果表明,AFM能够可视化DNA模板上的单个RNA聚合酶,为研究嵌套基因的汇聚转录概念提供了一种切实可行的方法,这可能有助于理解在牙釉质形成过程中AMELX和ARHGAP6是否可能同时表达。

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