Dundr M, Raska I
Institute of Experimental Medicine, Academy of Sciences of Czech Republic, Prague.
Exp Cell Res. 1993 Sep;208(1):275-81. doi: 10.1006/excr.1993.1247.
A nonradioactive ultrastructural method based on the incorporation of 5-bromouridine-5'-triphosphate into the RNA of streptolysin O-permeabilized cultured HeLa cells is described and used for the visualization of rRNA transcription sites. Even though the method provides much better resolution than ultrastructural autoradiography, the results obtained do not allow the assignment of rRNA transcription to a single nucleolar structural component. We locate the rRNA transcription sites at the border region of fibrillar centers with dense fibrillar components. In addition, the method represents a convenient tool for the in situ immunodetection of extranucleolar RNA synthesis.
描述了一种基于将5-溴尿苷-5'-三磷酸掺入经链球菌溶血素O通透处理的培养HeLa细胞RNA中的非放射性超微结构方法,并将其用于可视化rRNA转录位点。尽管该方法提供的分辨率比超微结构放射自显影好得多,但获得的结果不允许将rRNA转录定位到单个核仁结构成分。我们将rRNA转录位点定位在纤维中心与致密纤维成分的边界区域。此外,该方法是用于核仁外RNA合成原位免疫检测的便捷工具。