Knecht D, Kern H, Scherczinger C
Department of Molecular and Cell Biology, University of Connecticut, Storrs 06269.
Biochim Biophys Acta. 1993 Oct 19;1216(1):105-9. doi: 10.1016/0167-4781(93)90042-c.
Numerous transformation vectors for Dictyostelium discoideum have been constructed by fusing actin 6 and 15 promoters to selectable markers such as G418 and hygromycin. Strand specific probing of RNAs from transformed cells demonstrates that cells containing these vectors accumulate transcripts representing both strands of the vector. The evidence is consistent with bidirectional transcription initiating in the truncated actin promoter fragments. A larger fragment of the actin 15 promoter largely eliminates this problem.
通过将肌动蛋白6和15启动子与诸如G418和潮霉素等选择标记融合,构建了许多用于盘基网柄菌的转化载体。对来自转化细胞的RNA进行链特异性探测表明,含有这些载体的细胞积累了代表载体两条链的转录本。证据表明,双向转录起始于截短的肌动蛋白启动子片段。肌动蛋白15启动子的一个更大片段在很大程度上消除了这个问题。