Rasmussen E B, Lis J T
Section of Biochemistry Molecular and Cell Biology, Cornell University, Ithaca New York, 14853, USA.
J Mol Biol. 1995 Oct 6;252(5):522-35. doi: 10.1006/jmbi.1995.0517.
Expression of the hsp70 gene of Drosophila melanogaster is controlled at the level of transcript elongation. In the uninduced state, hsp70 possesses an RNA polymerase II complex, elongationally engaged, but paused early in the transcription unit. In this study, we have used a powerful new selection-amplification technique to analyze the RNA transcripts associated with such "paused polymerases" under non-heat shock and heat shock-induced conditions. They reveal a region of pausing on the uninduced gene in vivo spanning from +21 to +35. This region is interrupted by an area of low polymerase density, centered at about +26. Upon induction, an accumulation of short transcripts, similar in size to those associated with the paused complex, was seen. Models for polymerase pausing and release are discussed in light of these data. The increased sensitivity of our new technique also allowed us to investigate ternary complexes associated with genes with much lower levels of engaged RNA polymerase. These included two of the small heat shock genes (hsp26 and hsp27) and two metabolic genes (Gapdh-1 and Gapdh-2), where paused polymerases were thought to be present, plus two other genes (Mtn and yp1), where polymerase pausing has not been detected in the past. In both of the small heat shock genes, we found evidence of previously unknown sites of transcriptional termination, residing immediately upstream of the regions of polymerase pausing.
黑腹果蝇hsp70基因的表达在转录延伸水平受到调控。在未诱导状态下,hsp70拥有一个RNA聚合酶II复合物,该复合物处于延伸状态,但在转录单元早期暂停。在本研究中,我们使用了一种强大的新筛选-扩增技术,来分析在非热休克和热休克诱导条件下与这种“暂停的聚合酶”相关的RNA转录本。它们揭示了体内未诱导基因上一个从+21到+35的暂停区域。该区域被一个以大约+26为中心的低聚合酶密度区域中断。诱导后,观察到短转录本的积累,其大小与那些与暂停复合物相关的转录本相似。根据这些数据讨论了聚合酶暂停和释放的模型。我们新技术提高的灵敏度还使我们能够研究与参与的RNA聚合酶水平低得多的基因相关的三元复合物。这些基因包括两个小热休克基因(hsp26和hsp27)和两个代谢基因(Gapdh-1和Gapdh-2),据认为在这些基因中存在暂停的聚合酶,另外还有两个基因(Mtn和yp1),过去在这些基因中未检测到聚合酶暂停。在这两个小热休克基因中,我们发现了以前未知的转录终止位点的证据,这些位点位于聚合酶暂停区域的紧邻上游。