Ramamoorthy R, Schmidt F J
Department of Biochemistry, University of Missouri, Columbia 65212.
FEBS Lett. 1991 Dec 16;295(1-3):227-9. doi: 10.1016/0014-5793(91)81424-7.
Strong pauses at nucleotides +118 and +121 relative to the transcriptional start occur during in vitro transcription of the E. coli rnpB gene encoding the catalytic M1 RNA subunit of Ribonuclease P. These pauses are immediately downstream of 2 phylogenetically conserved stem-loop structures in the RNA. In the present work, single-base changes which disrupted Watson-Crick base-pairing in the hairpins were introduced into rnpB. Transcription studies in vitro with these modified templates revealed that none of the nucleotide changes predicted to increase or decrease the stability of the first hairpin significantly affected the pause half-lives. A mutation which disrupted the second hairpin increased the pause half-life 2-fold. The data suggest that the upstream stem and loop structures in the transcript are not involved in the pausing event.
在体外转录编码核糖核酸酶P催化性M1 RNA亚基的大肠杆菌rnpB基因过程中,相对于转录起始点,在核苷酸+118和+121处出现强烈停顿。这些停顿位于RNA中两个系统发育保守的茎环结构的紧邻下游。在本研究中,将破坏发夹结构中沃森-克里克碱基配对的单碱基变化引入rnpB。用这些修饰模板进行的体外转录研究表明,预测会增加或降低第一个发夹稳定性的核苷酸变化均未显著影响停顿半衰期。破坏第二个发夹的突变使停顿半衰期增加了2倍。数据表明转录本中的上游茎环结构不参与停顿事件。