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抗终止子BoxA对大肠杆菌转录延伸动力学及ppGpp抑制转录延伸的影响

Effects of the antiterminator BoxA on transcription elongation kinetics and ppGpp inhibition of transcription elongation in Escherichia coli.

作者信息

Vogel U, Jensen K F

机构信息

Department of Biological Chemistry, University of Copenhagen, Denmark.

出版信息

J Biol Chem. 1995 Aug 4;270(31):18335-40. doi: 10.1074/jbc.270.31.18335.

DOI:10.1074/jbc.270.31.18335
PMID:7629155
Abstract

It has been shown previously that two different mRNA chains (lacZ and infB) are elongated at a rate of approximately 40 nucleotides (nt)/s during steady state growth on minimal medium and that the rate of mRNA chain elongation is inhibited by ppGpp in vivo. On the other hand, it was found that a truncated ribosomal RNA chain was elongated at a rate of approximately 80 nt/s, independent of growth condition (Vogel, U., and Jensen, K. F. (1994) J. Biol. Chem. 269, 16236-16241). We reasoned that the different transcriptional behavior of mRNA genes and rRNA operons might be caused by the antiterminator sequences present in the rRNA operons. To test this possibility, we have (a) inserted the minimal antiterminator boxA sequence between the promoter and the lacZ and infB genes and (b) deleted the antiterminator sequences from the rRNA transcription unit and measured transcription elongation rates in vivo on the resulting hybrid genes. We found that insertion of boxA in front of the coding region of lacZ increased the transcription elongation rate from 42 nt/s to 69 nt/s during steady state growth and that it eliminated the ppGpp-dependent decrease in the transcription elongation rate during the stringent response. On the other hand, deletion of the antiterminator sequences from the rRNA operon resulted in a reduced transcription elongation rate, but the elongation rate was still insensitive to changes in the ppGpp pool. These results are consistent with the hypothesis that the antiterminator boxA is a primary determinant of the rate of transcription elongation rate.

摘要

先前的研究表明,在基本培养基上稳态生长期间,两条不同的mRNA链(lacZ和infB)以约40个核苷酸(nt)/秒的速率延伸,并且mRNA链延伸速率在体内受到ppGpp的抑制。另一方面,发现一条截短的核糖体RNA链以约80 nt/秒的速率延伸,与生长条件无关(Vogel,U.和Jensen,K.F.(1994)J. Biol. Chem. 269,16236 - 16241)。我们推测,mRNA基因和rRNA操纵子不同的转录行为可能是由rRNA操纵子中存在的抗终止子序列引起的。为了验证这种可能性,我们进行了以下操作:(a)在启动子与lacZ和infB基因之间插入最小抗终止子boxA序列;(b)从rRNA转录单元中删除抗终止子序列,并在体内测量所得杂交基因的转录延伸速率。我们发现,在稳态生长期间,在lacZ编码区前插入boxA可使转录延伸速率从42 nt/秒提高到69 nt/秒,并且消除了严格反应期间ppGpp依赖的转录延伸速率降低。另一方面,从rRNA操纵子中删除抗终止子序列导致转录延伸速率降低,但延伸速率对ppGpp库的变化仍然不敏感。这些结果与抗终止子boxA是转录延伸速率的主要决定因素这一假设一致。

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