Vogel U, Jensen K F
Department of Biological Chemistry, University of Copenhagen, Denmark.
J Bacteriol. 1994 May;176(10):2807-13. doi: 10.1128/jb.176.10.2807-2813.1994.
We determined the rates of mRNA and protein chain elongation on the lacZ gene during exponential growth on different carbon sources. The RNA chain elongation rate was calculated from measurements of the time elapsing between induction of lacZ expression and detection of specific hybridization with a probe near the 3' end of the mRNA. The elongation rate for the transcripts decreased 40% when the growth rate decreased by a factor of 4, and it always correlated with the rate of translation elongation. A similar growth rate dependency was seen for transcription on the infB gene and on a part of the rrnB gene fused to a synthetic, inducible promoter. However, the untranslated RNA chain specified by the rrnB gene was elongated nearly twice as fast as the two mRNA species encoded by infB and lacZ.
我们测定了在不同碳源上指数生长期间,lacZ基因的mRNA和蛋白质链延伸速率。RNA链延伸速率是通过测量从lacZ表达诱导到检测与mRNA 3'端附近探针的特异性杂交之间所经过的时间来计算的。当生长速率降低4倍时,转录本的延伸速率下降了40%,并且它总是与翻译延伸速率相关。对于infB基因以及与合成的可诱导启动子融合的rrnB基因的一部分的转录,也观察到了类似的生长速率依赖性。然而,rrnB基因指定的未翻译RNA链的延伸速度几乎是infB和lacZ编码的两种mRNA的两倍。