Mudd E A, Carpousis A J, Krisch H M
Department of Molecular Biology, University of Geneva, Switzerland.
Genes Dev. 1990 May;4(5):873-81. doi: 10.1101/gad.4.5.873.
Bacteriophage T4 mRNAs are markedly stabilized, both chemically and functionally, in an Escherichia coli strain deficient in the RNA-processing endonuclease RNase E. The functional stability of total T4 messages increased 6-fold; we were unable to detect a T4 message whose functional stability was not increased. There was a 4-fold increase in the chemical stability of total T4 RNA. The degree of chemical stabilization of six specific T4 mRNAs examined varied from a maximum of 28-fold to a minimum of 1.5-fold. In the RNase E-deficient strain, several minutes delay and a slower rate of progeny production led to a reduction in final phage yield of approximately 50%. Although the effect of the rne temperature-sensitive mutation could be indirect, the simplest interpretation of our results is that RNase E acts directly in the degradation of many T4 mRNAs.
在缺乏RNA加工内切核酸酶RNase E的大肠杆菌菌株中,噬菌体T4的mRNA在化学和功能上都得到了显著稳定。总T4信使的功能稳定性提高了6倍;我们无法检测到功能稳定性未增加的T4信使。总T4 RNA的化学稳定性提高了4倍。所检测的六种特定T4 mRNA的化学稳定程度从最大28倍到最小1.5倍不等。在缺乏RNase E的菌株中,几分钟的延迟和较慢的子代产生速率导致最终噬菌体产量降低约50%。尽管rne温度敏感突变的影响可能是间接的,但对我们结果最简单的解释是,RNase E直接作用于许多T4 mRNA的降解。