Santos J M, Drider D, Marujo P E, Lopez P, Arraiano C M
Instituto de Tecnologia Quimica e Biológica, Universidade Nova de Lisboa, Oeiras, Portugal.
FEMS Microbiol Lett. 1997 Dec 1;157(1):31-8. doi: 10.1111/j.1574-6968.1997.tb12749.x.
A comparative analysis of mRNA decay was carried out in Escherichia coli using the wild-type and an isogenic RNase III deletion strain. We have studied the mRNA degradation from the Escherichia coli gene bolA, the Lactococcus lactis biovar diacetylactis citQRP operon and the Desulfovibrio vulgaris Hildenborough gene cyc. As seen by a dramatic stabilization of the specific mRNAs in the mutant strain, RNase III was crucial for the decay process of these three messages. Since RNase III, unlike RNase E, is not essential for bacterial viability we think that there is potential for using RNase III mutant strains to modulate gene expression.
利用野生型和同基因RNase III缺失菌株在大肠杆菌中进行了mRNA衰变的比较分析。我们研究了大肠杆菌bolA基因、乳酸乳球菌双乙酰亚种citQRP操纵子和脱硫弧菌希登伯勒菌株cyc基因的mRNA降解情况。正如在突变菌株中特定mRNA显著稳定所显示的那样,RNase III对这三种信使的衰变过程至关重要。由于与RNase E不同,RNase III对细菌生存力并非必不可少,我们认为利用RNase III突变菌株调节基因表达具有潜力。