Altman Sidney, Wesolowski Donna, Guerrier-Takada Cecilia, Li Yong
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06520, USA.
Proc Natl Acad Sci U S A. 2005 Aug 9;102(32):11284-9. doi: 10.1073/pnas.0505271102. Epub 2005 Aug 1.
RNase P from Escherichia coli cleaves the coenzyme B12 riboswitch from E. coli and a similar one from Bacillus subtilis. The cleavage sites do not occur in any recognizable structure, as judged from theoretical schemes that have been drawn for these 5' UTRs. However, it is possible to draw a scheme that is a good representation of the E. coli cleavage site for RNase P and for the cleavage site in B. subtilis. These data indicate that transient structures are important in RNase P cleavage and in riboswitch function. Coenzyme B12 has a small inhibitory effect on E. coli RNase P cleavage of the E. coli riboswitch. Both E. coli RNase P and a partially purified RNase P from Aspergillus nidulans mycelia succeeded in cleaving a putative arginine riboswitch from A. nidulans. The cleavage site may be a representative of another model substrate for eukaryotic RNase P. This 5' UTR controls splicing of the arginase mRNA in A. nidulans. Four other riboswitches in E. coli were not cleaved by RNase P under the conditions tested.
来自大肠杆菌的核糖核酸酶P可切割大肠杆菌的辅酶B12核糖开关以及枯草芽孢杆菌的类似核糖开关。根据为这些5'非翻译区绘制的理论示意图判断,切割位点并不出现在任何可识别的结构中。然而,有可能绘制出一个能很好地呈现大肠杆菌核糖核酸酶P的切割位点以及枯草芽孢杆菌中切割位点的示意图。这些数据表明,瞬时结构在核糖核酸酶P切割和核糖开关功能中很重要。辅酶B12对大肠杆菌核糖核酸酶P切割大肠杆菌核糖开关有轻微抑制作用。大肠杆菌核糖核酸酶P和来自构巢曲霉菌丝体的部分纯化核糖核酸酶P都成功切割了构巢曲霉的一个假定精氨酸核糖开关。该切割位点可能是真核核糖核酸酶P另一种模型底物的代表。这个5'非翻译区控制着构巢曲霉中精氨酸酶mRNA的剪接。在所测试的条件下,大肠杆菌中的其他四个核糖开关未被核糖核酸酶P切割。