Jan J, Valle F, Bolivar F, Merino E
Departamento de Microbiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Mexico.
FEMS Microbiol Lett. 2000 Feb 1;183(1):9-14. doi: 10.1111/j.1574-6968.2000.tb08926.x.
The aprE gene of Bacillus subtilis encodes the major serine alkaline protease known as subtilisin. It is expressed during the transition state and transcribed by the sigma(A) form of the RNA polymerase (RNAP). In this work, we characterized the regulatory region of the aprE gene (rraprE) from B. subtilis. By computer analysis and site-directed mutagenesis, we localized the aprE promoter sequence 7 bp upstream from its transcription initiation site (TIS). We also characterized the static curvature properties of the rraprE DNA and found two different areas of DNA bending, within the first 400 bp upstream of its TIS. We postulate that these particular curved DNA regions could play a role in the interaction with some regulatory proteins and discuss possible implications related to aprE transcription regulation.
枯草芽孢杆菌的aprE基因编码主要的丝氨酸碱性蛋白酶,即枯草杆菌蛋白酶。它在过渡态表达,并由RNA聚合酶(RNAP)的σ(A)形式转录。在这项工作中,我们对枯草芽孢杆菌aprE基因的调控区域(rraprE)进行了表征。通过计算机分析和定点诱变,我们将aprE启动子序列定位在其转录起始位点(TIS)上游7 bp处。我们还对rraprE DNA的静态曲率特性进行了表征,发现在其TIS上游前400 bp内有两个不同的DNA弯曲区域。我们推测这些特定的弯曲DNA区域可能在与某些调控蛋白的相互作用中发挥作用,并讨论了与aprE转录调控相关的可能影响。