Marvaud J C, Gibert M, Inoue K, Fujinaga Y, Oguma K, Popoff M R
Unité des Toxines Microbiennes, Institut Pasteur, Paris, France.
Mol Microbiol. 1998 Aug;29(4):1009-18. doi: 10.1046/j.1365-2958.1998.00985.x.
The genes of the botulinum neurotoxin A (BoNT) complex are clustered in a locus consisting of two divergent polycistronic operons, one containing the non-toxic, non-haemagglutinin (NTNH) component and bontA genes, the other containing the haemagglutinin (HA) component genes. The two operons are separated by a gene (botR/A, previously called orf21) encoding a 21 kDa protein. A recombinant Clostridium botulinum A strain that overexpresses botR/A was constructed by electroporating strain 62 with the vector pAT19 containing botR/A under the control of its own promoter. The transformed strain produced more BoNT/A and associated non-toxic proteins (ANTPs) and the corresponding mRNAs than the non-transformed strain. Partial inhibition of botR/A by antisense mRNA resulted in lower levels of BoNT/A, NTNH and HA70 and the levels of the corresponding mRNAs. Gel mobility shift assays and immunoprecipitations showed that BotR/A bound to the DNA promoter region upstream from the two BoNT/A complex operons. These results show that botR/A activated transcription of the genes encoding BoNT/A and ANTPs in C. botulinum A by interacting directly with the region promoter, and that the homologous genes in C. botulinum B, C and D presumably have the same function.
肉毒杆菌神经毒素A(BoNT)复合体的基因聚集在一个位点,该位点由两个反向多顺反子操纵子组成,一个包含无毒、无血凝素(NTNH)成分和bontA基因,另一个包含血凝素(HA)成分基因。这两个操纵子被一个编码21 kDa蛋白质的基因(botR/A,以前称为orf21)隔开。通过用含有在其自身启动子控制下的botR/A的载体pAT19对62株进行电穿孔,构建了一种过表达botR/A的重组肉毒杆菌A菌株。与未转化菌株相比,转化菌株产生了更多的BoNT/A和相关无毒蛋白(ANTPs)以及相应的mRNA。反义mRNA对botR/A的部分抑制导致BoNT/A、NTNH和HA70水平降低以及相应mRNA水平降低。凝胶迁移率变动分析和免疫沉淀表明,BotR/A与两个BoNT/A复合体操纵子上游的DNA启动子区域结合。这些结果表明,botR/A通过直接与区域启动子相互作用激活了肉毒杆菌A中编码BoNT/A和ANTPs的基因的转录,并且肉毒杆菌B、C和D中的同源基因可能具有相同的功能。