Uchida I, Makino S, Sekizaki T, Terakado N
National Institute of Animal Health, Ibaraki, Japan.
Mol Microbiol. 1997 Mar;23(6):1229-40. doi: 10.1046/j.1365-2958.1997.3041667.x.
The two major virulence factors of Bacillus anthracis are the tripartite toxin and the polyglutamate capsule, which are encoded by genes on the large plasmids, pXO1 and pXO2, respectively. The genes atxA, located on pXO1, and acpA, located on pXO2, encode positive trans-acting proteins that are involved in bicarbonate-mediated regulation of toxin and capsule production, respectively. A derivative strain cured of pXO1 produced less capsular substance than the parent strain harbouring both pXO1 and pXO2, and electroporation of the strain cured of pXO1 with a plasmid containing the cloned atxA gene resulted in an increased level of capsule production. An acpA-null mutant was complemented by not only acpA but also the atxA gene. The cap region, which is essential for encapsulation, contains three genes capB, capC, and capA, arranged in that order. The atxA gene stimulated capsule synthesis from the cloned cap region. Transcriptional analysis of cap by RNA slot-blot hybridization and primer-extension analysis revealed that atxA activated expression of cap in trans at the transcriptional level. These results indicate that cross-talk occurs, in which the pXO1-located gene, atxA, activates transcription of the cap region genes located on pXO2. We identified two major apparent transcriptional start sites, designated P1 and P2, located at positions 731 bp and 625 bp, respectively, upstream of the translation-initiation codon of capB. Transcription initiated from P1 and P2 was activated by both atxA and acpA, and activation appeared to be stimulated by bicarbonate. Deletion analysis of the upstream region of the cap promoter revealed that activation by both atxA and acpA required a DNA segment of 70 bp extending upstream of the P1 site. These results suggest that cross-talk by atxA to the genes encoding capsule synthesis is caused by the interaction of the atxA gene product with a regulatory sequence upstream of cap.
炭疽芽孢杆菌的两个主要毒力因子是三联毒素和聚谷氨酸荚膜,它们分别由大质粒pXO1和pXO2上的基因编码。位于pXO1上的atxA基因和位于pXO2上的acpA基因分别编码正向反式作用蛋白,它们分别参与碳酸氢盐介导的毒素和荚膜产生的调控。缺失pXO1的衍生菌株产生的荚膜物质比同时含有pXO1和pXO2的亲本菌株少,用含有克隆的atxA基因的质粒对缺失pXO1的菌株进行电穿孔导致荚膜产生水平增加。一个acpA缺失突变体不仅被acpA而且被atxA基因互补。对于荚膜形成必不可少的cap区域包含按此顺序排列的三个基因capB、capC和capA。atxA基因刺激了来自克隆的cap区域的荚膜合成。通过RNA斑点杂交和引物延伸分析对cap进行转录分析表明,atxA在转录水平上反式激活cap的表达。这些结果表明存在串扰,其中位于pXO1上的基因atxA激活位于pXO2上的cap区域基因的转录。我们确定了两个主要的明显转录起始位点,分别命名为P1和P2,位于capB翻译起始密码子上游731 bp和625 bp处。从P1和P2起始的转录被atxA和acpA激活,并且激活似乎受到碳酸氢盐的刺激。对cap启动子上游区域的缺失分析表明,atxA和acpA的激活都需要一个延伸到P1位点上游70 bp的DNA片段。这些结果表明,atxA对编码荚膜合成的基因的串扰是由atxA基因产物与cap上游的调控序列相互作用引起的。