Friedrich-Schiller-Universität Jena, Biologisch-Pharmazeutische Fakultät, AG Bakteriengenetik, Philosophenweg 12, Jena, Germany.
Mol Microbiol. 2012 Feb;83(3):579-98. doi: 10.1111/j.1365-2958.2011.07952.x. Epub 2012 Jan 9.
Here, we describe bsrG/SR4, a novel type I toxin-antitoxin system from the SPβ prophage region of the Bacillus subtilis chromosome. The 294-nucleotide bsrG RNA encodes a 38-amino-acid toxin, whereas SR4 is a 180-nucleotide antisense RNA that acts as the antitoxin. Both genes overlap by 123 nucleotides. BsrG expression increases at the onset of stationary phase. The sr4 promoter is 6- to 10-fold stronger than the bsrG promoter. Deletion of sr4 stabilizes bsrG mRNA and causes cell lysis on agar plates, which is due to the BsrG peptide and not the bsrG mRNA. SR4 overexpression could compensate cell lysis caused by overexpression of bsrG. SR4 interacts with the 3' UTR of bsrG RNA, thereby promoting its degradation. RNase III cleaves the bsrG RNA/SR4 duplex at position 185 of bsrG RNA, but is not essential for the function of the toxin-antitoxin system. Endoribonuclease Y and 3'-5' exoribonuclease R participate in the degradation of both bsrG RNA and SR4, whereas PnpA processes three SR4 precursors to the mature RNA. A heat shock at 48°C results in faster degradation and, therefore, significantly decreased amounts of bsrG RNA.
在这里,我们描述了来自枯草芽孢杆菌染色体 SPβ 噬菌体区域的新型 I 型毒素-抗毒素系统 bsrG/SR4。294 个核苷酸的 bsrG RNA 编码一个 38 个氨基酸的毒素,而 SR4 是一个 180 个核苷酸的反义 RNA,作为抗毒素。两个基因重叠 123 个核苷酸。bsrG 的表达在停滞期开始时增加。sr4 启动子比 bsrG 启动子强 6-10 倍。sr4 的缺失稳定了 bsrG mRNA,并导致琼脂平板上的细胞裂解,这是由于 BsrG 肽而不是 bsrG mRNA。SR4 的过表达可以补偿 bsrG 过表达引起的细胞裂解。SR4 与 bsrG RNA 的 3'UTR 相互作用,从而促进其降解。RNase III 在 bsrG RNA 的位置 185 处切割 bsrG RNA/SR4 双链体,但对毒素-抗毒素系统的功能不是必需的。内切核酸酶 Y 和 3'-5'外切核酸酶 R 参与 bsrG RNA 和 SR4 的降解,而 PnpA 将三个 SR4 前体加工成成熟 RNA。在 48°C 的热激导致更快的降解,因此 bsrG RNA 的含量显著降低。