Zhang Yonglong, Zhang Junjie, Hoeflich Klaus P, Ikura Mitsuhiko, Qing Guoliang, Inouye Masayori
Department of Biochemistry, Robert Wood Johnson Medical School, 675 Hoes Lane, Piscataway, NJ 08854, USA.
Mol Cell. 2003 Oct;12(4):913-23. doi: 10.1016/s1097-2765(03)00402-7.
Escherichia coli contains operons called "addiction modules," encoding toxin and antitoxin, which are responsible for growth arrest and cell death. Here, we demonstrate that MazF toxin encoded by "mazEF addiction module" is a sequence-specific (ACA) endoribonuclease functional only for single-stranded RNA. MazF works as a ribonuclease independent of ribosomes, and is, therefore, functionally distinct from RelE, another E. coli toxin, which assists mRNA cleavage at the A site on ribosomes. Upon induction, MazF cleaves whole cellular mRNAs to efficiently block protein synthesis. Purified MazF inhibited protein synthesis in both prokaryotic and eukaryotic cell-free systems. This inhibition was released by MazE, the labile antitoxin against MazF. Thus, MazF functions as a toxic endoribonuclease to interfere with the function of cellular mRNAs by cleaving them at specific sequences leading to rapid cell growth arrest and cell death. The role of such endoribonucleases may have broad implication in cell physiology under various growth conditions.
大肠杆菌含有被称为“成瘾模块”的操纵子,其编码毒素和抗毒素,这些负责生长停滞和细胞死亡。在此,我们证明由“mazEF成瘾模块”编码的MazF毒素是一种仅对单链RNA起作用的序列特异性(ACA)核糖核酸内切酶。MazF作为一种独立于核糖体的核糖核酸酶发挥作用,因此,在功能上不同于另一种大肠杆菌毒素RelE,RelE协助在核糖体上的A位点切割mRNA。诱导后,MazF切割整个细胞的mRNA以有效阻断蛋白质合成。纯化的MazF在原核和真核无细胞系统中均抑制蛋白质合成。这种抑制作用可被MazE释放,MazE是针对MazF的不稳定抗毒素。因此,MazF作为一种有毒的核糖核酸内切酶,通过在特定序列处切割细胞mRNA来干扰其功能,导致细胞快速生长停滞和细胞死亡。这种核糖核酸内切酶的作用可能在各种生长条件下的细胞生理学中具有广泛的意义。