Dubnau D
EMBO J. 1985 Feb;4(2):533-7. doi: 10.1002/j.1460-2075.1985.tb03661.x.
ermC confers resistance to macrolide-lincosamide streptogramin B antibiotics by specifying a ribosomal RNA methylase, which results in decreased ribosomal affinity for these antibiotics. ermC expression is induced by exposure to erythromycin. We have previously proposed a translational regulation model in which erythromycin causes stalling of a ribosome, which is translating a leader peptide. Stalling causes a conformation shift in the ermC mRNA which in turn unmasks the methylase ribosomal binding site. A prediction of this translational attenuation model for ermC induction was tested by replacing the second codon of the putative ermC leader peptide coding region by TAA. As expected, the introduction of this mutation resulted in an uninducible phenotype which was suppressible by two ochre suppressor mutations in Bacillus subtilis. It is concluded that translation through the leader peptide coding region, in frame with the predicted leader peptide, is required for ermC induction.
ermC 通过产生一种核糖体 RNA 甲基化酶赋予对大环内酯 - 林可酰胺 - 链阳菌素 B 类抗生素的抗性,这导致核糖体对这些抗生素的亲和力降低。ermC 的表达由接触红霉素诱导。我们之前提出了一种翻译调控模型,其中红霉素导致正在翻译前导肽的核糖体停滞。停滞导致 ermC mRNA 的构象发生变化,进而使甲基化酶核糖体结合位点暴露。通过将假定的 ermC 前导肽编码区的第二个密码子替换为 TAA,对这种 ermC 诱导的翻译衰减模型的一个预测进行了测试。正如预期的那样,引入这种突变导致了一种不可诱导的表型,该表型可被枯草芽孢杆菌中的两个赭石抑制突变所抑制。得出的结论是,ermC 诱导需要通过与预测的前导肽读框一致的前导肽编码区进行翻译。