Anderson D M, Schneewind O
Department of Microbiology and Immunology, Molecular Biology Institute, University of California, Los Angeles, School of Medicine, 10833 Le Conte Avenue, Los Angeles, CA 90095, USA.
Science. 1997 Nov 7;278(5340):1140-3. doi: 10.1126/science.278.5340.1140.
Pathogenic Yersinia species have a specialized secretion system (type III) to target cytotoxic Yop proteins during infection. The signals of YopE and YopN sufficient for the secretion of translational reporter fusions were mapped to the first 15 codons. No common amino acid or peptide sequence could be identified among the secretion signals. Systematic mutagenesis of the secretion signal yielded mutants defective in Yop translation; however, no point mutants could be identified that specifically abolished secretion. Frameshift mutations that completely altered the peptide sequences of these signals also failed to prevent secretion. Thus, the signal that leads to the type III secretion of Yop proteins appears to be encoded in their messenger RNA rather than the peptide sequence.
致病性耶尔森氏菌属物种在感染过程中有一个专门的分泌系统(III型)来靶向细胞毒性Yop蛋白。足以分泌翻译报告融合体的YopE和YopN信号被定位到前15个密码子。在分泌信号中无法鉴定出共同的氨基酸或肽序列。对分泌信号进行系统诱变产生了Yop翻译有缺陷的突变体;然而,未能鉴定出特异性消除分泌的点突变体。完全改变这些信号肽序列的移码突变也未能阻止分泌。因此,导致Yop蛋白III型分泌的信号似乎编码在它们的信使RNA中,而不是肽序列中。