Brückner R, Matzura H
EMBO J. 1985 Sep;4(9):2295-300. doi: 10.1002/j.1460-2075.1985.tb03929.x.
Analyses of deletion mutants of the gene for chloramphenicol (Cm) acetyltransferase (CAT) carried by the staphylococcal plasmid pUB112 revealed a regulatory region, which is indispensable for Cm-inducible cat gene expression, located 70 bp in front of the CAT-coding sequence. This region consists of a possible ribosome binding site followed by an open reading frame coding for a peptide of nine amino acids and overlaps partially with an inverted repeat capable of forming a stem-loop structure. Deletion of the ribosome binding site and of parts of the open reading frame abolishes inducibility and results in a low-level cat gene expression, if the inverted repeat remains intact. Deletion of the 5' part of the possible stem leads to high-level constitutive CAT synthesis. The inverted repeat, therefore, exhibits negative control on cat gene expression whereas the preceding ribosome binding site is needed to enhance CAT synthesis in the presence of an inducer. These results suggest that translation of a leader peptide is a prerequisite for Cm-induced cat gene expression and that ribosome stalling on cat leader mRNA caused by Cm opens the stem-loop structure thereby releasing its negative effect on CAT synthesis.
对葡萄球菌质粒pUB112携带的氯霉素(Cm)乙酰转移酶(CAT)基因缺失突变体的分析揭示了一个调控区域,该区域位于CAT编码序列前方70 bp处,对Cm诱导的cat基因表达不可或缺。该区域由一个可能的核糖体结合位点和一个编码九个氨基酸肽段的开放阅读框组成,并且与一个能够形成茎环结构的反向重复序列部分重叠。如果反向重复序列保持完整,删除核糖体结合位点和部分开放阅读框会消除诱导性,并导致cat基因低水平表达。删除可能茎环结构的5'部分会导致高水平的组成型CAT合成。因此,反向重复序列对cat基因表达具有负调控作用,而前面的核糖体结合位点则是在诱导剂存在下增强CAT合成所必需的。这些结果表明,前导肽的翻译是Cm诱导的cat基因表达的先决条件,并且由Cm导致的cat前导mRNA上的核糖体停滞会打开茎环结构,从而消除其对CAT合成的负面影响。