Palmer Sara R, Burne Robert A
Department of Oral Biology, College of Dentistry, University of Florida, Gainesville, FL, 32610, USA.
Mol Microbiol. 2015 Oct;98(2):302-17. doi: 10.1111/mmi.13122. Epub 2015 Sep 4.
A unique 373 bp region (igr66) between grpE and dnaK of Streptococcus mutans lacks a promoter but is required for optimal production of DnaK. Northern blotting using probes specific to hrcA, igr66 or dnaK revealed multiple transcripts produced from the dnaK operon and 5'-RACE mapped 5' termini of multiple dnaK transcripts within igr66. One product mapped to a predicted 5'-SL (stem-loop) and two others mapped just 5' to Shine-Dalgarno (SD)-like sequences located immediately upstream to dnaK and to a predicted SL 120 bp upstream of the dnaK start codon (3'-SL). A collection of cat reporter-gene strains containing mutant derivatives of igr66 were engineered. Chloramphenicol acetyltransferase (CAT) activity varied greatly between strains, but there were no correlative changes in cat mRNA levels. Interestingly, mutations introduced into the SD-like sequences 5' to the 3'-SL resulted in an 83-98% decrease in CAT activity. Markerless point mutations introduced upstream of dnaK in the SD-like sequences impaired growth at elevated temperatures and resulted in up to a 40% decrease in DnaK protein after heat shock. Collectively, these results indicate processing within igr66 enhances translation in a temperature dependent manner via non-canonical ribosome binding sites positioned >120 bp upstream of dnaK.
变形链球菌的grpE和dnaK之间一个独特的373 bp区域(igr66)缺乏启动子,但对DnaK的最佳产生是必需的。使用针对hrcA、igr66或dnaK的特异性探针进行Northern印迹分析,揭示了从dnaK操纵子产生的多个转录本,并且5'-RACE将多个dnaK转录本的5'末端定位在igr66内。一个产物定位到一个预测的5'-茎环(stem-loop),另外两个产物定位到紧邻dnaK上游的类似Shine-Dalgarno(SD)序列的5'端以及dnaK起始密码子上游120 bp处的一个预测茎环(3'-SL)。构建了一系列含有igr66突变衍生物的cat报告基因菌株。氯霉素乙酰转移酶(CAT)活性在不同菌株之间差异很大,但cat mRNA水平没有相关变化。有趣的是,在3'-SL 5'端的类似SD序列中引入的突变导致CAT活性降低83 - 98%。在类似SD序列中dnaK上游引入的无标记点突变损害了在高温下的生长,并导致热休克后DnaK蛋白最多减少40%。总的来说,这些结果表明igr66内的加工通过位于dnaK上游>120 bp的非经典核糖体结合位点以温度依赖的方式增强翻译。