Weiner J, Zimmerman C-U, Göhlmann H W H, Herrmann R
Zentrum für Molekulare Biologie Heidelberg, Universität Heidelberg, 69120 Heidelberg, Germany.
Nucleic Acids Res. 2003 Nov 1;31(21):6306-20. doi: 10.1093/nar/gkg841.
Applying microarray technology, we have investigated the transcriptome of the small bacterium Mycoplasma pneumoniae grown at three different temperature conditions: 32, 37 and 32 degrees C followed by a heat shock for 15 min at 43 degrees C, before isolating the RNA. From 688 proposed open-reading frames, 676 were investigated and 564 were found to be expressed (P < 0.001; 606 with P < 0.01) and at least 33 (P < 0.001; 77 at P < 0.01) regulated. By quantitative real-time PCR of selected mRNA species, the expression data could be linked to absolute molecule numbers. We found M.pneumoniae to be regulated at the transcriptional level. Forty-seven genes were found to be significantly up-regulated after heat shock (P < 0.01). Among those were the conserved heat shock genes like dnaK, lonA and clpB, but also several genes coding for ribosomal proteins and 10 genes of unassigned functions. In addition, 30 genes were found to be down-regulated under the applied heat shock conditions. Further more, we have compared different methods of cDNA synthesis (random hexamer versus gene-specific primers, different RNA concentrations) and various normalization strategies of the raw microarray data.
应用微阵列技术,我们研究了在三种不同温度条件下生长的小型细菌肺炎支原体的转录组:32℃、37℃以及32℃培养后在43℃热激15分钟,然后分离RNA。在688个预测的开放阅读框中,研究了676个,发现564个表达(P < 0.001;P < 0.01时为606个),并且至少33个(P < 0.001;P < 0.01时为77个)受到调控。通过对选定mRNA种类进行定量实时PCR,可将表达数据与绝对分子数联系起来。我们发现肺炎支原体在转录水平受到调控。热激后有47个基因显著上调(P < 0.01)。其中包括保守的热激基因如dnaK、lonA和clpB,还有几个编码核糖体蛋白的基因以及10个功能未明确的基因。此外,发现在所应用的热激条件下有30个基因下调。此外,我们比较了cDNA合成的不同方法(随机六聚体与基因特异性引物、不同RNA浓度)以及原始微阵列数据的各种归一化策略。