Sato Yu, Kimura Hiroyuki
Department of Environment and Energy Systems, Graduate School of Science and Technology, Shizuoka University, Shizuoka, 422-8529, Japan.
Department of Geosciences, Faculty of Science, Shizuoka University, 836 Oya, Suruga-ku, Shizuoka, 422-8529, Japan.
Antonie Van Leeuwenhoek. 2019 Feb;112(2):187-201. doi: 10.1007/s10482-018-1144-3. Epub 2018 Aug 20.
Haloarcula strains, which are halophilic archaea, harbour two to three copies of 16S rRNA genes (rrsA, rrsB and rrsC) in their genomes. While rrsB and rrsC (rrsBC) show almost identical sequences, rrsA shows 4-6% sequence difference and 1-3% guanine-plus-cytosine content (P) difference compared to rrsBC. Based on the strong correlation between the P of 16S rRNA genes and the growth temperatures of the prokaryotes, we hypothesised that high-PrrsA and low-PrrsBC are expressed at high and low temperatures, respectively. To verify the hypothesis, we performed sequence analyses and expression surveys of each 16S rRNA gene in eight Haloarcula strains. The secondary structure prediction of the 16S rRNA via computer simulation showed that the structural stability of 16S rRNAs transcribed from rrsA was higher than that of 16S rRNAs transcribed from rrsBC. We measured expression levels of rrsA and rrsBC under various temperature conditions by reverse-transcriptase quantitative PCR. The expression ratio of high-PrrsA to low-PrrsBC increased with cultivation temperatures in seven of eight Haloarcula strains. Our results suggest that the transcription of high-PrrsA and low-PrrsBC may be regulated in response to environmental temperature, and that 16S rRNAs transcribed from high-PrrsA function under high temperature conditions close to the maximum growth temperature.
嗜盐古菌盐盒菌属菌株的基因组中含有两到三个16S rRNA基因拷贝(rrsA、rrsB和rrsC)。虽然rrsB和rrsC(rrsBC)的序列几乎相同,但与rrsBC相比,rrsA的序列差异为4-6%,鸟嘌呤加胞嘧啶含量(P)差异为1-3%。基于16S rRNA基因的P与原核生物生长温度之间的强相关性,我们推测高P的rrsA和低P的rrsBC分别在高温和低温下表达。为了验证这一假设,我们对8株盐盒菌属菌株的每个16S rRNA基因进行了序列分析和表达调查。通过计算机模拟对16S rRNA的二级结构预测表明,从rrsA转录的16S rRNA的结构稳定性高于从rrsBC转录的16S rRNA。我们通过逆转录定量PCR测量了各种温度条件下rrsA和rrsBC的表达水平。在8株盐盒菌属菌株中的7株中,高P的rrsA与低P的rrsBC的表达比例随培养温度的升高而增加。我们的结果表明,高P的rrsA和低P的rrsBC的转录可能受环境温度的调节,并且从高P的rrsA转录的16S rRNA在接近最高生长温度的高温条件下起作用。