Nagai H, Yuzawa H, Yura T
Institute for Virus Research, Kyoto University, Japan.
Biochimie. 1991 Dec;73(12):1473-9. doi: 10.1016/0300-9084(91)90180-9.
When cells of E coli are transferred from 30 to 42 degrees C, the cellular level of sigma 32 (rpoH gene product) increases transiently, resulting in increased transcription of a set of heat shock genes. Both increased synthesis and increased stability of sigma 32 contribute to transient accumulation of sigma 32. Evidence suggests that synthesis of sigma 32 is enhanced primarily at the level of rpoH translation. We have constructed and examined the expression of deletion derivatives of rpoH-lacZ gene fusion at 30 degrees C and after shift to 42 degrees C. It was revealed that two cis-acting sequences within the rpoH coding region are involved in thermal regulation of fusion protein synthesis. One region immediately downstream of the initiation codon is required for high level expression, whereas the other internal region is involved in repression at low temperature. Thus, these regions act as positive and negative cis-elements in thermal regulation of rpoH translation. The rpoH mRNA secondary structure model suggesting an interplay between the two regions has been proposed to account for the temperature-induced sigma 32 synthesis as a primary cellular response to the heat shock stress.
当大肠杆菌细胞从30℃转移至42℃时,σ32(rpoH基因产物)的细胞水平会短暂升高,导致一组热休克基因的转录增加。σ32合成的增加和稳定性的提高都有助于其短暂积累。有证据表明,σ32的合成主要在rpoH翻译水平上增强。我们构建并检测了rpoH-lacZ基因融合缺失衍生物在30℃以及转移至42℃后的表达情况。结果显示,rpoH编码区内的两个顺式作用序列参与了融合蛋白合成的热调节。起始密码子下游紧邻的一个区域是高水平表达所必需的,而另一个内部区域则参与低温下的抑制作用。因此,这些区域在rpoH翻译的热调节中分别作为正性和顺式元件起作用。有人提出了rpoH mRNA二级结构模型,表明这两个区域之间存在相互作用,以此来解释温度诱导的σ32合成是细胞对热休克应激的主要反应。