Taylor W E, Straus D B, Grossman A D, Burton Z F, Gross C A, Burgess R R
Cell. 1984 Sep;38(2):371-81. doi: 10.1016/0092-8674(84)90492-6.
The rpoD gene encoding the sigma subunit of E. coli RNA polymerase is cotranscribed with rpsU and dnaG, encoding ribosomal protein S21 and DNA primase, respectively. After temperature upshift, a heat shock promoter (Phs) located within dnaG is transiently induced, causing increased transcription of rpoD. The extent of induction is sufficient to account for the heat shock response of sigma synthesis. The initiation site of this promoter was located about 360 bp upstream of rpoD by promoter cloning and S1 nuclease mapping. Plasmid deletions generated with Bal 31 nuclease show that the DNA sequence CTGCCACCC in the -44 to -36 region of this promoter is necessary for its heat shock activity. Heat induction of transcription from Phs is under the control of HtpR, a positive regulator of the heat shock response.
编码大肠杆菌RNA聚合酶σ亚基的rpoD基因与分别编码核糖体蛋白S21和DNA引发酶的rpsU和dnaG共转录。温度升高后,位于dnaG内的一个热休克启动子(Phs)被短暂诱导,导致rpoD转录增加。诱导程度足以解释σ亚基合成的热休克反应。通过启动子克隆和S1核酸酶图谱分析,该启动子的起始位点位于rpoD上游约360 bp处。用Bal 31核酸酶产生的质粒缺失表明,该启动子-44至-36区域的DNA序列CTGCCACCC对其热休克活性是必需的。来自Phs的转录热诱导受热休克反应的正调控因子HtpR的控制。