Skelly S, Coleman T, Fu C F, Brot N, Weissbach H
Roche Institute of Molecular Biology, Roche Research Center, Nutley, NJ 07110.
Proc Natl Acad Sci U S A. 1987 Dec;84(23):8365-9. doi: 10.1073/pnas.84.23.8365.
S-30 extracts from Escherichia coli cells were used to express heat shock (HS) and non-HS genes in vitro in a DNA-directed protein synthesis system. The S-30 extracts prepared from cells that have been shifted to 45 degrees C express HS genes in vitro approximately 8 times better than extracts from cells at 33 degrees C. In contrast, the expression of non-HS genes in extracts from heat-induced cells is only 40% of that seen in extracts from cells at 33 degrees C. These results correlate well with the levels of HS sigma factor and normal sigma factor bound to RNA polymerase. Thus, there was an 8-fold increase in the HS sigma factor and a 60% decrease in the normal sigma factor associated with RNA polymerase at the higher temperature. Part of the increase in the level of the HS sigma factor could be accounted for by a 3-fold increase in the level of HS sigma factor mRNA during heat induction.
用大肠杆菌细胞的S-30提取物在体外DNA指导的蛋白质合成系统中表达热休克(HS)基因和非HS基因。从已转移至45摄氏度的细胞制备的S-30提取物在体外表达HS基因的能力比从33摄氏度细胞制备的提取物高约8倍。相比之下,热诱导细胞提取物中非HS基因的表达仅为33摄氏度细胞提取物中表达的40%。这些结果与结合到RNA聚合酶上的HS σ因子和正常σ因子的水平密切相关。因此,在较高温度下,与RNA聚合酶相关的HS σ因子增加了8倍,正常σ因子减少了60%。HS σ因子水平的部分增加可归因于热诱导期间HS σ因子mRNA水平增加了3倍。