Zimarino V, Wilson S, Wu C
Laboratory of Biochemistry, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Science. 1990 Aug 3;249(4968):546-9. doi: 10.1126/science.2200124.
Eukaryotic cells respond to elevated temperatures by rapidly activating the expression of heat shock genes. Central to this activation is heat shock-inducible binding of the transcriptional activator, termed heat shock factor (HSF), to common regulatory elements, which are located upstream of all heat shock genes. The DNA binding activity of the inactive form of Drosophila HSF was induced in vitro by treatment with polyclonal antibodies to the purified, in vivo-activated factor. This finding, together with observations that high temperature and low pH activate HSF binding in vitro, suggests that the inactive form of HSF can directly recognize and transduce the heat shock signal without undergoing a covalent modification of protein structure.
真核细胞通过迅速激活热休克基因的表达来应对温度升高。这种激活的核心是转录激活因子热休克因子(HSF)与所有热休克基因上游的共同调控元件进行热休克诱导性结合。用针对纯化的、体内激活形式的多克隆抗体处理,可在体外诱导果蝇HSF无活性形式的DNA结合活性。这一发现,连同高温和低pH在体外激活HSF结合的观察结果,表明HSF的无活性形式可以直接识别并转导热休克信号,而无需经历蛋白质结构的共价修饰。