Becker P B, Rabindran S K, Wu C
Laboratory of Biochemistry, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1991 May 15;88(10):4109-13. doi: 10.1073/pnas.88.10.4109.
To investigate the mechanisms of transcriptional regulation of Drosophila heat shock genes we studied the activity of a heat shock promoter in vitro after reconstitution into chromatin. Increasing the duration of nucleosome assembly progressively inactivated a plasmid template when it was transcribed with extracts of either unshocked or heat-shocked Drosophila embryos, despite induction of the transcriptional activator heat shock factor. Addition of the general transcription factor IID (TFIID) before nucleosome assembly did not significantly relieve nucleosomal inhibition, but TFIID potentiated the promoter to be responsive to activation by heat shock factor in the heat shock transcription extract. The potentiation by TFIID could be related to the nucleosome-free, hypersensitive state of heat shock promoters previously observed in vivo before heat shock induction and may be necessitated by the need to expedite activation of heat shock genes in response to environmental stress.
为了研究果蝇热休克基因的转录调控机制,我们在体外将一个热休克启动子重构成染色质后,对其活性进行了研究。当用未受冲击或热休克的果蝇胚胎提取物进行转录时,尽管转录激活因子热休克因子被诱导,但逐渐增加核小体组装的持续时间会使质粒模板逐渐失活。在核小体组装之前添加通用转录因子IID(TFIID)并没有显著缓解核小体抑制作用,但TFIID增强了启动子对热休克转录提取物中热休克因子激活的反应性。TFIID的增强作用可能与热休克启动子在热休克诱导前在体内观察到的无核小体、超敏状态有关,并且可能是为了加快热休克基因对环境应激的激活而必需的。