Morgan J E, Whitlock J P
Department of Pharmacology, Stanford University School of Medicine, CA 94305-5332.
Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11622-6. doi: 10.1073/pnas.89.23.11622.
In mouse hepatoma cells, both the regulatory and the transcribed regions of the cyp1a1 gene assume a nucleosomal configuration when the gene is silent; two nucleosomes occupy specific sites at the transcriptional promoter. Activation of transcription by 2,3,7,8-tetrachlorodibenzo-p-dioxin is accompanied by changes in chromatin structure, which depend upon a functional aromatic hydrocarbon (Ah) receptor. In the transcribed region of the gene, nucleosome disruption occurs as a consequence of RNA elongation. In contrast, at the promoter, loss of positioned nucleosome sis independent of transcription and represents an event in the mechanism by which the liganded Ah receptor enhances transcriptional initiation.
在小鼠肝癌细胞中,当cyp1a1基因沉默时,其调控区和转录区均呈现核小体结构;两个核小体占据转录启动子的特定位点。2,3,7,8-四氯二苯并对二恶英激活转录时伴随着染色质结构的变化,这取决于功能性芳烃(Ah)受体。在基因的转录区,核小体的破坏是RNA延伸的结果。相反,在启动子处,定位核小体的丢失与转录无关,代表了配体结合的Ah受体增强转录起始机制中的一个事件。