Burcin M, Köhne A C, Runge D, Steiner C, Renkawitz R
Genetisches Institut der Justus-Liebig-Universität Giessen, Germany.
Semin Cancer Biol. 1994 Oct;5(5):337-46.
Members of the steroid receptor superfamily, like other transcription factors, can function as transcriptional inducers as well as repressors of transcription. The mechanisms by which repression is achieved seem to be specific for the factors and regulatory sequences involved. Silencing activity is conferred by the DNA bound v-ERBA, which is able to repress the activity of a complete or of a minimal promoter. Removal of the T3 or RA ligands converts the activated form of TR or RAR into a silencing conformation. Ligand-free TR, RAR or v-ERBA synergize with the DNA-bound negative protein 1 (NeP1) in a specific silencer sequence. In contrast to silencing, competitive repression is seen for specific negative hormone response elements. These elements are characterized by the presence of binding sites for other transcription factors.
类固醇受体超家族的成员与其他转录因子一样,既可以作为转录诱导剂,也可以作为转录抑制剂发挥作用。实现抑制的机制似乎因所涉及的因子和调控序列而异。沉默活性由与DNA结合的v-ERBA赋予,它能够抑制完整或最小启动子的活性。去除T3或RA配体可将TR或RAR的激活形式转变为沉默构象。无配体的TR、RAR或v-ERBA在特定的沉默子序列中与结合DNA的负性蛋白1(NeP1)协同作用。与沉默不同,在特定的负性激素反应元件上可观察到竞争性抑制。这些元件的特征是存在其他转录因子的结合位点。