Glass C K, Lipkin S M, Devary O V, Rosenfeld M G
Eukaryotic Regulatory Biology Program Center for Molecular Genetics, University of California, San Diego, La Jolla 92093-0613.
Cell. 1989 Nov 17;59(4):697-708. doi: 10.1016/0092-8674(89)90016-0.
We present evidence that the human thyroid hormone receptor forms a heterodimer with the human retinoic acid receptor. This interaction results in a cooperative increase in binding of the alpha retinoic acid receptor to a subset of thyroid hormone response elements. Mutations within the DNA binding domain or near the C-terminus abolish either receptor's ability to interact cooperatively on these elements. The thyroid hormone-retinoic acid receptor heterodimer exhibits novel transcriptional properties in that coexpression of both receptors at low levels in Green monkey kidney (CV1) cells results in a positive transcriptional effect on promoters containing a palindromic thyroid hormone response element, but has a surprisingly negative effect on a thyroid hormone response element derived from the alpha myosin heavy chain gene. These results suggest that by forming heterodimers, more elab-orate control of transcription can be achieved by creating receptor combinations with differing activities.
我们提供的证据表明,人类甲状腺激素受体与人类视黄酸受体形成异源二聚体。这种相互作用导致α视黄酸受体与一部分甲状腺激素反应元件的结合协同增加。DNA结合结构域内或靠近C端的突变会消除任一受体在这些元件上协同相互作用的能力。甲状腺激素 - 视黄酸受体异源二聚体表现出新颖的转录特性,即两种受体在绿猴肾(CV1)细胞中低水平共表达时,对含有回文甲状腺激素反应元件的启动子产生正向转录作用,但对源自α肌球蛋白重链基因的甲状腺激素反应元件却产生惊人的负向作用。这些结果表明,通过形成异源二聚体,可以通过创建具有不同活性的受体组合来实现对转录更精细的调控。