Glass C K, Holloway J M, Devary O V, Rosenfeld M G
Eukaryotic Regulatory Biology Program, School of Medicine, University of California, San Diego, La Jolla 92093-0613.
Cell. 1988 Jul 29;54(3):313-23. doi: 10.1016/0092-8674(88)90194-8.
We report that the thyroid hormone (T3) receptor binds to DNA recognition sequences that are variations of the palindromic motif 5'-TCAGGTCA.TGACCTGA-3', resulting in transcriptional activation in vivo. This sequence is identical to the vitellogenin A2 estrogen response element except for the absence of 3 bp at the center of dyad symmetry, which we have termed a "gap." The T3 receptor binds to estrogen response elements with high affinity in vitro, as well as to variations of the same sequence containing gaps of 1-6 bp. The T3 receptor not only fails to activate transcription from estrogen response elements in vivo, but inhibits estrogen-dependent transactivation. We propose that the T3 receptor binds to estrogen response elements in a transcriptionally inactive form and competes for estrogen receptor binding, resulting in a net decrease in gene expression. These data reveal that only a subset of T3 receptor DNA-binding elements function as T3 response elements.
我们报告称,甲状腺激素(T3)受体与DNA识别序列结合,这些序列是回文基序5'-TCAGGTCA.TGACCTGA-3'的变体,在体内导致转录激活。该序列与卵黄蛋白原A2雌激素反应元件相同,只是在二元对称中心缺少3个碱基对,我们将其称为“间隙”。T3受体在体外与雌激素反应元件具有高亲和力结合,也与包含1-6个碱基对间隙的相同序列变体结合。T3受体不仅在体内不能激活雌激素反应元件的转录,反而抑制雌激素依赖性反式激活。我们提出,T3受体以转录无活性形式与雌激素反应元件结合,并竞争雌激素受体结合,导致基因表达净减少。这些数据表明,只有一部分T3受体DNA结合元件作为T3反应元件发挥作用。