Tagami T, Kopp P, Johnson W, Arseven O K, Jameson J L
Division of Endocrinology, Metabolism, and Molecular Medicine, Northwestern University Medical School, Chicago, Illinois 60611, USA.
Endocrinology. 1998 May;139(5):2535-44. doi: 10.1210/endo.139.5.6011.
The thyroid hormone receptor splice variant, alpha2, is unable to bind thyroid hormone (T3) and has been proposed to function as an endogenous inhibitor of T3 action. In this report, we examined further the DNA sequence requirements for alpha2 binding to thyroid hormone response elements (TREs) in an attempt to identify response elements that mediate potent inhibition by alpha2. Heterodimers of alpha2 and retinoid X receptor were found to bind to a subset of TREs (DR4, direct repeats spaced by 4 bp) in which selected flanking and spacer sequences enhanced interactions with the AGGTCA core binding sequence. Despite the optimization of the TRE-binding sites, alpha2 remained a weak dominant negative inhibitor of TRE-driven transcription. A promoter interference assay was also developed for testing inhibition by alpha2. In these studies, alpha2 blocked gene transcription, but it required cotransfected retinoid X receptor, and it was not as potent as unliganded thyroid hormone receptors. These results led to the hypothesis that alpha2 might be deficient in interactions with nuclear receptor corepressors. Consistent with this view, alpha2 did not silence basal transcription in its native form or when linked to Gal4. Alpha2 also failed to interact with corepressors (NCoR and SMRT) in both gel shift assays and mammalian two-hybrid assays. We conclude that alpha2 is a weak antagonist of thyroid hormone action because it binds weakly to a limited repertoire of response elements, and it does not interact with corepressors. Thus, alpha2 may be able to compete with thyroid hormone receptors for binding to a limited group of target sites, but it is not able to actively inhibit transcription.
甲状腺激素受体剪接变体α2无法结合甲状腺激素(T3),有人提出它可作为T3作用的内源性抑制剂。在本报告中,我们进一步研究了α2与甲状腺激素反应元件(TREs)结合的DNA序列要求,试图鉴定介导α2强效抑制作用的反应元件。发现α2与视黄酸X受体的异二聚体可结合到一部分TREs(DR4,间隔4个碱基对的直接重复序列)上,其中特定的侧翼和间隔序列增强了与AGGTCA核心结合序列的相互作用。尽管优化了TRE结合位点,α2仍然是TRE驱动转录的弱显性负抑制剂。还开发了一种启动子干扰试验来测试α2的抑制作用。在这些研究中,α2阻断基因转录,但它需要共转染视黄酸X受体,并且其效力不如未结合配体的甲状腺激素受体。这些结果导致了这样一种假设,即α2可能在与核受体共抑制因子的相互作用方面存在缺陷。与此观点一致的是,α2无论是以天然形式还是与Gal4连接时,都不能使基础转录沉默。在凝胶迁移试验和哺乳动物双杂交试验中,α2也未能与共抑制因子(NCoR和SMRT)相互作用。我们得出结论,α2是甲状腺激素作用的弱拮抗剂,因为它与有限的一组反应元件结合较弱,并且不与共抑制因子相互作用。因此,α2可能能够与甲状腺激素受体竞争结合有限的一组靶位点,但它不能积极抑制转录。