Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, United States.
Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, United States.
Mol Cell Endocrinol. 2017 Dec 15;458:127-135. doi: 10.1016/j.mce.2017.03.001. Epub 2017 Mar 10.
Thyroid hormones are a critical regulator of mammalian physiology. Much of their action is due to effects in the nucleus where T engages thyroid hormone receptor isoforms to mediate its effects. In order to function properly the TR isoforms must be recruited to regulatory sequences within genes that they up-regulate. On these positive regulated target genes the TR can activate or repress depending upon whether the receptor is bound to T or not and the type of co-regulatory proteins present in that cell type. In contrast to T mediated activation, the mechanism by which the TR represses transcription in the presence of T remains unclear. Herein we will review the components of the transcriptional response to T within the nucleus and attempt to highlight the outstanding questions in the field.
甲状腺激素是哺乳动物生理学的关键调节因子。它们的作用很大程度上归因于细胞核中的作用,T 结合甲状腺激素受体异构体来介导其作用。为了正常发挥功能,TR 异构体必须被招募到它们上调的基因的调节序列中。在这些正调控的靶基因上,TR 可以根据受体是否与 T 结合以及该细胞类型中存在的共调节蛋白的类型激活或抑制转录。与 T 介导的激活不同,在存在 T 的情况下 TR 抑制转录的机制尚不清楚。本文将综述核内 T 介导的转录反应的组成部分,并试图突出该领域的悬而未决的问题。