首页> 外文期刊>Molecular and Cellular Endocrinology >Pituitary NR4A1 is negatively regulated by thyroid hormone without direct binding of thyroid hormone receptors on the gene
【24h】

Pituitary NR4A1 is negatively regulated by thyroid hormone without direct binding of thyroid hormone receptors on the gene

机译:垂体NR4A1被甲状腺激素对甲状腺激素受体的直接结合进行了负面调节

获取原文
获取原文并翻译 | 示例
           

摘要

We previously reported that TRH stimulated pituitary TSH beta gene expression via an immediate increase in NR4A1 in thyrotrophs. We demonstrated that NR4A1 mRNA levels are regulated by thyroid hormone. Pituitary NR4A1 mRNA levels were decreased in mice injected with L-T4. NR4A1 promoter activity was increased by the overexpression of TR beta s, and these increases were decreased by T3, and the -27 similar to+152 bp region was responsible for these changes in vitro. An EMSA showed the lack of TR beta s-isoforms binding, and a ChIP assay demonstrated the recruitment of TR beta s and NCoR in the -147 similar to+148 bp region in the absence of T3, whereas T3 induced their release. Experiments on the overexpression and knockdown of NCoR, and using the mutant TRs supported the involvement of NCoR in the TR-induced stimulation. These results demonstrate that thyroid hormone down-regulated basal NR4A1 mRNA levels in the pituitary, and the direct binding of TR was not required. (C) 2017 Elsevier B.V. All rights reserved.
机译:我们以前报道过TRH刺激垂体TSHβ基因表达,通过立即增加NR4A1在替代术中。我们证明NR4A1 mRNA水平由甲状腺激素调节。用L-T4注入的小鼠中垂体NR4A1 mRNA水平降低。通过TRβS的过表达增加NR4A1启动子活性,通过T3降低这些增加,与+ 152bp区域类似的-27次对这些变化负责这些变化。 EMSA表明缺乏TRβS-同种型结合,并且在不存在T3的情况下,芯片测定证明了在-147中的TRβS和Ncor募集,而T3诱导其释放。 NCOR过表达和敲低的实验,并使用突变TRS支持NCOR在TR诱导的刺激中的参与。这些结果表明,脑垂体中甲状腺激素下调的基础NR4A1 mRNA水平,并且不需要TR的直接结合。 (c)2017 Elsevier B.v.保留所有权利。

著录项

  • 来源
  • 作者单位

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

    Gunma Univ Grad Sch Med Dept Med &

    Mol Sci 3-39-15 Showa Machi Maebashi Gumma 3718511 Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 内分泌腺疾病及代谢病;
  • 关键词

    NR4A1; Thyroid hormone; Thyroid hormone receptor 13; Pituitary; NCoR;

    机译:NR4A1;甲状腺激素;甲状腺激素受体13;垂体;ncor;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号