首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >The orphan nuclear hormone receptor ERRβ controls rod photoreceptor survival
【24h】

The orphan nuclear hormone receptor ERRβ controls rod photoreceptor survival

机译:孤儿核激素受体ERRβ控制棒状感光细胞的存活

获取原文
获取原文并翻译 | 示例
           

摘要

Mutation of rod photoreceptor-enriched transcription factors is a major cause of inherited blindness. We identified the orphan nuclear hormone receptor estrogen-related receptor p (ERRβ) as selectively expressed in rod photoreceptors. Overexpression of ERRfi induces expression of rod-specific genes in retinas of wild-type as well as Nrl~(-/-) mice, which lack rod photoreceptors. Mutation of ERRβ results in dysfunction and degeneration of rods, whereas inverse agonists of ERRβ trigger rapid rod degeneration, which is rescued by constitutively active mutants of ERRβ. ERRβ coordinates expression of multiple genes that are rate-limiting regulators of ATP generation and consumption in photoreceptors. Furthermore, enhancing ERRβ activity rescues photoreceptor defects that result from loss of the photoreceptor-specif ic transcription factor Crx. Our findings demonstrate that ERRfi is a critical regulator of rod photoreceptor function and survival, and suggest that ERRfi agonists may be useful in the treatment of certain retinal dystrophies.
机译:杆感光细胞富含转录因子的突变是遗传性失明的主要原因。我们确定孤儿核激素受体雌激素相关受体p(ERRβ)在杆感光细胞中选择性表达。 ERRfi的过表达诱导野生型以及Nrl〜(-/-)小鼠缺乏视杆感光器的视网膜中视杆特异性基因的表达。 ERRβ的突变会导致杆的功能障碍和变性,而ERRβ的反向激动剂会引起杆的快速变性,这可由ERRβ的组成型活性突变体挽救。 ERRβ协调多个基因的表达,这些基因是光感受器中ATP产生和消耗的限速调节剂。此外,增强ERRβ活性可以挽救因感光细胞特异性转录因子Crx缺失而引起的感光细胞缺陷。我们的研究结果表明,ERRfi是杆感光细胞功能和生存的关键调节器,并表明ERRfi激动剂可能在某些视网膜营养不良的治疗中有用。

著录项

  • 来源
  • 作者单位

    Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287;

    rnDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110;

    rnDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287;

    rnDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287;

    rnDepartment of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305-5307;

    rnDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287;

    rnDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287;

    rnDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110 Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110;

    rnDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21287 Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287 Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, MD 21287 Center for High-Throughput Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21287 lnstitute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21287;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    crx; ligand; neurodegeneration; retina; development;

    机译:crx;配体神经变性视网膜发展;

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