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核受体通过染色质重塑和组蛋白修饰介导基因调控。

Nuclear receptor mediated gene regulation through chromatin remodeling and histone modifications.

作者信息

Kishimoto Masahiko, Fujiki Ryoji, Takezawa Shinichiro, Sasaki Yasumasa, Nakamura Takashi, Yamaoka Kazuyoshi, Kitagawa Hirochika, Kato Shigeaki

机构信息

Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan.

出版信息

Endocr J. 2006 Apr;53(2):157-72. doi: 10.1507/endocrj.53.157.

Abstract

Nuclear steroid/thyroid vitamin A/D receptor genes form a gene superfamily and encode DNA-binding transcription factors that control the transcription of target genes in a ligand-dependent manner. It has become clear that chromatin remodeling and the modification of histones, the main components of chromatin, play crucial roles in gene transcription, and many distinct classes of NR-interacting co-regulators have been identified that perform significant roles in gene transcription. Since NR dysfunction can lead to the onset or progression of endocrine disease, elucidation of the mechanisms of gene regulation mediated by NRs, as well as the identification and characterization of co-regulator complexes (especially chromatin remodeling and histone-modifying complexes), is essential not only for better understanding of NR ligand function, but also for pathophysiological studies and the development of therapeutic interventions in humans.

摘要

核类固醇/甲状腺维生素A/D受体基因构成一个基因超家族,并编码以配体依赖方式控制靶基因转录的DNA结合转录因子。现已明确,染色质重塑以及染色质主要成分组蛋白的修饰在基因转录中起关键作用,并且已鉴定出许多不同类别的与核受体相互作用的共调节因子,它们在基因转录中发挥重要作用。由于核受体功能障碍可导致内分泌疾病的发生或进展,阐明由核受体介导的基因调控机制,以及鉴定和表征共调节因子复合物(尤其是染色质重塑和组蛋白修饰复合物),不仅对于更好地理解核受体配体功能至关重要,而且对于人类病理生理学研究和治疗干预的开发也必不可少。

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