作者: Daniel M. Cohen , David J. Steger
DOI: 10.1016/J.TEM.2017.04.001
关键词: Functional genomics 、 Nuclear receptor coactivator 2 、 Transcription factor 、 Neuron-derived orphan receptor 1 、 Biology 、 Glucocorticoid receptor 、 Nuclear receptor co-repressor 1 、 Cell biology 、 Genetics 、 Regulation of gene expression 、 Nuclear receptor
摘要: Unlocking the therapeutic potential of glucocorticoid receptor (GR) has motivated a search for small molecules that selectively modulate its ability to activate or repress gene transcription. Recently, breakthrough studies in field genomics have reinvigorated debate over longstanding transcriptional models explaining how GR controls tissue-specific expression. Here, we highlight these genomic with dual goals advancing understanding nuclear receptor-mediated transcription and stimulating thought on development anti-inflammatory immunosuppressive ligands reduced harmful effects metabolism.