Transcriptional repression by nuclear hormone receptors
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作者:
Hu, X
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机构:
Univ Penn, Med Ctr, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USAUniv Penn, Med Ctr, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
Hu, X
[1
]
Lazar, MA
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机构:Univ Penn, Med Ctr, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
Lazar, MA
机构:
[1] Univ Penn, Med Ctr, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
[2] Univ Penn, Med Ctr, Dept Genet, Philadelphia, PA 19104 USA
[3] Univ Penn, Med Ctr, Penn Diabet Ctr, Philadelphia, PA 19104 USA
Repression by nuclear receptor plays important roles in a cute promyelocytic leukemia and other diseases. nuclear receptor corepressor (N-CoR) and SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) are corepressor proteins whose modular structure facilitates receptor interaction as well as translation of repression signals involving histone deacetylation, alterations in chromatin structure and direct interactions with the basal transcription machinery. Interactions between nuclear receptors and corepressor complexes have multiple determinants. This allows regulation, and potentially therapeutic manipulation, of receptor, corepressor, cell-type and target-gene specificity.